Control of the Organocatalytic Enantioselective α-Alkylation of Vinylogous Carbonyl Enolates for the Synthesis of Tetrahydropyran Derivatives and Beyond-Reference-Cited by-同舟云学术

Control of the Organocatalytic Enantioselective α-Alkylation of Vinylogous Carbonyl Enolates for the Synthesis of Tetrahydropyran Derivatives and Beyond

Published:2021-05-28 Issue:12 Volume:23 Page:4688-4693
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Akula Pavan Sudheer¹,Wang Yung-Ju¹,Hong Bor-Cherng¹^ORCID,Lee Gene-Hsiang²,Chien Su-Ying²

Affiliation:

1. Department of Chemistry and Biochemistry, National Chung Cheng University, Chia-Yi, 621, Taiwan, R.O.C.

2. Instrumentation Center, National Taiwan University, Taipei, 106, Taiwan, R.O.C

Funder

Ministry of Science and Technology, Taiwan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c01426

Reference36 articles.

1. The Vinylogous Aldol Reaction: A Valuable, Yet Understated Carbon−Carbon Bond-Forming Maneuver

2. Recent Advances in Vinylogous Aldol Reactions and Their Applications in the Syntheses of Natural Products

3. The Vinylogous Aldol and Related Addition Reactions: Ten Years of Progress

4. Enolizable Alkylidene Heterocyclic and Carbocyclic Carbonyl Systems: Valuable Vinylogous Donor Substrates in Synthesis

5. New Developments of the Principle of Vinylogy as Applied to π-Extended Enolate-Type Donor Systems

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