CrossRef enabled

PAC Archives

Archive →

Pure Appl. Chem., 1983, Vol. 55, No. 4, pp. 589-604

http://dx.doi.org/10.1351/pac198855040589

Stereo and regioselective openings of chiral 2,3-epoxy alcohols. Versatile routes to optically pure natural products and drugs. Unusual kinetic resolutions

K. B. Sharpless, C. H. Behrens, Tsutomu Katsuki, A. W. M. Lee, V. S. Martin, M. Takatani, S. M. Viti, F. J. Walker and S. S. Woodard

CrossRef Cited-by theme picture

CrossRef Cited-by Linking

  • Okazaki Hayato, Hanaya Kengo, Shoji Mitsuru, Hada Noriyasu, Sugai Takeshi: A new route toward 2-acetamido-4-O-methyl-2-deoxy-d-mannopyranose from a Ferrier derivative of tri-O-acetyl-d-glucal, which contributes to aldolase-catalyzed synthesis of laninamivir (CS-8958). Tetrahedron 2013, 69, 7931. <http://dx.doi.org/10.1016/j.tet.2013.07.018>
  • Stoyanova Malinka P., Shivachev Boris L., Nikolova Rosica P., Dimitrov Vladimir: Highly efficient synthesis of chiral aminoalcohols and aminodiols with camphane skeleton. Tetrahedron: Asymmetry 2013, 24, 1426. <http://dx.doi.org/10.1016/j.tetasy.2013.08.015>
  • Radha Krishna Palakodety, Prabhakar Sunchu, Sravanthi Chittela: The first stereoselective total synthesis of nicotlactone A. Tetrahedron Letters 2013, 54, 669. <http://dx.doi.org/10.1016/j.tetlet.2012.12.003>
  • Radha Krishna Palakodety, Nomula Rajesh, Venkata Ramana D.: First stereoselective total synthesis of decytospolides A and B. Tetrahedron Letters 2012, 53, 3612. <http://dx.doi.org/10.1016/j.tetlet.2012.05.011>
  • Radha Krishna Palakodety, Satyanarayana Mallula Venkata, Venkata Arun Kumar Pendyala: First stereoselective total synthesis of helicascolides A and C. Tetrahedron Letters 2012, 53, 4997. <http://dx.doi.org/10.1016/j.tetlet.2012.07.018>
  • Yadav J.S., Pandurangam T., Suman Kumar A., Adi Narayana Reddy P., Prasad A.R., Reddy B.V. Subba, Rajendraprasad K., Kunwar A.C.: The first stereoselective total synthesis of the Z-isomer of cytospolide E. Tetrahedron Letters 2012, 53, 6048. <http://dx.doi.org/10.1016/j.tetlet.2012.08.108>
  • Radha Krishna Palakodety, Ramana D. Venkata: Titanium(IV)-Promoted Regioselective Nucleophilic Ring-Opening Reaction of Chiral Epoxyallyl Alcohols with Acids as a Tool for Ready Access to Chiral 1,2,3-Triol Monoesters: Application to Stereoselective Total Synthesis of Macrolides. J Org Chern 2012, 77, 674. <http://dx.doi.org/10.1021/jo202199g>
  • Kahn Michael G. C., Weck Marcus: Highly crosslinked polycyclooctyl-salen cobalt (iii) for the hydrolytic kinetic resolution of terminal epoxides. Catal Sci Technol 2012, 2, 386. <http://dx.doi.org/10.1039/c1cy00290b>
  • Lin Hui, Liu Yan, Wu Zhong-Liu: Highly diastereo- and enantio-selective epoxidation of secondary allylic alcohols catalyzed by styrene monooxygenase. Chem Commun 2011, 47, 2610. <http://dx.doi.org/10.1039/c0cc04360e>
  • Alvarez Eleuterio, Díaz Maria Teresa, Zurita Dácil, Zárraga Miguel, Martín Julio D.: Model Studies Directed Towards Microalga Polyether Toxins. Bull Soc Chim Belges 2010, 99, 635. <http://dx.doi.org/10.1002/bscb.19900990904>
  • Kirschbaum Bettina, Stahl Ulrich, Volker Jäger: Synthesis of L-Erythro-α,β-Dihydroxy-GABA and γ-Hydroxy-L-Erythronine by Oxidative Degradation of Amino-4-Pentenediols. Bull Soc Chim Belges 2010, 103, 425. <http://dx.doi.org/10.1002/bscb.19941030716>
  • Welzel Peter: Anwendungen der Pummerer- Reaktion. Nachr Chem Tech Lab 2010, 31, 892. <http://dx.doi.org/10.1002/nadc.19830311108>
