Palladium catalyzed asymmetric hydrophosphination of α,β- and α,β,γ,δ-unsaturated malonate esters : efficient control of reactivity, stereo- and regio-selectivity

Both PC-cyclometalated and PCP-pincer type palladium catalysts have recently been found to be robust and efficacious catalysts for the asymmetric P–H addition reaction involving activated olefins. Our studies on the asymmetric P–H addition of diphenylphosphine to malonate ester and α,β,γ,δ-alkyliden...

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Main Authors: Leung, Pak-Hing, Yang, Xiang-Yuan, Gan, Jun Hao, Li, Yongxin, Pullarkat, Sumod A.
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2015
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Online Access:https://hdl.handle.net/10356/106744
http://hdl.handle.net/10220/25069
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1067442023-02-28T19:45:01Z Palladium catalyzed asymmetric hydrophosphination of α,β- and α,β,γ,δ-unsaturated malonate esters : efficient control of reactivity, stereo- and regio-selectivity Leung, Pak-Hing Yang, Xiang-Yuan Gan, Jun Hao Li, Yongxin Pullarkat, Sumod A. School of Physical and Mathematical Sciences DRNTU::Science::Chemistry::Inorganic chemistry::Metals Both PC-cyclometalated and PCP-pincer type palladium catalysts have recently been found to be robust and efficacious catalysts for the asymmetric P–H addition reaction involving activated olefins. Our studies on the asymmetric P–H addition of diphenylphosphine to malonate ester and α,β,γ,δ-alkylidenemalonate ester revealed for the first time that the catalyst choice can have a dramatic impact in terms of reactivity as well as regio- and stereo-control for this asymmetric hydrofunctionalization reaction. Besides showing significantly contrasting reactivity and stereoselectivity in the hydrophosphination reaction involving malonate ester, in the case of α,β,γ,δ-alkylidenemalonate ester, a novel regiodivergent method was developed with the 1,4-adduct being obtained exclusively with the PC-catalyst while the pincer catalyst produced only the 1,6-adduct. Accepted version 2015-02-16T09:09:28Z 2019-12-06T22:17:28Z 2015-02-16T09:09:28Z 2019-12-06T22:17:28Z 2015 2015 Journal Article Yang, X.-Y., Gan, J. H., Li, Y., Pullarkat, S. A., & Leung, P.-H. (2015). Palladium catalyzed asymmetric hydrophosphination of α,β- and α,β,γ,δ-unsaturated malonate esters : efficient control of reactivity, stereo- and regio-selectivity. Dalton trans., 44(3), 1258-1263. https://hdl.handle.net/10356/106744 http://hdl.handle.net/10220/25069 10.1039/C4DT02673J en Dalton transactions © 2015 The Author(s) (Published by Royal Society of Chemistry). This is the author created version of a work that has been peer reviewed and accepted for publication by Dalton Transactions, Royal Society of Chemistry. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1039/C4DT02673J]. 8 p. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic DRNTU::Science::Chemistry::Inorganic chemistry::Metals
spellingShingle DRNTU::Science::Chemistry::Inorganic chemistry::Metals
Leung, Pak-Hing
Yang, Xiang-Yuan
Gan, Jun Hao
Li, Yongxin
Pullarkat, Sumod A.
Palladium catalyzed asymmetric hydrophosphination of α,β- and α,β,γ,δ-unsaturated malonate esters : efficient control of reactivity, stereo- and regio-selectivity
description Both PC-cyclometalated and PCP-pincer type palladium catalysts have recently been found to be robust and efficacious catalysts for the asymmetric P–H addition reaction involving activated olefins. Our studies on the asymmetric P–H addition of diphenylphosphine to malonate ester and α,β,γ,δ-alkylidenemalonate ester revealed for the first time that the catalyst choice can have a dramatic impact in terms of reactivity as well as regio- and stereo-control for this asymmetric hydrofunctionalization reaction. Besides showing significantly contrasting reactivity and stereoselectivity in the hydrophosphination reaction involving malonate ester, in the case of α,β,γ,δ-alkylidenemalonate ester, a novel regiodivergent method was developed with the 1,4-adduct being obtained exclusively with the PC-catalyst while the pincer catalyst produced only the 1,6-adduct.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Leung, Pak-Hing
Yang, Xiang-Yuan
Gan, Jun Hao
Li, Yongxin
Pullarkat, Sumod A.
format Article
author Leung, Pak-Hing
Yang, Xiang-Yuan
Gan, Jun Hao
Li, Yongxin
Pullarkat, Sumod A.
author_sort Leung, Pak-Hing
title Palladium catalyzed asymmetric hydrophosphination of α,β- and α,β,γ,δ-unsaturated malonate esters : efficient control of reactivity, stereo- and regio-selectivity
title_short Palladium catalyzed asymmetric hydrophosphination of α,β- and α,β,γ,δ-unsaturated malonate esters : efficient control of reactivity, stereo- and regio-selectivity
title_full Palladium catalyzed asymmetric hydrophosphination of α,β- and α,β,γ,δ-unsaturated malonate esters : efficient control of reactivity, stereo- and regio-selectivity
title_fullStr Palladium catalyzed asymmetric hydrophosphination of α,β- and α,β,γ,δ-unsaturated malonate esters : efficient control of reactivity, stereo- and regio-selectivity
title_full_unstemmed Palladium catalyzed asymmetric hydrophosphination of α,β- and α,β,γ,δ-unsaturated malonate esters : efficient control of reactivity, stereo- and regio-selectivity
title_sort palladium catalyzed asymmetric hydrophosphination of α,β- and α,β,γ,δ-unsaturated malonate esters : efficient control of reactivity, stereo- and regio-selectivity
publishDate 2015
url https://hdl.handle.net/10356/106744
http://hdl.handle.net/10220/25069
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