Pure and Applied Chemistry

CrossRef Cited-by Linking

• Bandala Yamir, Reyes-Rangel Gloria, Obregón-Zúñiga Arturo, Cruz-Hernández Carlos, Corzo Gerardo, Juaristi Eusebio: trans -Hexahydrobenzoxazolidinones in the Enantioselective Synthesis of β2 -Amino Acids Containing Proteinogenic Side Chains. Eur. J. Org. Chem. 2014, 2014, 2275. <http://dx.doi.org/10.1002/ejoc.201301834>
• Aursnes M., Tungen J. E., Vik A., Dalli J., Hansen T. V.: Stereoselective synthesis of protectin D1: a potent anti-inflammatory and proresolving lipid mediator. Org. Biomol. Chem. 2014, 12, 432. <http://dx.doi.org/10.1039/c3ob41902a>
• Dias Luiz C., Perez Carla C.: Synthesis of the C4-C17 Fragment of Saliniketals A and B. Eur. J. Org. Chem. 2013, 2013, 2930. <http://dx.doi.org/10.1002/ejoc.201300012>
• Kong Han Il, Gill Monica A., Hrdina Amy H., Crichton Jennifer E., Manthorpe Jeffrey M.: Reactivity of α-trifluoromethanesulfonyl esters, amides and ketones: Decarboxylative allylation, methylation, and enol formation. Journal of Fluorine Chemistry 2013, 153, 151. <http://dx.doi.org/10.1016/j.jfluchem.2013.03.020>
• Li Suhua, Ye Juntao, Yuan Weiming, Ma Shengming: Highly regioselective three-component palladium-catalyzed synthesis of 5-vinyloxazolidin-2-ones from 2,3-allenyl amines, organic iodides, and carbon dioxide. Tetrahedron 2013, 69, 10450. <http://dx.doi.org/10.1016/j.tet.2013.09.087>
• Heravi Majid M., Zadsirjan Vahideh: Oxazolidinones as chiral auxiliaries in asymmetric aldol reactions applied to total synthesis. Tetrahedron: Asymmetry 2013, 24, 1149. <http://dx.doi.org/10.1016/j.tetasy.2013.08.011>
• Ramachandran P. Veeraraghavan, Chanda Prem B.: Overriding effect of temperature over reagent and substrate size for boron-mediated aldol reaction of methyl phenylacetate. Tetrahedron Letters 2013, 54, 5886. <http://dx.doi.org/10.1016/j.tetlet.2013.08.106>
• Flynn Bernard L., Manchala Narasimhulu, Krenske Elizabeth H.: Opposing Auxiliary Conformations Produce the Same Torquoselectivity in an Oxazolidinone-Directed Nazarov Cyclization. J. Am. Chem. Soc. 2013, 135, 9156. <http://dx.doi.org/10.1021/ja4036434>
• Halperin Shira D., Britton Robert: Chlorine, an atom economical auxiliary for asymmetric aldol reactions. Org. Biomol. Chem. 2013, 11, 1702. <http://dx.doi.org/10.1039/c3ob27462d>
• Feng Huangdi, Ermolat'ev Denis S., Song Gonghua, Van der Eycken Erik V.: Synthesis of Oxazolidin-2-ones via a Copper(I)-Catalyzed Tandem Decarboxylative/Carboxylative Cyclization of a Propiolic Acid, a Primary Amine and an Aldehyde. Synth Catal 2012, 354, 505. <http://dx.doi.org/10.1002/adsc.201100608>
• Oishi Shunsuke, Saito Susumu: Double Molecular Recognition with Aminoorganoboron Complexes: Selective Alcoholysis of β-Dicarbonyl Derivatives. Angew. Chem. 2012, 124, 5491. <http://dx.doi.org/10.1002/ange.201200304>
• Oishi Shunsuke, Saito Susumu: Double Molecular Recognition with Aminoorganoboron Complexes: Selective Alcoholysis of β-Dicarbonyl Derivatives. Angew. Chem. Int. Ed. 2012, 51, 5395. <http://dx.doi.org/10.1002/anie.201200304>
• van der Knaap Matthijs, Basalan Fatih, van de Mei Henny C., Busscher Henk J., van der Marel Gijsbert A., Overkleeft Herman S., Overhand Mark: Synthesis and Biological Evaluation of Gramicidin S-Inspired Cyclic Mixed α /β -Peptides. Chemistry & Biodiversity 2012, 9, 2494. <http://dx.doi.org/10.1002/cbdv.201200277>
• Messmer Andreas T., Lippert Katharina M., Steinwand Sabrina, Lerch Eliza-Beth W., Hof Kira, Ley David, Gerbig Dennis, Hausmann Heike, Schreiner Peter R., Bredenbeck Jens: Two-Dimensional Infrared Spectroscopy Reveals the Structure of an Evans Auxiliary Derivative and Its SnCl4 Lewis Acid Complex. Chem. Eur. J. 2012, 18, 14989. <http://dx.doi.org/10.1002/chem.201201583>