  • Der 2,3-Isopropylidenglycerinaldehyd-eine Modeverbindung?. Nachr Chem Tech Lab 2010, 32, 146. <http://dx.doi.org/10.1002/nadc.19840320211>
  • Mulzer Johann: Asymmetrische CC-Verknüpfungen über Epoxide. Nachr Chem Tech Lab 2010, 32, 310. <http://dx.doi.org/10.1002/nadc.19840320408>
  • Thijs Lambertus, Waanders Peter P., Stokkingreef Edwin H. M., Zwanenburg Binne: Synthesis of the optical antipodes of 4-alkyl-γ-lactones. Recl Trav Chim Pays-Bas 2010, 105, 332. <http://dx.doi.org/10.1002/recl.19861050917>
  • Legters Johan, Willems Johannes G. H., Thijs Lambertus, Zwanenburg Binne: Synthesis of functionalized amino acids by ring-opening reactions of aliphatically substituted aziridine-2-carboxylic esters. Recl Trav Chim Pays-Bas 2010, 111, 59. <http://dx.doi.org/10.1002/recl.19921110201>
  • Ogasawara Masamichi: Catalytic enantioselective synthesis of axially chiral allenes. Tet Asymm 2009, 20, 259. <http://dx.doi.org/10.1016/j.tetasy.2008.11.039>
  • Sureshkumar Devarajulu, Koutha Srinivasamurthy, Chandrasekaran Srinivasan: A New Selena-Aza-Payne-Type Rearrangement of Aziridinylmethyl Tosylates Mediated by Tetraselenotungstate. Eur J Org Chem 2007, 2007, 4543. <http://dx.doi.org/10.1002/ejoc.200700357>
  • Sagar Ram, Vijaya Raghava Reddy L., Saquib Mohammad, Kumar Brijesh, Shaw Arun K.: A consecutive approach towards the stereoselective synthesis of trisubstituted THF domains. Tet Asymm 2006, 17, 3294. <http://dx.doi.org/10.1016/j.tetasy.2006.12.010>
  • Stereospecific Synthesis of the (2R,3S)- and (2R,3R)-3-Amino-2-hydroxy-4-phenylbutanoic Acids from D-Glucono-δ-lactone. Bulletin of the Korean Chemical Society 2006, 27, 1211. <http://dx.doi.org/10.5012/bkcs.2006.27.8.1211>
  • Matsumoto Shoji, Ishii Michiko, Kimura Kazuto, Ogura Katsuyuki: Novel Synthesis of α-Amino Carboxamides and Their Related Compounds via α-Oxo Sulfones Starting from 2,2-Disulfonyloxiranes. Bull Chem Soc Jpn 2004, 77, 1897. <http://dx.doi.org/10.1246/bcsj.77.1897>
  • Kolodiazhnyi Oleg I.: Multiple stereoselectivity and its application in organic synthesis. Tetrahedron 2003, 59, 5953. <http://dx.doi.org/10.1016/S0040-4020(03)00911-6>
  • Fernandes Rodney A, Kumar Pradeep: Asymmetric dihydroxylation and one-pot epoxidation routes to (+)- and (−)-posticlure: a novel trans-epoxide as a sex pheromone component of Orgyia postica (Walker). Tetrahedron 2002, 58, 6685. <http://dx.doi.org/10.1016/S0040-4020(02)00685-3>
  • Dı́ez David, Beneitez M.Templo, Marcos Isidro S., Garrido N.M., Basabe P., Urones Julio G.: Regio- and stereoselective ring opening of epoxides. Enantioselective synthesis of 2,3,4-trisubstituted five-membered heterocycles. Tet Asymm 2002, 13, 639. <http://dx.doi.org/10.1016/S0957-4166(02)00160-X>
  • Vega-Pérez José M., Candela José I., Blanco Eugenia, Iglesias-Guerra Fernando: Stereoselective synthesis of epoxyalkyl glycoside precursors of glycosyl glycerol analogues from alkenyl glycosides of N-acetyl-d-glucosamine derivatives. Tet Asymm 2002, 13, 2471. <http://dx.doi.org/10.1016/S0957-4166(02)00649-3>
  • Mikami Koichi, Yoshida Akihiro: Regio- and enantioselective synthesis of allenic esters by samarium(II)-mediated reduction of propargylic compounds through dynamic kinetic protonation. Tetrahedron 2001, 57, 889. <http://dx.doi.org/10.1016/S0040-4020(00)01044-9>
