Chelation-controlled nucleophilic additions. 2. A highly effective system for asymmetric induction in the reaction of organometallics with β-alkoxyaldehydes.-Reference-Cited by-同舟云学术

Chelation-controlled nucleophilic additions. 2. A highly effective system for asymmetric induction in the reaction of organometallics with β-alkoxyaldehydes.

Published:1980-01 Issue:11 Volume:21 Page:1035-1038
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Clark Still W.,Schneider Josef A.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference7 articles.

1. W. C. Still and J. H. McDonald, Tetrahedron Lett., preceding paper in this issue.

2. Stereochemistry of mannich bases—II

3. Stereochemistry of mannich bases-III

4. Organocopper chemistry. Halo-, cyano-, and carbonyl-substituted ketones from the corresponding acyl chlorides and organocopper reagents

5. PRODUCTION AND PROPERTIES OF 2,3-BUTANEDIOL: XXVII. CRYSTALLINE ESTERS SUITABLE FOR IDENTIFICATION AND ESTIMATION OF THE ISOMERIC 2,3-BUTANEDIOLS

Cited by 170 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. My 50-Plus Years of Academic Research Collaborations with Industry. A Retrospective;The Journal of Organic Chemistry;2024-06-12

2. Diastereoselective Transformation Using Group 2 and 13 Metal Salts;Comprehensive Chirality;2024

3. Carbonylchemie;Organische Synthesemethoden;2023

4. Evidence against Single-Electron Transfer in the Additions of Most Organomagnesium Reagents to Carbonyl Compounds;The Journal of Organic Chemistry;2020-05-14

5. Reactions of Allylmagnesium Reagents with Carbonyl Compounds and Compounds with C═N Double Bonds: Their Diastereoselectivities Generally Cannot Be Analyzed Using the Felkin–Anh and Chelation-Control Models;Chemical Reviews;2020-01-06