• Joosten Antoine, Persson Andreas K. Å., Millet Renaud, Johnson Magnus T., Bäckvall Jan-E.: Palladium(II)-Catalyzed Oxidative Cyclization of Allylic Tosylcarbamates: Scope, Derivatization, and Mechanistic Aspects. Chem. Eur. J. 2012, 18, 15151. <http://dx.doi.org/10.1002/chem.201202359>
• Tietze Lutz F., Schützenmeister Nina, Grube Alexander, Scheffer Timo, Baag Mohammad Merajuddin, Granitzka Markus, Stalke Dietmar: Synthesis of Spinosyn Analogues for Modern Crop Protection. Eur. J. Org. Chem. 2012, 2012, 5748. <http://dx.doi.org/10.1002/ejoc.201200600>
• Ishikawa Takashi, Noritake Hiroto, Totani Kiichiro: Influence of Hyaluronan Environments on the Stereoselectivity of an Aldol Reaction. Jnl Chinese Chemical Soc 2012, 59, 265. <http://dx.doi.org/10.1002/jccs.201100564>
• Tripathy Sibanarayan, Chattopadhyay Angshuman: (R)-2,3-O-Cyclohexylideneglyceraldehyde: a useful template for a simple entry into carbafuranose stereoisomers. Tetrahedron: Asymmetry 2012, 23, 1423. <http://dx.doi.org/10.1016/j.tetasy.2012.09.007>
• Cook Cyril, Liron Frédéric, Guinchard Xavier, Roulland Emmanuel: Study of the Total Synthesis of (−)-Exiguolide. J. Org. Chem. 2012, 77, 6728. <http://dx.doi.org/10.1021/jo301066p>
• Ye Juntao, Li Suhua, Ma Shengming: Palladium-Catalyzed Cyclization Reactions of 2,3-Allenyl Amines with Propargylic Carbonates. Z Org Lett 2012, 14, 2312. <http://dx.doi.org/10.1021/ol3007293>
• Khatik Gopal L., Kumar Varun, Nair Vipin A.: Reversal of Selectivity in Acetate Aldol Reactions of N-Acetyl-(S)-4-isopropyl-1-[(R)-1-phenylethyl]imidazolidin-2-one. Z Org Lett 2012, 14, 2442. <http://dx.doi.org/10.1021/ol300949s>
• Ramachandran P. Veeraraghavan, Chanda Prem B.: Solvent- or Temperature-Controlled Diastereoselective Aldol Reaction of Methyl Phenylacetate. Org. Lett. 2012, 14, 4346. <http://dx.doi.org/10.1021/ol301782s>
• Harada Kenichi, Horiuchi Hiroki, Tanabe Kazuma, Carter Rich G., Esumi Tomoyuki, Kubo Miwa, Hioki Hideaki, Fukuyama Yoshiyasu: Asymmetric synthesis of (−)-chicanine using a highly regioselective intramolecular Mitsunobu reaction and revision of its absolute configuration. Tetrahedron Letters 2011, 52, 3005. <http://dx.doi.org/10.1016/j.tetlet.2011.03.154>
• Kong Han Il, Crichton Jennifer E., Manthorpe Jeffrey M.: Stereoselective synthesis of ambiphilic alkenes via regioselective methylation of α-trifluoromethanesulfonyl carbonyl compounds with trimethylsilyldiazomethane. Tetrahetron Lett 2011, 52, 3714. <http://dx.doi.org/10.1016/j.tetlet.2011.05.015>
• Slade Joel, Liu Hui, Prashad Mahavir, Prasad Kapa: A new synthesis of the orally active renin inhibitor aliskiren. Tetrahedron Letters 2011, 52, 4349. <http://dx.doi.org/10.1016/j.tetlet.2011.06.056>
• Barluenga José, Suero Marcos G., De la Campa Raquel, Flórez Josefa: Enantioselective Synthesis of 4-Hydroxy-2-cyclohexenones through a Multicomponent Cyclization. Angew Chem 2010, 122, 9914. <http://dx.doi.org/10.1002/ange.201004413>
• Flórez Josefa, Barluenga José, Suero Marcos G., De la Campa Raquel: Enantioselective Synthesis of 4-Hydroxy-2-cyclohexenones through a Multicomponent Cyclization. Angew Chem Int Ed 2010, 49, 9720. <http://dx.doi.org/10.1002/anie.201004413>
• Organische Chemie 1981. Nachr Chem Tech Lab 2010, 30, 89. <http://dx.doi.org/10.1002/nadc.19820300204>
• Oh Hong-Se, Kang Han-Young: Total synthesis of neomethymycin and novamethymycin. Tetrahedron 2010, 66, 4307. <http://dx.doi.org/10.1016/j.tet.2010.04.039>
• Chattopadhyay Angshuman, Goswami Dibakar, Dhotare Bhaskar: Crotylation of (R)-2,3-O-cyclohexylideneglyceraldehyde: a simple synthesis of (+)-trans-oak lactone. Tetrahetron Lett 2010, 51, 3893. <http://dx.doi.org/10.1016/j.tetlet.2010.05.070>
• Martin René, Entchev Eugeni V., Kurzchalia Teymuras V., Knölker Hans-Joachim: Steroid hormones controlling the life cycle of the nematode Caenorhabditis elegans: stereoselective synthesis and biology. Org Biomol Chem 2010, 8, 739. <http://dx.doi.org/10.1039/b918488k>