  • Lee Woo-Wha, Shin Hyun Jung, Chang Sukbok: A rapid formal synthesis of the macrolide (−)-A26771B. Tet Asymm 2001, 12, 29. <http://dx.doi.org/10.1016/S0957-4166(01)00004-0>
  • Kitayama Takashi, Masuda Tomomi, Kawai Yasushi, Hill Richard K., Takatani Masahiro, Sawada Seiji, Okamoto Tadashi: The chemistry of zerumbone. Part 3: Stereospecific creation of five stereogenic centers by double Sharpless oxidation. Tet Asymm 2001, 12, 2805. <http://dx.doi.org/10.1016/S0957-4166(01)00505-5>
  • Vega-Pérez José M., Vega Margarita, Blanco Eugenia, Iglesias-Guerra Fernando: Stereoselective synthesis of oxiranes using oxazolidines derived from 2-amino-2-deoxy-d-allose as chiral auxiliaries. Tet Asymm 2001, 12, 3189. <http://dx.doi.org/10.1016/S0957-4166(01)00562-6>
  • Tronchet Jean M. J., Kovacs Imre, Seman Michel, Dilda Pierre, Clercq Erik De, Balzarini Jan: Highly Stereoselective Synthesis and Biological Properties of Nucleoside Analogues Bearing a Spiro Inserted Oxirane Ring. NUCLEOT NUCL 2000, 19, 775. <http://dx.doi.org/10.1080/15257770008035024>
  • Zhou Wei-Shan, Lu Zhi-Hui, Xu Yi-Ming, Liao Li-Xin, Wang Zhi-Min: Synthesis of optically active α-furfuryl amine derivatives and application to the asymmetric syntheses. Tetrahedron 1999, 55, 11959. <http://dx.doi.org/10.1016/S0040-4020(99)00669-9>
  • SEKI Masahiko, NAKAO Kazuya: Novel Synthesis of (-)-Bestatin from L-Aspartic Acid. Biosci Biotechnol Biochem 1999, 63, 1304. <http://dx.doi.org/10.1271/bbb.63.1304>
  • A. Ciufolini Marco, Xi Ning: Synthesis, chemistry and conformational properties of piperazic acids. Chem Soc Rev 1998, 27, 437. <http://dx.doi.org/10.1039/a827437z>
  • Cacciola Joseph, Alexander Richard S, Fevig John M, Stouten Pieter F.W: The synthesis of lysine α-ketoamide thrombin inhibitord via an epoxy amide ring opening. Tetrahetron Lett 1997, 38, 5741. <http://dx.doi.org/10.1016/S0040-4039(97)01205-7>
  • Haddad Nizar, Brik Ashraf, Grishko Michael: Studies towards total synthesis of borrelidin, regioselective methylation of bis-epoxides and structure determination. Tetrahetron Lett 1997, 38, 6079. <http://dx.doi.org/10.1016/S0040-4039(97)01372-5>
  • Dimitrov Vladimir, Philipova Irena, Simova Svetlana: Synthesis and absolute configuration of new chiral epoxyalcohols by stereoselective epoxidation of allylic and homoallylic alcohols with a (1R)-(+)-camphor skeleton. Tet Asymm 1996, 7, 1493. <http://dx.doi.org/10.1016/0957-4166(96)00168-1>
  • Amat Mercedes, Llor Núria, Hidalgo José, Bosch Joan, Molins Elies, Miravitlles Carles: New chiral non-racemic piperidine-derived epoxy lactams. Tet Asymm 1996, 7, 2501. <http://dx.doi.org/10.1016/0957-4166(96)00317-5>
  • Balavoine Gilbert G. A., Manoury Eric: Organometallic compounds in asymmetric synthesis: Oxygen atom transfer. Appl Organometal Chem 1995, 9, 199. <http://dx.doi.org/10.1002/aoc.590090305>
  • Denmark Scott E., Chen Chien-Tien: Enantioselective synthesis of alkylidene cyclohexanes by an asymmetric olefination/cross-coupling sequence. Heteroatom Chem 1995, 6, 133. <http://dx.doi.org/10.1002/hc.520060207>
  • Milner David J.: Selective manipulation of only one of two similar sites within a molecule ‘odin reactions’: Strategic advantage for synthesis and tactics available. J Chem Technol Biotechnol 1995, 63, 301. <http://dx.doi.org/10.1002/jctb.280630402>
