C–C Bond Formation at α to a Trifluoromethyl Group. Cyanation and Allylation of α-TrifluoromethylatedN,O-Acetals-Reference-Cited by-同舟云学术

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C–C Bond Formation at α to a Trifluoromethyl Group. Cyanation and Allylation of α-TrifluoromethylatedN,O-Acetals

Published:1989-11 Issue:11 Volume:18 Page:1987-1988
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Fuchigami Toshio,Ichikawa Shinji,Konno Akinori

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/cl/18/11/18_11_1987/_pdf

Reference5 articles.

1. Electrolytic transformation of fluoroorganic compounds. 3. Highly regioselective anodic methoxylation of N-(2,2,2-trifluoroethyl)amines

2. 1,1-dihydroperfluoroalkylations of nucleophiles with (1,1-dihydroperfluoroalkyl)phenyliodonium triflates

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1. CF3-substituted carbocations: underexploited intermediates with great potential in modern synthetic chemistry;Beilstein Journal of Organic Chemistry;2021-02-03

2. 2.02 Allylsilanes, Allylstannanes, and Related Compounds;Comprehensive Organic Synthesis II;2014

3. A Catalytic Asymmetric Borono Variant of Hosomi-Sakurai Reactions with N,O-Aminals;Angewandte Chemie International Edition;2011-10-04

4. A Catalytic Asymmetric Borono Variant of Hosomi-Sakurai Reactions with N,O-Aminals;Angewandte Chemie;2011-10-04

5. Cyanotrimethylsilane;Encyclopedia of Reagents for Organic Synthesis;2011-09-15

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