• Marrone Alessandro, Renzetti Andrea, De Maria Paolo, Gérard Stéphane, Sapi Janos, Fontana Antonella, Re Nazzareno: Condensation of β-Diester Titanium Enolates with Carbonyl Substrates: A Combined DFT and Experimental Investigation. Chem. Eur. J. 2009, 15, 11537. <http://dx.doi.org/10.1002/chem.200901595>
• Martin René, Entchev Eugeni V., Däbritz Frank, Kurzchalia Teymuras V., Knölker Hans-Joachim: Synthesis and Hormonal Activity of the (25S)-Cholesten-26-oic Acids - Potent Ligands for the DAF-12 Receptor in Caenorhabditis elegans . Eur J Org Chem 2009, 2009, 3703. <http://dx.doi.org/10.1002/ejoc.200900443>
• TOURWÉ D, COUDER J., CEUSTERS M., MEERT D., BURKS T. F., KRAMER T. H., DAVIS P., KNAPP R., YAMAMURA H. I., LEYSEN J. E.: Synthesis and biological activities of linear and cyclic enkephalin analogues containing a Ψ (E,CH=CH) or Ψ (CH2CH2) isosteric replacement. Int J Peptide Protein Res 2009, 39, 131. <http://dx.doi.org/10.1111/j.1399-3011.1992.tb00782.x>
• Yuan J. Y., Liao X. C., Wang H. M., Tang M. S.: Camphor-based α-bromoketones for the asymmetric darzens reaction: Insights into the mechanism using density functional theory. J Struct Chem 2008, 49, 818. <http://dx.doi.org/10.1007/s10947-008-0144-y>
• Liu Jian, Zhang Ling, He Jinmei, He Liuer, Ma Bowen, Pan Xinfu, She Xuegong: Facile total synthesis of the antimalarial nonenolide. Tet Asymm 2008, 19, 906. <http://dx.doi.org/10.1016/j.tetasy.2008.03.024>
• Reyes-Rangel Gloria, Jiménez-González Erika, Olivares-Romero José Luis, Juaristi Eusebio: Enantioselective synthesis of beta-amino acids using hexahydrobenzoxazolidinones as chiral auxiliaries. Tet Asymm 2008, 19, 2839. <http://dx.doi.org/10.1016/j.tetasy.2008.12.023>
• Martinez-Solorio Dionicio, Jennings Michael P.: Chemoselective TBS deprotection of primary alcohols by means of pyridinium tribromide (Py·Br3) in MeOH. Tetrahetron Lett 2008, 49, 5175. <http://dx.doi.org/10.1016/j.tetlet.2008.06.072>
• Florence Gordon J., Gardner Nicola M., Paterson Ian: Development of practical syntheses of the marine anticancer agents discodermolide and dictyostatin. Nat Prod Rep 2008, 25, 342. <http://dx.doi.org/10.1039/b705661n>
• Martin René, Däbritz Frank, Entchev Eugeni V., Kurzchalia Teymuras V., Knölker Hans-Joachim: Stereoselective synthesis of the hormonally active (25S)-Δ7-dafachronic acid, (25S)-Δ4-dafachronic acid, (25S)-dafachronic acid, and (25S)-cholestenoic acid. Org Biomol Chem 2008, 6, 4293. <http://dx.doi.org/10.1039/b815064h>
• Nakazaki Atsuo, Era Tomohiro, Kobayashi Susumu: Stereocontrolled Total Synthesis of (−)-Gleenol Using Claisen Rearrangement of Sterically Congested Dihydropyran. Chem Lett 2008, 37, 770. <http://dx.doi.org/10.1246/cl.2008.770>
• Nicolaou K. C., Guduru Ramakrishna, Sun Ya-Ping, Banerji Biswadip, Chen David Y.-K.: Total Synthesis of the Originally Proposed and Revised Structures of Palmerolide A. Angew Chem 2007, 119, 6000. <http://dx.doi.org/10.1002/ange.200702243>
• Nicolaou K. C., Guduru Ramakrishna, Sun Ya-Ping, Banerji Biswadip, Chen David Y.-K.: Total Synthesis of the Originally Proposed and Revised Structures of Palmerolide A. Angew Chem Int Ed 2007, 46, 5896. <http://dx.doi.org/10.1002/anie.200702243>
• Tietze Lutz F., Brasche Gordon, Grube Alexander, Böhnke Niels, Stadler Christian: Synthesis of Novel Spinosyn A Analogues by Pd-Mediated Transformations. Chem Eur J 2007, 13, 8543. <http://dx.doi.org/10.1002/chem.200700464>
• Fustero Santos, Piera Julio, Sanz-Cervera Juan F., Bello Paula, Mateu Natalia: Synthesis of a new fluorinated oxazolidinone and its reactivity as a chiral auxiliary in Aldol reactions. J FLUORINE CHEM 2007, 128, 647. <http://dx.doi.org/10.1016/j.jfluchem.2007.03.001>
• Koseki Yuji, Fujino Koji, Takeshita Ai, Sato Hiroto, Nagasaka Tatsuo: The intramolecular tandem Michael/Mannich-type reaction of α,β-unsaturated carbonyl compounds with acyliminium ions provides access to chiral indolizidines. Tet Asymm 2007, 18, 1533. <http://dx.doi.org/10.1016/j.tetasy.2007.06.009>
• Bajpai Reena, Yang Fanglong, Curran Dennis P.: On the structure of the Phytophthora α1 mating hormone: synthesis and comparison of four candidate stereoisomers. Tetrahetron Lett 2007, 48, 7965. <http://dx.doi.org/10.1016/j.tetlet.2007.09.054>
• Beddow James E., Davies Stephen G., Ling Kenneth B., Roberts Paul M., Russell Angela J., Smith Andrew D., Thomson James E.: Asymmetric synthesis of β2-amino acids: 2-substituted-3-aminopropanoic acids from N-acryloyl SuperQuat derivatives. Org Biomol Chem 2007, 5, 2812. <http://dx.doi.org/10.1039/b707689d>
• Drauz Karlheinz, Kleemann Axel, Martens Jürgen: Induktion von Asymmetrie durch Aminosäuren. Angew Chem 2006, 94, 590. <http://dx.doi.org/10.1002/ange.19820940804>
• Seebach Dieter, Prelog Vladimir: Spezifikation des sterischen Verlaufs von asymmetrischen Synthesen. Angew Chem 2006, 94, 696. <http://dx.doi.org/10.1002/ange.19820940904>
• Tietze Lutz F., Brasche Gordon, Stadler Christian, Grube Alexander, Böhnke Niels: Multiple Pd-katalysierte Reaktionen zur Synthese von Analoga des hochpotenten Insektizids Spinosyn A. Angew Chem 2006, 118, 5137. <http://dx.doi.org/10.1002/ange.200601003>
• Tietze Lutz F., Brasche Gordon, Stadler Christian, Grube Alexander, Böhnke Niels: Multiple Palladium-Catalyzed Reactions for the Synthesis of Analogues of the Highly Potent Insecticide Spinosyn A. Angew Chem Int Ed 2006, 45, 5015. <http://dx.doi.org/10.1002/anie.200601003>
• Reyes-Rangel Gloria, Marañón Virginia, Avila-Ortiz C. Gabriela, Anaya de Parrodi Cecilia, Quintero Leticia, Juaristi Eusebio: Enantioselective synthesis of (S)-2-amino-3-phosphonopropionic acid, (S)-AP-3, and (R)-2-amino-4-phosphonobutanoic acid, (R)-AP-4, via diastereoselective azidation of (4R,5R)-trans-N-[(diethoxyphosphoryl)propionyl]- and (4R,5R)-trans-N-[(diethoxyphosphoryl)butanoyl]hexahydrobenzoxazolidin-2-one. Tetrahedron 2006, 62, 8404. <http://dx.doi.org/10.1016/j.tet.2006.06.018>
• Sawant Kailas B., Ding Fei, Jennings Michael P.: An efficient synthesis of the C1–C14 subunit of (−)-lasonolide A via a target oriented β-C-glycoside formation sequence. Tetrahetron Lett 2006, 47, 939. <http://dx.doi.org/10.1016/j.tetlet.2005.11.156>
• Clough John M., Dube Henry, Martin Bruce J., Pattenden Gerald, Reddy K. Srinivasa, Waldron Ian R.: Total synthesis of myxothiazols, novel bis-thiazole ?-methoxyacrylate-based anti-fungal compounds from myxobacteria. Org Biomol Chem 2006, 4, 2906. <http://dx.doi.org/10.1039/b603433k>
• Bull Steven D., Davies Stephen G., Garner A. Christopher, Kruchinin Dennis, Key Min-Suk, Roberts Paul M., Savory Edward D., Smith Andrew D., Thomson James E.: SuperQuat 5,5-dimethyl-4-iso-propyloxazolidin-2-one as a mimic of Evans 4-tert-butyloxazolidin-2-one. Org Biomol Chem 2006, 4, 2945. <http://dx.doi.org/10.1039/b605244d>
• Shin Dong Gyun, Heo Hye Jin, Jun Jong‐Gab: Stereoselective Synthesis of β‐Lactams by Using D‐Mannitol‐Derived Oxazolidin‐2‐one as a Chiral Auxiliary. Synth Common 2005, 35, 845. <http://dx.doi.org/10.1081/SCC-200050961>
• Hodge Mathis B., Olivo Horacio F.: Stereoselective aldol additions of titanium enolates of N-acetyl-4-isopropyl-thiazolidinethione. Tetrahedron 2004, 60, 9397. <http://dx.doi.org/10.1016/j.tet.2004.08.008>
• Ghosh Arun K., Xu Xiaoming: Assignment of Absolute Stereochemistry and Total Synthesis of (−)-Spongidepsin. Org Lett 2004, 6, 2055. <http://dx.doi.org/10.1021/ol049292p>
• Merlo Aloir A., Fernandes Mirele S.: An Efficient Strategy for the Synthesis of Chiral Liquid Crystals Using Evans' Methodology. Synth Common 2003, 33, 1167. <http://dx.doi.org/10.1081/SCC-120017193>