  • Valpuesta Marí, Durante Patricia, López-Herrera Fidel J: Completely regioselective oxirane opening of (2S, 3R, 4R)-N,N-dimethyl-2,3-epoxy-4,5-O-osopropyliene-4,5-dihydroxypentanoamide by nitrogen nucleophiles. Tetrahetron Lett 1995, 36, 4681. <http://dx.doi.org/10.1016/0040-4039(95)00834-Y>
  • Pastó Mireia, Moyano Albert, Pericàs Miquel A., Riera Antoni: Enantioselective synthesis of fully protected anti 3-amino-2-hydroxy butyrates. Tet Asymm 1995, 6, 2329. <http://dx.doi.org/10.1016/0957-4166(95)00309-D>
  • Uenishi Jun'ichi, Motoyama Mitsuhiro, Nishiyama Yoshitaka, Hirota Yuichi, Kubo Yuki, Akashi Haruo: Intramolecular ring opening of a 2,3-epoxy alcohol by a xanthate anionic center; stereospecific preparation of 2-mercapto-1,3-diol units. Heteroatom Chem 1994, 5, 51. <http://dx.doi.org/10.1002/hc.520050110>
  • Savignac Monique, Durand Jean-Olivier, Genêt Jean-Pierre: A short synthesis of the unusual amino acid of cyclosporine (4R)-4-[(E)-2-butenyl]-4,N-dimethyl-L-threonine (MeBmt). Tet Asymm 1994, 5, 717. <http://dx.doi.org/10.1016/0957-4166(94)80034-0>
  • Duthaler Rudolf O.: Recent developments in the stereoselective synthesis of α-aminoacids. Tetrahedron 1994, 50, 1539. <http://dx.doi.org/10.1016/S0040-4020(01)80840-1>
  • Besse Pascale, Veschambre Henri: Chemical and biological synthesis of chiral epoxides. Tetrahedron 1994, 50, 8885. <http://dx.doi.org/10.1016/S0040-4020(01)85362-X>
  • Kotha Sambasivarao: Opportunities in asymmetric synthesis: An industrial prospect. Tetrahedron 1994, 50, 3639. <http://dx.doi.org/10.1016/S0040-4020(01)90388-6>
  • Wu Dauh-Rurng, Cramer Steven M., Belfort Georges: Kinetic resolution of racemic glycidyl butyrate using a multiphase membrane enzyme reactor: Experiments and model verification. Biotechnol Bioeng 1993, 41, 979. <http://dx.doi.org/10.1002/bit.260411009>
  • Santaniello Enzo, Ferraboschi Patrizia, Grisenti Paride: Lipase-catalyzed transesterification in organic solvents: Applications to the preparation of enantiomerically pure compounds. Enzyme Microbiology Technology 1993, 15, 367. <http://dx.doi.org/10.1016/0141-0229(93)90123-J>
  • Marson Charles M., Harper Steven, Walker Andrew J., Pickering Jane, Campbell Jonathan, Wrigglesworth Roger, Edge Simon J.: Lewis acid mediated reactions of 2,3-epoxyalcohols: an efficient stereocontrolled route to polycyclic diols. Tetrahedron 1993, 49, 10339. <http://dx.doi.org/10.1016/S0040-4020(01)80561-5>
  • Zhou Wei-Shan, Lu Zhi-Hui, Wang Zhi-Min: An efficient preparation of optically active α-furfuryl amide by kinetic resolution using the modified sharpless asymmetric epoxidation reagents. Tetrahedron 1993, 49, 2641. <http://dx.doi.org/10.1016/S0040-4020(01)86343-2>
  • Colvin Ernest W., König Wilfried A., Loreto Maria A., Rowden Janette Y., Tommasini Ivan: β-lactams from chirally-enriched (allenylmethyl)silanes. Biorg Med Chem Lett 1993, 3, 2405. <http://dx.doi.org/10.1016/S0960-894X(01)80965-3>
  • Banks Malcolm R., Blake Alexander J., Cadogan J.I.G., Dawson Ian M., Gosney Ian, Grant Keith J., Gaur Suneel, Hodgson Philip K.G., Knight Kevin S., Smith Glen W., Stevenson (nee Thomson) Dian E.: Enantiospecific preparation of [(2r,6s)-endo]-5-aza-1,10,10-trimethyl-3-oxatricyclo[5.2.1.02,6]decan-4-one by a nitrene-mediated route from [(1s)-endo]-(−)-borneol and its utility as a chiral auxiliary in some asymmetric transformations. Tetrahedron 1992, 48, 7979. <http://dx.doi.org/10.1016/S0040-4020(01)80472-5>
