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The Synthesis and Structure of Stibaindoles
Author(s) -
Buchwald Stephen L.,
Fisher Richard A.,
Foxman Bruce M.
Publication year - 1990
Publication title -
angewandte chemie international edition in english
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 0570-0833
DOI - 10.1002/anie.199007711
Subject(s) - simple (philosophy) , monomer , chemistry , mathematics , stereochemistry , organic chemistry , combinatorial chemistry , computational chemistry , philosophy , polymer , epistemology
A simple route to stibaindoles , reaction (a), leads to monomeric 1‐chloro‐ and 1‐phenylstibaindoles in yields of 71–86%. Interest in heterocyclic compounds of heavy main‐group elements has increased dramatically in recent years owing to their uses in materials science. Y,Z = H, OMe, C 4 H 4