• Palomo Claudio, Oiarbide Mikel, García Jesús M.: The Aldol Addition Reaction: An Old Transformation at Constant Rebirth. Chem Eur J 2002, 8, 36. <http://dx.doi.org/10.1002/1521-3765(20020104)8:1<36::AID-CHEM36>3.0.CO;2-L>
• Eichelberger Uwe, Neundorf Ines, Hennig Lothar, Findeisen Matthias, Giesa Sabine, Müller Dietrich, Welzel Peter: Synthesis of analogues of the 2-O-alkyl glycerate part of the moenomycins. Tetrahedron 2002, 58, 545. <http://dx.doi.org/10.1016/S0040-4020(01)01167-X>
• Bennasar M.-Lluı̈sa, Zulaica Ester, Alonso Yolanda, Vidal Bernat, Vázquez Jesús T., Bosch Joan: Addition of chiral enolates to N-alkyl-3-acylpyridinium salts. Total synthesis of (+)-16-epivinoxine and (−)-vinoxine. Tet Asymm 2002, 13, 95. <http://dx.doi.org/10.1016/S0957-4166(02)00055-1>
• Kim Si-Min, Jun Jong-Gab: DIASTEREOSELECTIVE ALKYLATION AND ALDOL REACTIONS MEDIATED BY THE d-MANNITOL-DERIVED OXAZOLIDIN-2-ONE AS A CHIRAL AUXILIARY. Synth Common 2002, 32, 3851. <http://dx.doi.org/10.1081/SCC-120015404>
• Introduction of a New Chiral Oxazolidin-2-one Derived from D-Mannitol and Its Applications as a Chiral Auxiliary. Bulletin of the Korean Chemical Society 2002, 23, 749. <http://dx.doi.org/10.5012/bkcs.2002.23.5.749>
• Caddick S, Parr N.J, Pritchard M.C: Preparation of α-amino-carboxylic acid derivatives via diastereoselective reactions of glycine enolate equivalents. Tetrahedron 2001, 57, 6615. <http://dx.doi.org/10.1016/S0040-4020(01)00552-X>
• Hanessian Stephen, Moitessier Nicolas, Cantin Louis-David: Design and synthesis of MMP inhibitors using N-arylsulfonylaziridine hydroxamic acids as constrained scaffolds. Tetrahedron 2001, 57, 6885. <http://dx.doi.org/10.1016/S0040-4020(01)00641-X>
• Anaya de Parrodi Cecilia, Clara-Sosa Angel, Pérez Lydia, Quintero Leticia, Marañón Virginia, Toscano Rubén A., Aviña Judit A., Rojas-Lima Susana, Juaristi Eusebio: Highly diastereoselective alkylation, acylation and aldol condensation of cis- and trans-(N-acyloyl)hexahydrobenzoxazolidin-2-ones. Tet Asymm 2001, 12, 69. <http://dx.doi.org/10.1016/S0957-4166(00)00492-4>
• Chiu Pauline, Chen Bin, Cheng Kin Fai: A Rhodium Carbene Cyclization−Cycloaddition Cascade Strategy toward the Pseudolaric Acids. Org Lett 2001, 3, 1721. <http://dx.doi.org/10.1021/ol0159165>
• Jagt Richard B. C., Imbos Rosalinde, Naasz Robert, Minnaard Adriaan J., Feringa Ben L.: A catalytic route to acyclic chiral building blocks: Applications of the catalytic asymmetric conjugate addition of organozinc reagents to cyclic enones. Isr J Chem 2001, 41, 221. <http://dx.doi.org/10.1560/NHK0-C8JE-27G9-NUB3>
• Ter Wiel Matthijs K.J., Koumura Nagatoshi, Van Delden Richard A., Meetsma Auke, Harada Nobuyuki, Feringa Ben L.: Chiral overcrowded alkenes; Asymmetric synthesis of (3S,3′S)-(M,M)-(E)-(+)-1,1′,2,2′,3,3′,4,4′-octahydro-3,3′,7,7′-tetramethyl-4,4′-biphenanthrylidenes. Chirality 2000, 12, 734. <http://dx.doi.org/10.1002/1520-636X(2000)12:10<734::AID-CHIR6>3.0.CO;2-Q>
• Nicolaou K. C., Vourloumis Dionisios, Winssinger Nicolas, Baran Phil S.: Der Stand der Totalsynthese zu Beginn des 21. Jahrhunderts. Angew Chem 2000, 112, 46. <http://dx.doi.org/10.1002/(SICI)1521-3757(20000103)112:1<46::AID-ANGE46>3.0.CO;2-P>
• Mahrwald Rainer: Titanium(IV) Alkoxide Ligand Exchange with α-Hydroxy Acids:  The Enantioselective Aldol Addition. Org Lett 2000, 2, 4011. <http://dx.doi.org/10.1021/ol0002727>
• Fonquerna Sílvia, Rios Ramon, Moyano Albert, Pericàs Miquel A., Riera Antoni: Stereoselective Inter- and Intramolecular Pauson–Khand Reactions ofN-(2-Alkynoyl) Derivatives of Chiral Oxazolidin-2-ones. Eur J Org Chem 1999, 1999, 3459. <http://dx.doi.org/10.1002/(SICI)1099-0690(199912)1999:12<3459::AID-EJOC3459>3.0.CO;2-L>