  • Atkinson Robert S., Kelly Brian J., Williams John: Amination with 3-acetoxyaminoquinazolin-4-(3h)ones: preparation of α-aminoacid esters by reaction with silyl ketene acetals followed by NN bond cleavage. Tetrahedron 1992, 48, 7713. <http://dx.doi.org/10.1016/S0040-4020(01)90382-5>
  • 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>
  • Clayden Jonathan, Collington Eric W., Warren Stuart: Asymmetric epoxidations and kinetic resolutions of δ-hydroxy allylic phosphine oxides. Tetrahetron Lett 1992, 33, 7043. <http://dx.doi.org/10.1016/S0040-4039(00)60928-0>
  • Norman Bryan H., Morris Michelle L.: A stereospecific synthesis of (−)-Bestatin from L-malic acid. Tetrahetron Lett 1992, 33, 6803. <http://dx.doi.org/10.1016/S0040-4039(00)61780-X>
  • Rayner Christopher M., Westwell Andrew D.: Lewis acid induced reaction of 2,3-epoxy phenylsulphoxides. Tetrahetron Lett 1992, 33, 2409. <http://dx.doi.org/10.1016/S0040-4039(00)74225-0>
  • Genêt Jean Pierre, Durand Jean Olivier, Savignac Monique, Pons Dominique: Asymmetric synthesis of MeBma analog of C9 amino acid present in cyclosporine. Tetrahetron Lett 1992, 33, 2497. <http://dx.doi.org/10.1016/S0040-4039(00)92224-X>
  • Zhou Wei-Shan, Lu Zhi-Hui, Wang Zhi-Min: An efficient preparation of optically active α-furfuryl amide by kinetic resolution using the modified sharpless asymmetric epoxidation reagent. Tetrahetron Lett 1991, 32, 1467. <http://dx.doi.org/10.1016/0040-4039(91)80360-I>
  • Canas Marc, Poch Marta, Verdaguer Xavier, Moyano Albert, Pericàs Miquel A., Riera Antoni: Regioselective ring opening of chiral epoxyalcohols by primary amines. Tetrahetron Lett 1991, 32, 6931. <http://dx.doi.org/10.1016/0040-4039(91)80447-E>
  • Jäger Volker, Schröter Detlef, Koppenhoefer Bernhard: Asymmetric sharpless epoxidation of divinylcarbinol. Erythro-D- and -L-4-pentenitols by hydrolysis of regioisomeric epoxy-4-pentenols. Tetrahedron 1991, 47, 2195. <http://dx.doi.org/10.1016/S0040-4020(01)96130-7>
  • Zhou Wei-Shan, Wei Dong: Preparation of optically active α-pyrryl carbinols by kinetic resolution using the modified Sharpless asymmetric epoxidation reagent. Tet Asymm 1991, 2, 767. <http://dx.doi.org/10.1016/S0957-4166(00)80455-3>
  • Jørgensen Karl Anker: A mechanistic approach to the asymmetric epoxidation of allylic alcohols and osmylation of alkenes. Tet Asymm 1991, 2, 515. <http://dx.doi.org/10.1016/S0957-4166(00)86105-4>
  • Levine S. G., Heard N. E.: Chemical Resolution of Allylic Alcohols. Synth Common 1991, 21, 549. <http://dx.doi.org/10.1080/00397919108016782>
  • Kumar Erno Mohacsi: Regioselective Epoxidation of Geranyl Palmitate with Metachloroperbenzoic Acid. Synth Common 1991, 21, 2257. <http://dx.doi.org/10.1080/00397919108055458>
  • Alvarez Eleuterio, Teresa Díaz M., Rodríguez Matías L., Martín. Julio D.: Tricyclic oxonium-directed addition: Regiochemistry and stereochemistry of the iodination reactions in 2,3-epoxy cyclooct-5-en-1-ols and 2,3-epoxy-5-en-1-one. Tetrahetron Lett 1990, 31, 1629. <http://dx.doi.org/10.1016/0040-4039(90)80035-K>
  • Ko Soo Y., Lee Albert W.M., Masamune Satoru, A. Reed Lawrence, Barry Sharpless K., Walker Frederick J.: Total synthesis of the L-hexoses. Tetrahedron 1990, 46, 245. <http://dx.doi.org/10.1016/S0040-4020(01)97596-9>
  • Pons Dominique, Savignac Monique, Genet Jean-Pierre: Efficient syntheses of enantiomerically pure L and D-allothreonines and (S) and (R) isoserines. Tetrahetron Lett 1990, 31, 5023. <http://dx.doi.org/10.1016/S0040-4039(00)97795-5>
