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Modular Synthesis of Furans with up to Four Different Substituents by a trans ‐Carboboration Strategy
Author(s) -
Jin Hongming,
Fürstner Alois
Publication year - 2020
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.202005560
Subject(s) - regioselectivity , chemistry , pinacol , furan , acylation , propargyl , medicinal chemistry , borylation , modularity (biology) , substituent , catalysis , combinatorial chemistry , organic chemistry , alkyl , biology , aryl , genetics
Propargyl alcohols, on treatment with MHMDS (M=Na, K), B 2 (pin) 2 , an acid chloride and a palladium/copper co‐catalyst system, undergo a reaction cascade comprised of trans ‐diboration, regioselective acylation, cyclization and dehydration to give trisubstituted furylboronic acid pinacol ester derivatives in good yields; subsequent Suzuki coupling allows a fourth substituent of choice to be introduced and hence tetrasubstituted (arylated) furans to be formed. In terms of modularity, the method seems unrivaled, not least because each product can be attained by two orthogonal but convergent ways (“diagonal split”). This asset is illustrated by the “serial” formation of a “library” of all twelve possible furan isomers that result from systematic permutation of four different substituents about the heterocyclic core.