Generation of Alkyl(dicarbonyl)(chloro)‐ruthenium Dimers in the Ruthenium‐Catalyzed Addition of Alkyl Formates to Ethylene | Zendy

Fabre Sylvie | Zendy; Kalck Philippe | Zendy; Lavigne Guy | Zendy

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Generation of Alkyl(dicarbonyl)(chloro)‐ruthenium Dimers in the Ruthenium‐Catalyzed Addition of Alkyl Formates to Ethylene

Author(s) -

Fabre Sylvie,

Kalck Philippe,

Lavigne Guy

Publication year - 1997

Publication title -

angewandte chemie international edition in english

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 5.831

H-Index - 550

eISSN - 1521-3773

pISSN - 0570-0833

DOI - 10.1002/anie.199710921

Subject(s) - alkyl , ruthenium , ethylene , formate , chemistry , catalysis , methyl formate , ethyl formate , stereospecificity , polymer chemistry , medicinal chemistry , photochemistry , organic chemistry

An ususual migration of the alkyl group away from the CO bond of added formate leads to strictly stereospecific formation of the stable ehtyl complex 2 when the catalytic addition of ethyl formate to ethylene (catalyst = 1 ) is terminated by freezing. Both ethylene and the alkyl formate act as sources of the alkyl groups and can thus be used for CC bond‐forming reactions below ambient temperature. PPN + = (Ph 3 P) 2 N + .

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