Synthesis of Chiral Ligands from Hydrindene Diols with a Consecutive Heterodomino Transformation as the Key Reaction Step | Zendy

Finet Laure | Zendy; Dakir Mohamed | Zendy; Castellote Isabel | Zendy; Kaoudi Talbi | Zendy; Toupet Loïc | Zendy; Arseniyadis Siméon | Zendy

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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)

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