An expeditious enantioselective synthesis of γ-lactones-Reference-Cited by-同舟云学术

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An expeditious enantioselective synthesis of γ-lactones

Published:1990-01 Issue:14 Volume:31 Page:1981-1984
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Michael Chong J.,Mar Eduardo K.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference18 articles.

1. Synthesis of the enantiomers of 4-substituted γ-lactones with known absolute configuration

2. A chelate‐controlled route to disubstituted and tetrasubstituted γ‐lactones stereoselectivity in lewis acid promoted additions to chiral methyl β‐formylcarboxylates

3. .alpha.-Alkoxyorganolithium reagents. A new class of configurationally stable carbanions for organic synthesis

4. Physical properties and synthetic utility of .alpha.-alkoxyorganolithium species as studied through ligand selectivity in tin-lithium exchange

5. The effects of in-sity trimethylsilyl chloride on the regioselectivity of the addition of α-alkoxy- and α-alkyl-substituted organocuprates to enals

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1. Lactone and Lactam Formation;Comprehensive Organic Transformations;2018-02-28

2. Conjugate Addition to α,β-Unsaturated Nitriles, Carboxylic Acids, and Derivatives;Comprehensive Organic Transformations;2018-02-28

3. 1.14 Oxygen-Stabilized Carbanions;Comprehensive Organic Synthesis II;2014

4. Organotin Chemistry;Organometallics in Synthesis;2013-06-26

5. Asymmetric Synthesis;Asymmetric Synthesis of Natural Products;2012-06-13

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