  • Abraham W.-R., Stumpf B., Arfmann H.-A.: Chiral Intermediates by Microbial Epoxidations. Journal of Essential Oil Research 1990, 2, 251. <http://dx.doi.org/10.1080/10412905.1990.9697876>
  • Fráter Georg, Müller Urs: Synthesis of (+)-(4S, 8R)hyphen;8hyphen;Epi- and (−)-(4R, 8S)-4-Epi-β-bisabolol. HCA 1989, 72, 653. <http://dx.doi.org/10.1002/hlca.19890720405>
  • Komiotis Dimitri, Bessodes Michel, Antonakis Kostas: Synthesis of 1-[6,7-anhydro-4-O-tert-butyldimethylsilyl-2,3-O-isopropylidene-d(and -l)-threo-α-d-manno-octopyranosyl]thymines, precursors to higher-carbon sugar nucleosides. Carbohydrates Research 1989, 190, 153. <http://dx.doi.org/10.1016/0008-6215(89)84155-2>
  • Fiaud J.C., Legros J.Y.: Palladium-catalyzed asymmetric synthesis of axially chiral molecules. J Organomet Chem 1989, 370, 383. <http://dx.doi.org/10.1016/0022-328X(89)87300-0>
  • Mori Kenji: Synthesis of optically active pheromones. Tetrahedron 1989, 45, 3233. <http://dx.doi.org/10.1016/S0040-4020(01)81007-3>
  • Zárraga Miguel, Rodríguez Matias L, Ruiz-Pérez Catalina, Martín Julio D: Model studies directed toward microalga polyether macrolides: A route to 12-carbon tetrahydrofuran and tetrahydropyran subunits. Tetrahetron Lett 1989, 30, 3725. <http://dx.doi.org/10.1016/S0040-4039(01)80494-9>
  • Brunner Henri, Sicheneder Adolf: Synthese optisch aktiver Phosphane via Sharpless-Epoxidierung. Angew Chem 1988, 100, 730. <http://dx.doi.org/10.1002/ange.19881000526>
  • Brunner Henri, Sicheneder Adolf: Synthesis of Optically Active Phosphanes via Sharpless Epoxidation. Angew Chem Int Ed Engl 1988, 27, 718. <http://dx.doi.org/10.1002/anie.198807181>
  • Schmidt Richard R., Frische Klaus: De-novo-Synthese von Kohlenhydraten und verwandten Naturstoffen, 29. Synthese von partiell geschützten Zuckern ausmeso-Divinylglycol. Liebigs Ann Chem 1988, 1988, 209. <http://dx.doi.org/10.1002/jlac.198819880305>
  • Jarosz Sławomir: Epoxidation of higher sugar allylic alcohols. Carbohydrates Research 1988, 183, 217. <http://dx.doi.org/10.1016/0008-6215(88)84076-X>
  • Brown Herbert C., Rangaishenvi Milind V.: Organoboranes. J Organomet Chem 1988, 358, 15. <http://dx.doi.org/10.1016/0022-328X(88)87067-0>
  • Fiaud J.C., Legros J.Y.: Palladium-catalyzed asymmetric synthesis of axially dissymmetric 4-t-butyl-alkylidenecyclohexane derivative. Tetrahetron Lett 1988, 29, 2959. <http://dx.doi.org/10.1016/0040-4039(88)85057-3>
  • Satoh Tsuyoshi, Oohara Teruhiko, Yamakawa Koji: A novel approach to the synthesis of chiral epoxides and allylic alcohols by the use of optically active p-tolyl sulfinyl group as a chiral auxiliary. Tetrahetron Lett 1988, 29, 2851. <http://dx.doi.org/10.1016/0040-4039(88)85228-6>
  • Zaks Aleksey, Empie Mark, Gross Akiva: Potentially commercial enzymatic processes for the fine and specialty chemical industries. Trends in Biotechnol 1988, 6, 272. <http://dx.doi.org/10.1016/0167-7799(88)90123-0>
  • Sun Chong-Qing, Rich Daniel H.: Asymmetric synthesis of threo β-hydroxy-α-N-methyl amino acids and MeBMT analogs via epoxides1. (Part 1). Tetrahetron Lett 1988, 29, 5205. <http://dx.doi.org/10.1016/S0040-4039(00)80717-0>
  • Mulzer Johann, Angermann Alfred, Münch Winfried, Schlichthörl Günter, Hentzschel Angelo: Synthesis of (2R,3S)-1,2,3-Butanetriol Derivatives From (R)-2,3-O-Isopropylideneglyceraldehyde and of the (2S,3R)-Enantiomers FromD-Glucose. Application to the Synthesis of Enantiomerically Pure Muscarine. Liebigs Ann Chem 1987, 1987, 7. <http://dx.doi.org/10.1002/jlac.198719870103>
