Pure and Applied Chemistry

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• Shi Junxing, Linden Anthony, Heimgartner Heinz: Reactions of Acid Chlorides/Ketenes with 2-Substituted 4,5-Dihydro-4,4-dimethyl-1,3-thiazoles: Formation of Penam Derivatives. HCA 2013, 96, 1462. <http://dx.doi.org/10.1002/hlca.201300165>
• Shaikh Aarif L., Esparza Orlando, Banik Bimal K.: An Efficient Synthesis of Optically Active trans-(3R,4R)-3-Acetoxy-4-aryl-1-(chrysen-6-yl)azetidin-2-ones Using (+)-Car-3-ene as a Chiral Auxiliary. J Helv Chim Acta 2011, 94, 2188. <http://dx.doi.org/10.1002/hlca.201100225>
• Schilling Christine I., Jung Nicole, Biskup Moritz, Schepers Ute, Bräse Stefan: Bioconjugation via azide–Staudinger ligation: an overview. Chem Soc Rev 2011, 40, 4840. <http://dx.doi.org/10.1039/c0cs00123f>
• Thompson Sam, Coyne Anthony G., Knipe Peter C., Smith Martin D.: Asymmetric electrocyclic reactions. Chem Soc Rev 2011, 40, 4217. <http://dx.doi.org/10.1039/c1cs15022g>
• Palomo Claudio, Cossío Fernando P., Cuevas Carmen, Ontoria Jesús M., Odriozola José M., Munt Simon: Synthetic Aspects of Homochiral β-Lactams Derived from N-Protected α-Aminoimines Via Asymmetric [2+2] Cycloaddition Reaction. Bull Soc Chim Belges 2010, 101, 541. <http://dx.doi.org/10.1002/bscb.19921010703>
• Tang Ke, Wang Jinhu, Cheng Xueli, Hou Qianqian, Liu Yongjun: Theoretical Investigations towards the Staudinger Reaction Catalyzed by N-Heterocyclic Carbene: Mechanism and Stereoselectivity. Eur J Org Chem 2010, 2010, 6249. <http://dx.doi.org/10.1002/ejoc.201000774>
• Li Gong-Qiang, Li Yi, Dai Li-Xin, You Shu-Li: Enantioselective Synthesis of cis-4-Formyl-β-lactams via Chiral N-Heterocyclic Carbene-Catalyzed Kinetic Resolution. Adv Synth Catal 2008, 350, 1258. <http://dx.doi.org/10.1002/adsc.200800071>
• Shaikh A.L., Kale A.S., Shaikh Md. Abrar, Puranik Vedavati G., Deshmukh A.R.A.S.: Asymmetric synthesis of β-lactams by [2+2] cycloaddition using 1,4:3,6-dianhydro-d-glucitol (isosorbide) derived chiral pools. Tetrahedron 2007, 63, 3380. <http://dx.doi.org/10.1016/j.tet.2007.02.022>
• Bernardi Luca, Bonini Bianca F., Comes-Franchini Mauro, Dessole Gabriella, Fochi Mariafrancesca, Ricci Alfredo: One-Pot Synthesis of Novel Enantiomerically Pure and Racemic 4-Ferrocenyl-β-lactams and Their Reactivity in Acidic Media. Eur J Org Chem 2005, 2005, 3326. <http://dx.doi.org/10.1002/ejoc.200500170>
• Arun M, Joshi S.N, Puranik V.G, Bhawal B.M, Deshmukh A.R.A.S: Asymmetric synthesis of azetidin-2-ones by [2+2] cycloaddition using chiral imines derived from d-(+)-glucose. Tetrahedron 2003, 59, 2309. <http://dx.doi.org/10.1016/S0040-4020(03)00239-4>
• Basak Amit, Ghosh Subhash Chandra, Bhowmich Tandra, Das Amit K, Bertolasi Valerio: An asymmetric synthesis of β-lactams: on the use of chiral oxazolidones in the Kinugasa reaction. Tetrahetron Lett 2002, 43, 5499. <http://dx.doi.org/10.1016/S0040-4039(02)00974-7>
