Competitive rate studies for some reactions involving the allyl, butenyl, αγ-dimethylallyl, and propyl Grignard reagents. the mechanism of the reactions of allylic Grignard reagents with electrophilic substrates.-Reference-Cited by-同舟云学术

Competitive rate studies for some reactions involving the allyl, butenyl, αγ-dimethylallyl, and propyl Grignard reagents. the mechanism of the reactions of allylic Grignard reagents with electrophilic substrates.

Published:1970-01 Issue:13 Volume:11 Page:1045-1048
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Felkin Hugh,Frajerman Claude

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference15 articles.

1. Allylic Rearrangements. XVI. The Addition of the Butenyl Grignard Reagent to Some Simple Carbonyl Compounds1

2. The stereochemical course of epoxide ring opening by allylic grignard reagents

Cited by 38 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. Conformationally Biased Ketones React Diastereoselectively with Allylmagnesium Halides;The Journal of Organic Chemistry;2022-02-15

2. Addition of Chloroprene Grignards to Aromatic Aldehydes: Synthesis of Homoallenyl Alcohols;Organic Letters;2021-03-17

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

4. 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

5. Mechanistic Insight into Additions of Allylic Grignard Reagents to Carbonyl Compounds;The Journal of Organic Chemistry;2018-08-06