anti-Selective aldol reactions of chiral alcohol substituted γ-benzyloxyl vinylogous urethanes and the synthesis of 3-benzyloxyl-4-hydroxylalkan-2-ones-Reference-Cited by-同舟云学术

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anti-Selective aldol reactions of chiral alcohol substituted γ-benzyloxyl vinylogous urethanes and the synthesis of 3-benzyloxyl-4-hydroxylalkan-2-ones

Published:2017-11 Issue:11 Volume:28 Page:1573-1581
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Li Yu-Jang,Chung Chuan-Chung,Chen Pin-Zu

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference24 articles.

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

2. A new protocol for the diastereoselective formation of lactones from either achiral or chiral vinylogous urethanes

3. Nonracemic Syn-Selective Aldol Reactions with a Second-Generation Vinylogous Urethane Lithium Enolate

4. Total Synthesis of (−)-Virginiamycin M2 Using Second-Generation Vinylogous Urethane Chemistry

5. An enantioselective solutions towards synthesizing “skip” 1,3 dimethyl stereocenters. A synthesis of 4S(2E,4R∗,6R∗)-4,6-Dimethyl-2-octenoic acid

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1. Concise Synthesis of (-)-isoaltholactone and (±)-5- epi -OBn-Goniotriol;Synthetic Communications;2024-05-19

2. Synthetic Approaches to α‐, β‐, γ‐, and δ‐Lycoranes;European Journal of Organic Chemistry;2023-08-11

3. Six-Membered Ring Systems: With O and/or S Atoms;Progress in Heterocyclic Chemistry;2018

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