• Filomena Costa M, da Costa M.Rute G, Marcelo Curto M.J, Magrinho M, Damas Ana M, Gales Luis: Synthesis of chiral (7R)-[η6-5-(N,N-dimethylamino)-7-formyl-1,3-benzodioxole]chromium complex and its application in the synthesis of optically active cis-β-lactams. J Organomet Chem 2001, 632, 27. <http://dx.doi.org/10.1016/S0022-328X(01)00806-3>
• Lee Jong-Cheol, Kim Geun Tae, Shim Young Key, Kang Sung Ho: An asymmetric aminohydroxylation approach to the stereoselective synthesis of cis-substituted azetidinone of loracarbef. Tetrahetron Lett 2001, 42, 4519. <http://dx.doi.org/10.1016/S0040-4039(01)00757-2>
• Hassan Hammed H. A. M., Soliman Raafat: Synthesis and GC-Eims Analyses of Optically Pure 3-Hydroxy-2-Azetidinones Having N-Sulfonamide Drugs Side Chain. Synth Common 2000, 30, 2465. <http://dx.doi.org/10.1080/00397910008087410>
• Palomo Claudio, Aizpurua Jesus M., Ganboa Iñaki, Oiarbide Mikel: Asymmetric Synthesis of β-Lactams by Staudinger Ketene-Imine Cycloaddition Reaction. Eur J Org Chem 1999, 1999, 3223. <http://dx.doi.org/10.1002/(SICI)1099-0690(199912)1999:12<3223::AID-EJOC3223>3.0.CO;2-1>
• Palomo Claudio, Aizpurua Jesus Maria: Asymmetric synthesis of 3-amino-β-lactamsvia Staudinger ketene-imine cycloaddition reaction (review). Chem Heterocycl Compd 1998, 34, 1222. <http://dx.doi.org/10.1007/BF02256803>
• Barreau Michel, Commerçon Alain, Mignani Serge, Mouysset Dominique, Perfetti Patricia, Stella Lucien: Stereoselective synthesis of racemic α-amino-acid derivatives with a β-lactam skeleton: Application of the Staudinger reaction to chiral imines of methyl glyoxylate. Tetrahedron 1998, 54, 11501. <http://dx.doi.org/10.1016/S0040-4020(98)00683-8>
• Palomo Claudio, Aizpurua Jesus M., Legido Marta, Mielgo Antonia, Galarza Regina: A Contribution to the Asymmetric Synthesis of 3-Amino β-Lactams: The Diastereoselective [2+2] Cycloaddition Reaction of Chiral Aminoketene Equivalents with Enolizable Aldehyde-Derived Imines. Chem Eur J 1997, 3, 1432. <http://dx.doi.org/10.1002/chem.19970030909>
• Gunda Tamas E, Sztaricskai Ferenc: 2-Amino-1-phenyl-propan-1,3-diol as chiral auxiliary. Application in the synthesis of cis 3-Phthalimido-4-styryl-2-azetidinones. Tetrahedron 1997, 53, 7985. <http://dx.doi.org/10.1016/S0040-4020(97)00483-3>
• de Queiroz A.A.A., Barrak ��.R., de Castro S.C., Barcza Marcos V., de M. Carneiro Jose W., Serra Antonio A., Barboza Jayne C.S., Costa Maria Cristina Andreazza, Gaudio Anderson Coser, Takahata Yuji: Thermodynamic analysis of the surface of biomaterials. Journal of Molecular Structure: THEOCHEM 1997, 394, 271. <http://dx.doi.org/10.1016/S0166-1280(96)04844-0>
• Jayaraman M., Srirajan V., Deshmukh A.R.A.S., Bhawal B.M.: Modulating steric effects in diastereoselective Staudinger reaction: Synthesis of optically pure cis-β-lactams. Tetrahedron 1996, 52, 3741. <http://dx.doi.org/10.1016/0040-4020(96)00048-8>
• Srirajan V., Puranik Vedavati G., Deshmukh A.R.A.S., Bhawal Baburao M.: An efficient use of Oppolzer sultam for Diastereospecific Synthesis of cis-β-Lactams. Tetrahedron 1996, 52, 5579. <http://dx.doi.org/10.1016/0040-4020(96)00193-7>
• Srirajan V., Deshmukh A.R.A.S., Bhawal B.M.: An efficient synthesis of cis-3-hydroxy-4-phenyl-β-lactams: Precursor for taxol side chain. Tetrahedron 1996, 52, 5585. <http://dx.doi.org/10.1016/0040-4020(96)00200-1>
• Bandini Elisa, Martelli Giorgio, Spunta Giuseppe, Bongini Alessandro, Panunzio Mauro: Trans -Diastereoselective synthesis of 3-phthalimido β-lactams via a two step-staudinger reaction. Tetrahetron Lett 1996, 37, 4409. <http://dx.doi.org/10.1016/0040-4039(96)00841-6>
• Vassilev Vassil P., Uchiyama Taketo, Kajimoto Tetsuya, Wong Chi-Huey: An efficient chemo-enzymatic synthesis of α-amino-β-hydroxy-γ-butyrolactone. Tetrahetron Lett 1995, 36, 5063. <http://dx.doi.org/10.1016/0040-4039(95)00924-2>
• Asao Naoki, Uyehara Tadao, Tsukada Naofumi, Yamamoto Yoshinori: Asymmetric Synthesis of a .BETA.-Lactan Framework via the Conjugate Addition of Amidocuprates(I) to Chiral Enoates. Bull Chem Soc Jpn 1995, 68, 2103. <http://dx.doi.org/10.1246/bcsj.68.2103>
• Arrastia Iosune, Arrieta Ana, Ugalde Jesus M., Cossío Fernando P., Lecea Begoña: Theoretical and experimental studies on the periselectivity of the cycloaddition reaction between activated ketenes and conjugated imines. Tetrahetron Lett 1994, 35, 7825. <http://dx.doi.org/10.1016/0040-4039(94)80128-2>
• L. van Maanen Hendrik, T.B.H. Jastrzebski Johann, Kooijman Huub, L. Spek Anthony, van Koten Gerard: Highly functionalized β-enamino esters via C-C coupling reactions of lithium enolates of protected glycine esters and isothiocyanates. Tetrahedron 1994, 50, 11509. <http://dx.doi.org/10.1016/S0040-4020(01)89288-7>
• Arrieta Ana, Ugalde Jesus M., Cossío Fernando P., Lecea Begoña: Role of the isomerization pathways in the Staudinger reaction. A theoretical study on the interaction between activated ketenes and imidates. Tetrahetron Lett 1994, 35, 4465. <http://dx.doi.org/10.1016/S0040-4039(00)73385-5>
• Asao Naoki, Shimada Takashi, Tsukada Naofumi, Yamamoto Yoshinori: Highly stereocontrolled and concise asymmetric synthesis of the β-Lactam framework via a TCC method. Tetrahetron Lett 1994, 35, 8425. <http://dx.doi.org/10.1016/S0040-4039(00)74424-8>
• Baldoli Clara, Del Buttero Paola, Licandro Emanuela, Maiorana Stefano, Papagni Antonio: Tricarbonyl(η6arene)chromium(0) complexes as chiral auxiliaries. Homochiralβ-lactams synthesis “via” [2+2] cycloaddition reaction. Tet Asymm 1994, 5, 809. <http://dx.doi.org/10.1016/S0957-4166(00)86233-3>
• Bourzat Jean Dominique, Commerçon Alain: A practical access to chiral phenylisoserinates, preparation of Taxotere® analogs. Tetrahetron Lett 1993, 34, 6049. <http://dx.doi.org/10.1016/S0040-4039(00)61724-0>
• Kennington John W., Li Wei, Deshong Philip: Synthesis of Δ⁴-isoxazolines at high pressures. A new approach to the preparation of β-lactam derivatives?. High Pressure Science and Technology 1993, 11, 163. <http://dx.doi.org/10.1080/08957959208201702>