• Tomooka Katsuhiko, Nagasawa Atsushi, Nakai Takeshi: Double Stereocontrol in .ALPHA.-Alkylation of Chiral Lithium Dienolates Generated from (E)-.ALPHA.,.BETA.-olefinic Amides and Esters. Chem Lett 1998, 1049. <http://dx.doi.org/10.1246/cl.1998.1049>
• Lützen Arne, Köll Peter: D-xylose derived oxazolidin-2-ones as chiral auxiliaries in stereoselective acylations and halogenations. Tet Asymm 1997, 8, 29. <http://dx.doi.org/10.1016/S0957-4166(96)00478-8>
• de Parrodi Cecilia Anaya, Juaristi Eusebio, Quintero Leticia, Clara-Sosa Angel: Preparation of enantiomerically pure cis- and trans-N-(propionyl)hexahydrobenzoxazolidin-2-ones. Tet Asymm 1997, 8, 1075. <http://dx.doi.org/10.1016/S0957-4166(97)00064-5>
• Lützen Arne, Köll Peter: d-Xylose derived oxazolidin-2-ones as chiral auxiliaries in stereoselective aldol reactions. Tet Asymm 1997, 8, 1193. <http://dx.doi.org/10.1016/S0957-4166(97)00096-7>
• Fonquerna Sílvia, Moyano Albert, Pericàs Miquel A., Riera Antoni: A convenient preparation of N-(2-alkynoyl) derivatives of chiral oxazolidin-2-ones and bornane-10,2-sultam. Tet Asymm 1997, 8, 1685. <http://dx.doi.org/10.1016/S0957-4166(97)00167-5>
• Tietze Lutz F., Schneider Christoph, Grote Andrea: Stereodivergent Hetero-Diels-Alder Reactions of Chiral 1-Oxa-1,3-butadienes through a Conformational Switch Induced by Lewis Acids. Chem Eur J 1996, 2, 139. <http://dx.doi.org/10.1002/chem.19960020205>
• Iseki Katsuhiko, Oishi Satoshi, Kobayashi Yoshiro: Reversal of stereoselectivity in the Evans aldol reaction of α,α-difluoro and α,α,α-trifluoro carbonyl compounds. Tetrahedron 1996, 52, 71. <http://dx.doi.org/10.1016/0040-4020(95)00858-6>
• Tyrrell Elizabeth, Tsang Michael W.H., Skinner George A, Fawcett John: The application of 1H nuclear magnetic resonance spectroscopy for the determination of the absolute configuration of chiral carboxylic acids. Tetrahedron 1996, 52, 9841. <http://dx.doi.org/10.1016/0040-4020(96)00516-9>
• Bauta William E., Booth John, Bos Mary E., DeLuca Mark, Diorazio Louis, Donohoe Timothy J., Frost Christopher, Magnus Nicholas, Magnus Philip, Mendoza José, Pye Philip, Tarrant James G., Thom Stephen, Ujjainwalla Feroze: Taxane diterpenes 1. Control of relative and absolute stereochemistry in intramolecular pyrylium ylide-alkene cyclizations for the synthesis of taxol precursors. Tetrahedron 1996, 52, 14081. <http://dx.doi.org/10.1016/0040-4020(96)00867-8>
• Miyake Tsutomu, Seki Masahiko, Nakamura Yoshinori, Ohmizu Hiroshi: Synthesis of a novel chiral 1, 3-benzoxazinone auxiliary and its application to highly diastereoselective aldol reaction. Tetrahetron Lett 1996, 37, 3129. <http://dx.doi.org/10.1016/0040-4039(96)00508-4>
• Köll Peter, Lützen Arne: D-xylose derived oxazolidin-2-ones as chiral auxiliaries in stereoselective alkylations. Tet Asymm 1996, 7, 637. <http://dx.doi.org/10.1016/0957-4166(96)00052-3>
• Tomooka Katsuhiko, Nagasawa Atsushi, Wei Shih-Yi, Nakai Takeshi: Chiral dienolate chemistry in remote asymmetric induction: the allylation / cope rearrangement sequence leading to γ-chiral α, β-unsaturated acid derivatives. Tetrahetron Lett 1996, 37, 8895. <http://dx.doi.org/10.1016/S0040-4039(96)02077-1>
• Kende Andrew S, Blass Benjamin E, Henry James R: Enantioselective total synthesis of didesepoxyrhizoxin. Tetrahetron Lett 1995, 36, 4741. <http://dx.doi.org/10.1016/0040-4039(95)00926-4>
• Makino Yukihiro, Iseki Katsuhiko, Fujii Kazuhisa, Oishi Satoshi, Hirano Tohru, Kobayashi Yoshiro: Reversal of π-face selectivity in the Evans aldol reaction with fluoral: A computational study on the transition states using semiempirical calculations. Tetrahetron Lett 1995, 36, 6527. <http://dx.doi.org/10.1016/0040-4039(95)01312-6>
• Köll Peter, Lützen Arne: Resolution of racemic carboxylic and sulfonic acids via D-xylose derived new cyclic carbamate reagents (oxazolidin-2-ones). Tet Asymm 1995, 6, 43. <http://dx.doi.org/10.1016/0957-4166(94)00347-E>
