Premium
Displacement of the indolyl sulfide linkage in the synthesis of 3‐substituted indoles
Author(s) -
Bennett Richard,
Maggiolo Allison,
Shah Tushar
Publication year - 1981
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570180232
Subject(s) - chemistry , sulfide , alkoxy group , decomposition , single displacement reaction , displacement (psychology) , methane , linkage (software) , medicinal chemistry , organic chemistry , alkyl , psychology , biochemistry , psychotherapist , gene
The indolyl sulfide compounds ( 5,6,7,8 ) gave 3‐3′‐diindole methane derivatives by a double decomposition‐displacement reaction. These same compounds when reacted with alkoxides yielded 3‐alkoxy‐methylindole derivatives ( 9‐14 ).
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom