Direct and Electrophilic Preparation of α-Thiocyanatoketones and Aldehydes Using Thiocyanatotrimethylsilane and Sulfuryl Chloride

DOI: 10.1246/cl.1994.2275

Source and publish data:

Chemistry Letters p. 2275 - 2278 (1994)

Update date:2022-08-16

Topics:

Authors:

Tanabe, Yoo

Makita, Takuya

Mori, Kei

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Article abstract of DOI:10.1246/cl.1994.2275

The thiocyanato (-SCN) group was directly and regioselectively introduced into the α-position of ketones, aldehydes, and aldols in an electrophilic manner by the combined use of thiocyanatotrimethylsilane and sulfuryl chloride with or without cyclic sec-a

Full text of DOI:10.1246/cl.1994.2275

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