• Banks Malcolm R., Blake Alexander J., Brown Angus R., Cadogan J.I.G., Gaur Suneel, Gosney Ian, Hodgson Philip K.G., Thorburn Paul: Exploiting steric shielding: Tuning terpenoid-derived oxazolidin-2-ones as chiral auxiliaries for the Diels-Alder reaction. Tetrahetron Lett 1994, 35, 489. <http://dx.doi.org/10.1016/0040-4039(94)85088-7>
• Davies Stephen G., Evans Gary B., Mortlock Andrew A.: Bifunctional chiral auxiliaries 6: Alkylations of enolates derived from 1,3-diacylimidazolidine- 2-thiones and 1,3-diacylimidazolidin-2-ones. Tet Asymm 1994, 5, 585. <http://dx.doi.org/10.1016/0957-4166(94)80022-7>
• Mattson Anders, Boutelje John, Csöregh Ingeborg, Hjalmarsson Mats, Jacobsson Ulla, Lindbäck Mariane, Norin Torbjörn, Szmulik Peter, Hult Karl: Enhanced stereoselectivity in pig liver esterase catalysed diester hydrolysis. The role of a competitive nucleophile. biorg med chem 1994, 2, 501. <http://dx.doi.org/10.1016/0968-0896(94)80020-0>
• Davies Stephen G., Edwards Alison J., Evans Gary B., Mortlock Andrew A.: Bifunctional chiral auxiliaries 7: Aldol reactions of enolates derived from 1,3-diacyl-imidazolidine-2-thiones and 1,3-diacylimidazolidin-2-ones. Tetrahedron 1994, 50, 6621. <http://dx.doi.org/10.1016/S0040-4020(01)89691-5>
• Banks Malcolm R., Cadogan J.I.G., Gosney Ian, Gaur Suneel, Hodgson Philip K.G.: Highly regio- and stereo-specific preparation of a new carbohydrate-based 1,3-oxazin-2-one by the INIR method and its applications in some asymmetric transformations. Tet Asymm 1994, 5, 2447. <http://dx.doi.org/10.1016/S0957-4166(00)80392-4>
• Drewes Siegfried E., Malissar Dean G. S., Roos Gregory H. P.: Ephedrine-Derived Imidazolidin-2-ones. Broad Utility Chiral Auxiliaries in Asymmetric Synthesis. Chem Ber 1993, 126, 2663. <http://dx.doi.org/10.1002/cber.19931261216>
• Veit Andres, Lenz Roman, Seiler Martin E., Neuburger Markus, Zehnder Margareta, Giese Bernd: C2-Symmetrical Pyrrolidine Derivatives Chiral Auxiliaries in Radical Chemistry. HCA 1993, 76, 441. <http://dx.doi.org/10.1002/hlca.19930760128>
• Moreno-Mañas Marcial, Padros Imma: Preparation of oxazolidin-2-ones by oxidation of oxazolidine-2-thiones. A proton magnetic resonance structural study. J Heterocyclic Chem 1993, 30, 1235. <http://dx.doi.org/10.1002/jhet.5570300511>
• Braun Manfred, Sacha Hubert: Recent advances in Stereoselective Aldol Reactions of ester and thioester enolates. J Prakt Chem 1993, 335, 653. <http://dx.doi.org/10.1002/prac.19933350802>
• Davies Stephen G., Doisneau Gilles J.-M.: Base induced C-5 epimerisation of 4-methyl-5-phenyl oxazolidinones: Chiral auxiliaries derived from norephedrine and norpseudoephedrine. Tet Asymm 1993, 4, 2513. <http://dx.doi.org/10.1016/S0957-4166(00)82231-4>
• Sato Michito, Kahn Michael, Lin ZhaoLan, Johnson Michael E., Hayes Timothy K.: Design and synthesis of hypertrehalosemic hormoe mimetics. Biorg Med Chem Lett 1993, 3, 1277. <http://dx.doi.org/10.1016/S0960-894X(00)80331-5>
• Ager David J., East Michael B.: Methodology to establish 1,2- and 1,3-difunctionality for the synthesis of carbohydrate derivates. Tetrahedron 1992, 48, 2803. <http://dx.doi.org/10.1016/S0040-4020(01)90970-6>
• Ito Yoshio, Sasaki Akira, Tamoto Kastumi, Sunagawa Makoto, Terashima Shiro: Highly stereocontrolled synthesis of the 1β-methylcarbapenem key intermediate by the reformatsky reaction of 3-(2-bromopropionyl)-2-oxazolidone derivatives with a 4-acetoxy-2-azetidinone. Tetrahedron 1991, 47, 2801. <http://dx.doi.org/10.1016/S0040-4020(01)87086-1>
• Ito Yoshio, Terashima Shiro: Highly stereoselective reformatsky reactions of 3-(2-Bromopropionyl)-2-oxazolidone derivatives with various aldehydes. Tetrahedron 1991, 47, 2821. <http://dx.doi.org/10.1016/S0040-4020(01)87087-3>
