Nucleophilic Substitution of Vinylic Hydrogen Atoms by Carbanions | Zendy

Reetz Manfred T. | Zendy; Schinzer Dieter | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

Nucleophilic Substitution of Vinylic Hydrogen Atoms by Carbanions

Author(s) -

Reetz Manfred T.,

Schinzer Dieter

Publication year - 1977

Publication title -

angewandte chemie international edition in english

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 5.831

H-Index - 550

eISSN - 1521-3773

pISSN - 0570-0833

DOI - 10.1002/anie.197700442

Subject(s) - carbanion , elongation , chemistry , sequence (biology) , chain (unit) , nucleophilic substitution , nucleophile , hydrogen , substitution (logic) , terminal (telecommunication) , medicinal chemistry , stereochemistry , organic chemistry , catalysis , materials science , physics , computer science , metallurgy , ultimate tensile strength , programming language , telecommunications , biochemistry , astronomy

Chain elongation of activated terminal olefins can be accomplished by the reaction sequence (1) → (2) → (3). It is also feasible with R = tert ‐butyl, cyclopropyl, and other bulky groups.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research