CONVENIENT SYNTHESES OF ALKYL THIOCYANATES AND ALKYL SELENOCYANATES FROM STERICALLY HINDERED OLEFIN VIA HYDROBORATION. SELECTIVE REACTIONS OF SECONDARY OR TERTIARY ALKYL GROUP IN MIXED TRIALKYLBORANES WITH FERRIC THIOCYANATE OR FERRIC SELENOCYANATE-Reference-Cited by-同舟云学术

CONVENIENT SYNTHESES OF ALKYL THIOCYANATES AND ALKYL SELENOCYANATES FROM STERICALLY HINDERED OLEFIN VIA HYDROBORATION. SELECTIVE REACTIONS OF SECONDARY OR TERTIARY ALKYL GROUP IN MIXED TRIALKYLBORANES WITH FERRIC THIOCYANATE OR FERRIC SELENOCYANATE

Published:1976-10-05 Issue:10 Volume:5 Page:1115-1118
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Arase Akira,Masuda Yuzuru

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference4 articles.

1. Reactions of Organoboranes with Ferric Chloride and Thiocyanate. Convenient Syntheses of Alkyl Chlorides and Thiocyanates from OlefinsviaHydroboration

2. Carbonylation of thexyldialkylboranes. New general synthesis of ketones

3. Carbonylation of the organoboranes from the cyclic hydroboration of dienes with thexylborane. Simple procedure for the conversion of dienes into cyclic ketones

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