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Synthesis of Chiral Ligands from Hydrindene Diols with a Consecutive Heterodomino Transformation as the Key Reaction Step
Author(s) -
Finet Laure,
Dakir Mohamed,
Castellote Isabel,
Kaoudi Talbi,
Toupet Loïc,
Arseniyadis Siméon
Publication year - 2007
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.200600730
Subject(s) - chemistry , domino , denticity , octane , combinatorial chemistry , bicyclic molecule , enantioselective synthesis , catalysis , cascade reaction , stereochemistry , organic chemistry , metal
We report here the elaboration of a bicyclo[2.2.2]octane system, synthesized by a consecutive domino process, towards highly functionalized stereopure derivatives, which could be used as multidentate ligands for the generation of asymmetric catalysts. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)