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Exploiting the Multidentate Nature of Chiral Disulfonimides in a Multicomponent Reaction for the Asymmetric Synthesis of Pyrrolo[1,2‐ a ]indoles: A Remarkable Case of Enantioinversion
Author(s) -
Galván Alicia,
GonzálezPérez Adán B.,
Álvarez Rosana,
de Lera Angel R.,
Fañanás Francisco J.,
Rodríguez Félix
Publication year - 2016
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201511231
Subject(s) - enantioselective synthesis , steric effects , chemistry , catalysis , denticity , brønsted–lowry acid–base theory , context (archaeology) , computational chemistry , transition state , stereochemistry , chirality (physics) , combinatorial chemistry , organic chemistry , crystal structure , physics , paleontology , nambu–jona lasinio model , chiral symmetry breaking , quantum mechanics , biology , quark
A new multicomponent coupling reaction for the enantioselective synthesis of pyrrolo[1,2‐ a ]indoles under the catalysis of a chiral disulfonimide is described. The high specificity of the reaction is a consequence of the multidentate character of the Brønsted acid catalyst. Insights from DFT calculations helped explain the unexpected high enantioselectivity observed with the simplest 3,3′‐unsubstituted binaphthyl catalyst as a result of transition‐state stabilization by a network of cooperative noncovalent interactions. The remarkable enantioinversion resulting from the simple introduction of substituents at 3‐ and 3′‐positions, the first reported example of this phenomenon in the context of binaphthalene‐derived Brønsted acid catalysis, was instead attributed to destabilizing steric interactions.