Rearrangement of epoxides in non-aldol aldol process: Allylic vs. Tertiary and secondary carbocationic centers-Reference-Cited by-同舟云学术

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Rearrangement of epoxides in non-aldol aldol process: Allylic vs. Tertiary and secondary carbocationic centers

Published:1999-04 Issue:16 Volume:40 Page:3129-3132
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Jung Michael E.,Marquez Rodolfo

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference32 articles.

1. Enantiospecific synthesis of all four diastereomers of 2-methyl-3-[(trialkylsilyl)oxy]alkanals: facile preparation of aldols by non-aldol chemistry

2. For an extension of this method to bis(propionates), see: Jung, M. E.; Lee, W. S., submitted for publication.

3. Recent developments in asymmetric aldol methodology

4. The Aldol Addition Reaction;Heathcock,1984

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1. Epoxide-Based Synthetic Approaches toward Polypropionates and Related Bioactive Natural Products;International Journal of Molecular Sciences;2023-03-24

2. Preparation of β-hydroxyketones (aldols) from the alkylation of O-silyl aryl cyanohydrins with epoxides;Tetrahedron Letters;2023-02

3. Synthetic Studies on the Viridin Skeleton through Regio- and Stereoselective Functionalization of the AE-Ring Moiety;Synlett;2021-06-11

4. Borinic Acid/Halide Co-catalyzed Semipinacol Rearrangements of 2,3-Epoxy Alcohols;Organic Letters;2018-08-15

5. Total Synthesis of ent-Ascospiroketal B;The Journal of Organic Chemistry;2018-02-08

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