  • Schnurrenberger Peter, Hungerbühler Ernst, Seebach Dieter: Total Synthesis of (+)-Colletodiol from (S,S)-Tartrate and (R)-3-Hydroxybutanoate. Liebigs Ann Chem 1987, 1987, 733. <http://dx.doi.org/10.1002/jlac.198719870821>
  • Wang Zhi-Min, Zhou Wei-Shan: Asymmetric epoxidation of allylic alcohol by the modified sharpless reagent. Tetrahedron 1987, 43, 2935. <http://dx.doi.org/10.1016/S0040-4020(01)86832-0>
  • Miyashita Masaaki, Suzuki Toshio, Yoshikoshi Akira: Organoselenium-mediated reduction of α,β-epoxy ketones to β-hydroxy ketones: A new access to inter- and intramolecular aldols. Tetrahetron Lett 1987, 28, 4293. <http://dx.doi.org/10.1016/S0040-4039(00)96488-8>
  • Chong J.Michael, Cyr Douglas R., Mar Eduardo K.: Regioselective opening of 2,3-epoxy alcohols with organocuprates. Enhanced C-2 selectivity through solvent effects. Tetrahetron Lett 1987, 28, 5009. <http://dx.doi.org/10.1016/S0040-4039(00)96682-6>
  • Häfele Brigitte, Schröter Detlef, Jäger Volker: Synthese vonerythro-D- und -L-4-Pententriolen; selektive Epoxyallylalkohol-Hydrolyse unter Retention oder zweifacher Inversion (Enantiomerisierung). Angew Chem 1986, 98, 89. <http://dx.doi.org/10.1002/ange.19860980115>
  • Häfele Brigitte, Schröter Detlef, Jäger Volker: Synthesis oferythro-D- and -L-4-Pentenetriols. Selective Epoxy Allyl Alcohol Hydrolysis with Retention or Twofold Inversion (Enantiomerization). Angew Chem Int Ed Engl 1986, 25, 87. <http://dx.doi.org/10.1002/anie.198600871>
  • Mulzer Johann, Lammer Ortrud: Enantioselective diastereospecific synthesis ofanti-α-alkyl-β-hydroxy esters through cuprate opening of glycidic esters. Chem Ber 1986, 119, 2178. <http://dx.doi.org/10.1002/cber.19861190713>
  • Brimacombe John S., Hanna Roderick, Kabir Abul K.M.S.: Higher-carbon sugars: the synthesis of some decitols via the epoxide route. Carbohydrates Research 1986, 153, C7. <http://dx.doi.org/10.1016/S0008-6215(00)90278-7>
  • Brimacombe John S., Kabir Abul K.M.: Convenient syntheses of l-glycero-d-manno-heptose and d-glycero-d-manno-heptose. Carbohydrates Research 1986, 152, 329. <http://dx.doi.org/10.1016/S0008-6215(00)90316-1>
  • ApSimon J.W., Lee Collier T.: Recent advances in asymmetric synthesis-II. Tetrahedron 1986, 42, 5157. <http://dx.doi.org/10.1016/S0040-4020(01)82073-1>
  • Annunziata Rita, Cinquini Mauro, Cozzi Franco, Raimondi Laura, Stefanelli Stefania: Stereoselective synthesis of polyols precursors by allyl sulphinyl anion addition to chiral alkoxy aldehydes. Tetrahedron 1986, 42, 5451. <http://dx.doi.org/10.1016/S0040-4020(01)82096-2>
  • Mori Kenji, Ebata Takashi: Syntheses of optically active pheromones with an epoxy ring, (+)-disparlure and both the enantiomers of (3z,6z)--9,10-epoxy-3,6-heneicosadiene. Tetrahedron 1986, 42, 3471. <http://dx.doi.org/10.1016/S0040-4020(01)87314-2>
  • Hatakeyama Susumi, Sakurai Kuniya, Takano Seiichi: Enantio- and stereo-selective synthesis of 2,6-dideoxyhexoses from divinylcarbinol. Tetrahetron Lett 1986, 27, 4485. <http://dx.doi.org/10.1016/S0040-4039(00)84985-0>
  • Dai Li-xin, Lou Bo-liang, Zhang Ying-zhi, Guo Guang-zhong: Regioselective titanium mediated reductive opening of 2,3-epoxy alcohols. Tetrahetron Lett 1986, 27, 4343. <http://dx.doi.org/10.1016/S0040-4039(00)94270-9>
