RUS  ENG
Full version
JOURNALS // Uspekhi Khimii // Archive

Usp. Khim., 2001 Volume 70, Issue 12, Pages 1175–1205 (Mi rcr783)

This article is cited in 25 papers

Structural and configurational relationships 'metal complex–substrate–product' in asymmetric catalytic hydrogenation, hydrosilylation and cross-coupling reactions

V. A. Pavlov

N. D. Zelinskii Institute of Organic Chemistry, Moscow

Abstract: The present-day published data on the relationships between the structures of rhodium, iridium, ruthenium, nickel and cobalt catalytic complexes and substrates in homogeneous asymmetric hydrogenation, hydrosilylation and cross-coupling reactions are systematised. The optimum ratio between the number of coordination vacancies in the complex and the number of functional groups of the substrate has been characterised in terms of a criterion of maximum enantioselectivity of the catalytic complex. The relationships between the configurations of the complexes and the products formed in the reactions are analysed. In the case of C2-symmetrical chiral diphosphine complexes as catalysts (some structural elements of their ligands represent an incomplete turn of a helix surrounding the central metal atoms), substrates of the same kind form the products having definite configurations characteristic of the particular orientation of the helix. For example, rhodium complexes with ligands that form an incomplete P-helical turn around metal atoms catalyse the formation of (R)-amino acids from the corresponding precursors. If the ligands contain fragments of M-helices around rhodium atoms, it is (S)-amino acids that are formed. The bibliography includes 234 references.

UDC: 547.466+542.971.2

Received: 25.04.2001

DOI: 10.1070/RC2001v070n12ABEH000676


 English version:
Russian Chemical Reviews, 2001, 70:12, 1037–1065

Bibliographic databases:


© Steklov Math. Inst. of RAS, 2024