Tetrahedron, volume 73, issue 5, pages 461-471
Palladium catalyzed asymmetric reactions assisted by P*,P*-bidentate bisdiamidophosphites based on 1,4-diols
Konstantin N. Gavrilov
1, 2, 3
,
Sergey V. Zheglov
1, 2, 3
,
Vladislav K Gavrilov
1, 2, 3
,
Marina G Maksimova
1, 2, 3
,
В. А. Тафеенко
4
,
V. V. Chernyshev
4
,
Kirill P. Birin
5
,
1
DEPARTMENT OF CHEMISTRY
3
46 Svoboda Street 390000 Ryazan Russian Federation
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Publication type: Journal Article
Publication date: 2017-02-01
Journal:
Tetrahedron
scimago Q3
SJR: 0.406
CiteScore: 3.9
Impact factor: 2.1
ISSN: 00404020, 14645416
Organic Chemistry
Drug Discovery
Biochemistry
Abstract
A small series of P*,P*-bidentate bisdiamidophosphite ligands containing 1,3,2-diazaphospholidine rings have been prepared. The cationic [Pd(allyl)(P*,P*)]BF4 and neutral [Pd(P*,P*)Cl2] palladium(II) complexes were synthesized with one of the new ligands. The use of these ligands provides up to 98% ee in Pd-catalyzed asymmetric allylations of (E)-1,3-diphenylallyl acetate, up to 72% ee in Pd-catalyzed asymmetric alkylation of cinnamyl acetate with ethyl 2-oxocyclohexane-1-carboxylate and up to 94% ee in Pd-catalyzed desymmetrization of N,N'-ditosyl-meso-cyclopent-4-ene-1,3-diol biscarbamate. The influence of the nature of the bridging ligand fragments of the bisdiamidophosphites on asymmetric induction is discussed.
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