  • Masamune Satoru, Choy William, Petersen John S., Sita Lawrence R.: Doppelte Stereodifferenzierung und eine neue Strategie zur Stereokontrolle in der Organischen Synthese. Angew Chem 1985, 97, 1. <http://dx.doi.org/10.1002/ange.19850970104>
  • Masamune Satoru, Choy William, Petersen John S., Sita Lawrence R.: Double Asymmetric Synthesis and a New Strategy for Stereochemical Control in Organic Synthesis. Angew Chem Int Ed Engl 1985, 24, 1. <http://dx.doi.org/10.1002/anie.198500013>
  • Lee Albert W. M.: Mechanism of epimerization of 2,3-erythro-aldoses to 2,3-threo-Aldoses: An NMR study. Magn Reson Chem 1985, 23, 468. <http://dx.doi.org/10.1002/mrc.1260230612>
  • Mori Kenji, Otsuka Tatsuya: Synthesis of (2S,3S)-2,3-octanediol and (S)-2-hydroxy-3-octanone, the male sex pheromone of the grape borer xylotrechus pyrrhoderus. Tetrahedron 1985, 41, 553. <http://dx.doi.org/10.1016/S0040-4020(01)96499-3>
  • Thijs L., Stokkingreef E.H.M., Lemmens J.M., Zwanenburg B.: Enantio-controlled synthesis of the crocyclic C14-C23 subunit of cytochalasin b. Tetrahedron 1985, 41, 2949. <http://dx.doi.org/10.1016/S0040-4020(01)96622-0>
  • Chong J.Michael, Sharpless K.Barry: Regioselective openings of 2,3-epoxy acids with organocuprates. Tetrahetron Lett 1985, 26, 4683. <http://dx.doi.org/10.1016/S0040-4039(00)94923-2>
  • Saito Seiki, Bunya Norio, Inaba Masami, Moriwake Toshio, Torii Sigeru: A facile cleavage of oxirane with hydrazoic acid in dmf A new route to chiral β-hydroxy-α-amino acids. Tetrahetron Lett 1985, 26, 5309. <http://dx.doi.org/10.1016/S0040-4039(00)95024-X>
  • Garner Philip, Park Jung Min, Rotello Vincent: An enantioselective synthesis of the carzinophilin degradation product (2s,3s) 4-amino-2,3-dihydroxy-3-methylbutyric acid. Tetrahetron Lett 1985, 26, 3299. <http://dx.doi.org/10.1016/S0040-4039(00)98282-0>
  • Schweiter M.J., Sharpless K.Barry: The asymmetric epoxidation of -butyl substituted allylic alcohols. Tetrahetron Lett 1985, 26, 2543. <http://dx.doi.org/10.1016/S0040-4039(00)98832-4>
  • Nicolaou K.C., Duggan M.E., Ladduwahetty T.: Reactions of 2,3-epoxyhalides. Synthesis of optically active allylic alcohols and homoallylic epoxides. Tetrahetron Lett 1984, 25, 2069. <http://dx.doi.org/10.1016/S0040-4039(01)81163-1>
  • Kobayashi Susumu, Isobe Toshiyuki, Ohno Masaji: A stereocontrolled synthesis of (−)-bestatin from an acyclic allylamine by iodocyclocarbamation. Tetrahetron Lett 1984, 25, 5079. <http://dx.doi.org/10.1016/S0040-4039(01)91124-4>
  • Abushanab Elie, Bessodes Michel, Antonakis Kostas: Practical enantiospecific syntheses of (+) erythro-9- (2s-hydroxy-3r-nonyl) adenine. Tetrahetron Lett 1984, 25, 3841. <http://dx.doi.org/10.1016/S0040-4039(01)91182-7>
  • McGarvey Glenn J., Kimura Masayuki, Oh Taeboem, Williams J. Michael: Acyclic Stereoselective Synthesis of Carbohydrates. J Carbohydr Chem 1984, 3, 125. <http://dx.doi.org/10.1080/07328308408058813>
  • Narula Acharan S.: Stereoselective introduction of chiral centres in acyclic precursors : a probe into the transition state of m-chloroperbenzoic (m-CPBA) acid epoxidation of acyclic allylic alcohols and its synthetic implications. Tetrahetron Lett 1983, 24, 5421. <http://dx.doi.org/10.1016/S0040-4039(00)87885-5>
  • Oehlschlager Allan C., Czyzewska Eva: Chiral epoxides as precursors of chiral allenes. Tetrahetron Lett 1983, 24, 5587. <http://dx.doi.org/10.1016/S0040-4039(00)94148-0>