Unknown

Dataset Information

0

Synthesis of 1-[bis(trifluoromethyl)phosphine]-1'-oxazolinylferrocene ligands and their application in regio- and enantioselective Pd-catalyzed allylic alkylation of monosubstituted allyl substrates.


ABSTRACT: A class of novel, easily accessible and air-stable 1-[bis(trifluoromethyl)phosphine]-1'-oxazolinylferrocene ligands has been synthesized from ferrocene. It became apparent that these ligands can be used in the regio- and enantioselective Pd-catalyzed allylic alkylation of monosubstituted allyl substrates in a highly efficient manner. Excellent regio- and enantioselectivity could be obtained for a wide range of substrates.

SUBMITTER: Lai ZW 

PROVIDER: S-EPMC4077528 | biostudies-other | 2014

REPOSITORIES: biostudies-other

altmetric image

Publications

Synthesis of 1-[bis(trifluoromethyl)phosphine]-1'-oxazolinylferrocene ligands and their application in regio- and enantioselective Pd-catalyzed allylic alkylation of monosubstituted allyl substrates.

Lai Zeng-Wei ZW   Yang Rong-Fei RF   Ye Ke-Yin KY   Sun Hongbin H   You Shu-Li SL  

Beilstein journal of organic chemistry 20140530


A class of novel, easily accessible and air-stable 1-[bis(trifluoromethyl)phosphine]-1'-oxazolinylferrocene ligands has been synthesized from ferrocene. It became apparent that these ligands can be used in the regio- and enantioselective Pd-catalyzed allylic alkylation of monosubstituted allyl substrates in a highly efficient manner. Excellent regio- and enantioselectivity could be obtained for a wide range of substrates. ...[more]

Similar Datasets

| S-EPMC2536500 | biostudies-literature
| S-EPMC2925184 | biostudies-literature
| S-EPMC5213737 | biostudies-literature
| S-EPMC4640231 | biostudies-literature
| S-EPMC6050583 | biostudies-literature
| S-EPMC6499109 | biostudies-literature