• Duczek Wolfram, Jähnisch Klaus, Kunath Annamarie, Reck Günter, Winter Gabriele, Schulz Burkhard: Zur Chemie der Mucohalogensäuren, VII. Asymmetrische Synthese von β-Lactam-Derivaten durch Keten — Imin-Cycloaddition unter Verwendung chiraler Mucochlorsäure-Derivate. Liebigs Ann Chem 1992, 1992, 781. <http://dx.doi.org/10.1002/jlac.1992199201129>
• Georg Gunda I., Akgün Eyüp, Mashava Peter M., Milstead Mark, Ping He, Wu Zhi-jun, Velde David Vander, Takusagawa Fusao: Galactose-Imines in the staudinger reaction. Tetrahetron Lett 1992, 33, 2111. <http://dx.doi.org/10.1016/0040-4039(92)88153-V>
• Kobayashi Yuko, Takemoto Yoshiji, Kamijo Tetsuhide, Harada Hiromu, Ito Yoshio, Terashima Shiro: A stereoselective synthesis of the (2R, 3S)- and (2S, 3R)-3-amino-2-hydroxybutyric acid derivatives, the key components of a renin inhibitor and bestatin. Tetrahedron 1992, 48, 1853. <http://dx.doi.org/10.1016/S0040-4020(01)88510-0>
• Palomo Claudio, Aizpurua Jesus M., Ontoria Jesus M., Iturburu Miren: A concise stereoselective approach to β-Alkylaspartates from β-Lactams via [2 + 2] cycloaddition reaction of ketenes to glyoxylic ester-derived imines. Tetrahetron Lett 1992, 33, 4823. <http://dx.doi.org/10.1016/S0040-4039(00)61295-9>
• Frazier Jeffery W., Staszak Mike A., Weigel Leland.O.: Enantioselective synthesis of loracarbef from sodium erythorbate. Tetrahetron Lett 1992, 33, 857. <http://dx.doi.org/10.1016/S0040-4039(00)91559-4>
• Palomo Claudio, Cossío Fernando P., Ontoria Jesús M., Odriozola José M.: Preparation of chiral 3-unsubstituted β-lactams from 3-hydroxy β-lactams by using the alkoxyketene-imine cycloaddition reaction as an approach to the azetidinone ring: A formal synthesis of the carbapenem antibiotic (+)-PS-5. Tetrahetron Lett 1991, 32, 3105. <http://dx.doi.org/10.1016/0040-4039(91)80701-7>
• Palomo Claudio, Cossío Fernando P., Cuevas Carmen: Asymmetric synthesis of monocyclic β-lactams: application of imines derived from chiral N-protected α-amino aldehydes in the staudinger reaction. Tetrahetron Lett 1991, 32, 3109. <http://dx.doi.org/10.1016/0040-4039(91)80702-8>
• van der Steen Fred H., van Koten Gerard: Syntheses of 3-amino-2-azetidinones: A literature survey. Tetrahedron 1991, 47, 7503. <http://dx.doi.org/10.1016/S0040-4020(01)88276-4>
• Georg Gunda I., Mashava Peter M., Guan Xiangming: An improved method for the stereoselective synthesis of β-lactams from carboxylic acids and imines. Tetrahetron Lett 1991, 32, 581. <http://dx.doi.org/10.1016/S0040-4039(00)74832-5>
• Georg Gunda I., Mashava Peter M., Akgün Eyüp, Milstead Mark W.: Asymmetric synthesis of β-lactams and n-benzoyl-3-phenylisoserines via the staudinger reaction. Tetrahetron Lett 1991, 32, 3151. <http://dx.doi.org/10.1016/S0040-4039(00)79708-5>
• Gunda Tamas E, Vieth Siegfried, Kövér Katalin E, Sztaricskai Ferenc: Enantiospecific synthesis and absolute configuration of β-lactam, intermediates from 2-amino-1-phenyl-1,3-propanediols. Tetrahetron Lett 1990, 31, 6707. <http://dx.doi.org/10.1016/S0040-4039(00)97153-3>
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