Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/101494
Title: Chiral phosphapalladacycles as efficient catalysts for the asymmetric hydrophosphination of substituted methylidenemalonate esters : direct access to functionalized tertiary chiral phosphines
Authors: Pullarkat, Sumod A.
Xu, Chang
Gan, Kennard Jun Hao
Hennersdorf, Felix
Li, Yongxin
Leung, Pak-Hing
Issue Date: 2012
Source: Xu, C., Gan, K. J. H., Hennersdorf, F., Li, Y., Pullarkat, S. A., & Leung, P.-H. (2012). Chiral Phosphapalladacycles as Efficient Catalysts for the Asymmetric Hydrophosphination of Substituted Methylidenemalonate Esters: Direct Access to Functionalized Tertiary Chiral Phosphines. Organometallics, 31(8), 3022–3026.
Series/Report no.: Organometallics
Abstract: A chiral palladacycle-promoted enantioselective asymmetric hydrophosphination of substituted methylidenemalonate esters using diphenylphosphine that provides direct access to chiral tertiary phosphines is reported. Screening of three easily accessible C,N and C,P palladacycles as catalysts for this synthetic scenario provided insights into critical factors in catalyst design that influence the activation and stereochemistry in Pd(II)-catalyzed asymmetric P–H addition reactions involving such activated substrates.
URI: https://hdl.handle.net/10356/101494
http://hdl.handle.net/10220/13698
DOI: http://dx.doi.org/10.1021/om201115n
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SPMS Journal Articles

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