Asymmetric Intramolecular Buchner Reaction: From High Stereoselectivity to Coexistence of Norcaradiene, Cycloheptatriene, and an Intermediate Form in the Solid State
Author(s) -
Benjamin Darses,
Pascale Maldivi,
Christian Philouze,
Philippe Dauban,
JeanFrançois Poisson
Publication year - 2021
Publication title -
organic letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.94
H-Index - 239
eISSN - 1523-7060
pISSN - 1523-7052
DOI - 10.1021/acs.orglett.0c03774
Subject(s) - cycloheptatriene , stereocenter , intramolecular force , chemistry , valence (chemistry) , bicyclic molecule , stereoselectivity , stereochemistry , solid state , crystal structure , crystallography , computational chemistry , enantioselective synthesis , organic chemistry , catalysis
Bicyclic compounds bearing a quaternary stereogenic center have been obtained using asymmetric intramolecular Buchner reaction with excellent yields and level of enantioselectivity. X-ray crystallography determination of the absolute configuration of one product has led to the serendipitous observation of an unusual behavior within the crystal structure, with equilibrating norcaradiene and cycloheptatriene valence isomers at the solid state, as well as an even more unexpected intermediate form. DFT calculations were performed to support these observations.
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