• Lejeune J., Lallemand J.Y., Prangé T., Ricard L.: An Enantioselective Route Towards Clerodane Diterpenoids. Tetrahetron Lett 1991, 32, 2621. <http://dx.doi.org/10.1016/S0040-4039(00)78801-0>
• Young Gyu Kim, Konghyun Whang, Cooke R.J., Cha Jin K.: A stereoselective osmylation approach to polyoxygenated natural products. Synthesis of C(1)-C(7) and C(7)-C(13) subunits of erythronolide A. Tetrahetron Lett 1990, 31, 3275. <http://dx.doi.org/10.1016/S0040-4039(00)89042-5>
• Lamy-Schelkens Hélène, Ghosez Léon: Asymmetric Diels-Alder reactions of 1,3-disiloxycyclohexadiene with chiral acrylamides. Tetrahetron Lett 1989, 30, 5891. <http://dx.doi.org/10.1016/S0040-4039(01)93498-7>
• Pridgen Lendon N., Abdel-Magid A., Lantos I.: A predominately anti-stereoselective chiral metal directed aldol condensation with aromatic aldehydes. Tetrahetron Lett 1989, 30, 5539. <http://dx.doi.org/10.1016/S0040-4039(01)93794-3>
• Braun Manfred: Stereoselektive Aldolreaktionen mit α-unsubstituierten chiralen Enolaten. Angew Chem 1987, 99, 24. <http://dx.doi.org/10.1002/ange.19870990106>
• Hoffmann Reinhard W.: Stereoselektive Synthese von Bausteinen mit drei aufeinanderfolgenden stereogenen Zentren, wichtigen Vorstufen für polyketide Naturstoffe. Angew Chem 1987, 99, 503. <http://dx.doi.org/10.1002/ange.19870990604>
• Ito Yoshio, Terashima Shiro: A highly stereoselective synthesis of aldols employing the Reformatsky reaction of 3-(2-bromopropionyl)-2-oxazolidone derivatives with various aldehydes. Tetrahetron Lett 1987, 28, 6629. <http://dx.doi.org/10.1016/S0040-4039(00)96931-4>
• Nerz-Stonies Maryellen, Thornton Edward R.: Apparent chelation control in aldol reactions of chiral (Me2CHO)3Ti-enolates. Tetrahetron Lett 1986, 27, 897. <http://dx.doi.org/10.1016/S0040-4039(00)84131-3>
• Abdel-Magid Ahmed, Lantos Ivan, Pridgen Lendon N.: Aldol condensations of chiral α-haloimidates. A chiral darzens condensation procedure. Tetrahetron Lett 1984, 25, 3273. <http://dx.doi.org/10.1016/S0040-4039(01)81362-9>
• Kabalka George W.: Boron: boranes in organic synthesis annual survey covering the year 1981. J Organomet Chem 1983, 245, 1. <http://dx.doi.org/10.1016/S0022-328X(00)99420-8>
• Roush William R., Adam Michael A., Peseckis Steven M.: Regioselectivity of the reactions of trialkylaluminum reagents with 2,3-epoxyalcohols: Application to the synthesis of α-chiral aldehydes. Tetrahetron Lett 1983, 24, 1377. <http://dx.doi.org/10.1016/S0040-4039(00)81660-3>
• Drauz Karlheinz, Kleeman Axel, Martens Jürgen: Induction of Asymmetry by Amino Acids. Angew Chem Int Ed Engl 1982, 21, 584. <http://dx.doi.org/10.1002/anie.198205841>
• Seebach Dieter, Prelog Vladimir: The Unambiguous Specification of the Steric Course of Asymmetric Syntheses. Angew Chem Int Ed Engl 1982, 21, 654. <http://dx.doi.org/10.1002/anie.198206541>
• Hoffmann Reinhard W., Zeiß Hans-Joachim, Ladner Wolfgang, Tabche Susanne: Stereoselektive Synthese von Alkoholen, XI. Doppelte Stereodifferenzierung bei der Addition von Crotylboronsäureestern an Aldehyde:Prelog-Djerassi-Lacton. Chem Ber 1982, 115, 2357. <http://dx.doi.org/10.1002/cber.19821150628>
• Widler Leo, Seebaeh Dieter: Diastereoselektive Synthese von β-Methyl-homoallylalkoholen durchlk-Addition von (2-Butenyl)triphenoxytitan an Aldehyde. HCA 1982, 65, 1085. <http://dx.doi.org/10.1002/hlca.19820650340>
• Seebach Dieter, Beck Albert K., Mukhopadhyay Triptikumar, Thomas Elizabeth: Diastereoselective Synthesis of Nitroaldol Derivatives. HCA 1982, 65, 1101. <http://dx.doi.org/10.1002/hlca.19820650402>
• Narula Acharan S.: Stereoselective introduction of chiral centres in acylic precursors: a probe into the transition state for V5+-catalyzed t-butylhydroperoxide (TBHP) epoxidation of acyclic allylic alcohols and its synthetic implications. Tetrahetron Lett 1982, 23, 5579. <http://dx.doi.org/10.1016/S0040-4039(00)85899-2>