Asymmetric Synthesis of 5-Substituted γ-Lactones and Butenolides via Nucleophilic Additions to Oxycarbenium Ions Derived from 5(R)-(Menthyloxy)-4(R)- (phenylsulfanyl)-2(3H)-dihydrofuranone-Reference-Cited by-同舟云学术

Asymmetric Synthesis of 5-Substituted γ-Lactones and Butenolides via Nucleophilic Additions to Oxycarbenium Ions Derived from 5(R)-(Menthyloxy)-4(R)- (phenylsulfanyl)-2(3H)-dihydrofuranone

Published:1996-01-01 Issue:9 Volume:61 Page:2920-2921
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

van Oeveren Arjan¹,Feringa Ben L.¹

Affiliation:

1. Department of Organic and Molecular Inorganic Chemistry, Groningen Center for Catalysis and Synthesis, University of Groningen, Nijenborgh 4, 9747 AG Groningen, The Netherlands

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo960078r

Reference31 articles.

1. Easy Access to Optically Pure Functionalized γ-Alkylated Lactones starting from (2R, 3R)-Tartaric Acid

2. New Synthesis of All Four Isomers of 3-Hydroxy-4-methyl-.gamma.-butyrolactone by Stereoselective Intramolecular Lactonization. Application to Asymmetric Synthesis of Biologically Active Compounds

3. Enantioselective preparation of .beta.-alkyl-.gamma.-butyrolactones from functionalized ketene dithioacetals

4. Lipase-catalyzed kinetic resolution of methyl 4-hydroxy-5-tetradecynoate and its application to a facile synthesis of japanese beetle pheromone

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