Alkyl structure-selectivity relationships E2 reactions of open-chain tosylates: Steric effects in the anti-pathway induced by dissociated and associated tert-butoxide base-Reference-Cited by-同舟云学术

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Alkyl structure-selectivity relationships E2 reactions of open-chain tosylates: Steric effects in the anti-pathway induced by dissociated and associated tert-butoxide base

Published:1977 Issue:12 Volume:42 Page:3421-3438
ISSN:0010-0765
Container-title:Collection of Czechoslovak Chemical Communications
language:en
Short-container-title:Collect. Czech. Chem. Commun.

Author:

Závada J.,Pánková M.

Publisher

Institute of Organic Chemistry & Biochemistry

Subject

General Chemistry

Cited by 11 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. Stereochemistry of 1,2-elimination reactions at the E2–E1cB interface—tert-butyl 3-tosyloxybutanoate and its thioester;Organic & Biomolecular Chemistry;2008

2. Preferential cis-olefin formation: A striking resemblance between alkali-alkoxide and alumina promoted eliminations in low polar solvents;Collection of Czechoslovak Chemical Communications;1990

3. Synthesis of triglycerides from 1,3-dibromopropan-2-ol;Journal of the Chemical Society, Perkin Transactions 2;1983

4. The effect of base concentration on orientation in E2 reactions: A common feature in metal alkoxide promoted olefin formation from alkyl halides and tosylates;Collection of Czechoslovak Chemical Communications;1981

5. Stereochemical and base species dichotomies in olefin-forming E2 eliminations;Chemical Reviews;1980-12-01

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