Chiral dienolate chemistry in remote asymmetric induction: The asymmetric aldol / oxycope strategy for asymmetric synthesis of γ,δ-dichiral α, β-unsaturated acid derivatives-Reference-Cited by-同舟云学术

Chiral dienolate chemistry in remote asymmetric induction: The asymmetric aldol / oxycope strategy for asymmetric synthesis of γ,δ-dichiral α, β-unsaturated acid derivatives

Published:1996-12 Issue:49 Volume:37 Page:8899-8900
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Tomooka Katsuhiko,Nagasawa Atsushi,Wei Shih-Yi,Nakai Takeshi

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference8 articles.

1. Tomooka K.; Nagasawa A.; Wei S.-Y.; Nakai T., the preceding paper

2. This work was presented at the International Chemical Congress of Pacific Basin Societies,1995

3. Silyloxy-cope rearrangement of chiral aldol adducts

4. Bornane sultam-directed asymmetric synthesis of crystalline, enantiomerically pure syn aldols

5. The geometric and diastereomeric purity were determined by HPLC (ODS, CH3CN/H2O) and 1H NMR analysis (cf. ref7)

Cited by 39 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Copper-Catalyzed Reductive Ireland–Claisen Rearrangements of Propargylic Acrylates and Allylic Allenoates;The Journal of Organic Chemistry;2021-12-17

2. Dramatic Effect of γ-Heteroatom Dienolate Substituents on Counterion Assisted Asymmetric Anionic Amino-Cope Reaction Cascades;Journal of the American Chemical Society;2021-04-12

3. Enantio- and diastereoselective synthesis of syn -β-hydroxy-α-alkenyl carboxamides via reductive aldol reactions of morpholine 4-methyl-2,3-pentadienoic carboxamide with diisopinocampheylborane;Tetrahedron Letters;2015-06

4. Rearrangements Reactions;Key Chiral Auxiliary Applications;2014

5. Addition To C=O Bonds III;Key Chiral Auxiliary Applications;2014