Asymmetric Synthesis of Bis(tertiary arsines): Highly Stereoselective Alkylations of Diastereomers of a Chiral Phosphine-Stabilized Bis(arsenium triflate)-Reference-Cited by-同舟云学术

Asymmetric Synthesis of Bis(tertiary arsines): Highly Stereoselective Alkylations of Diastereomers of a Chiral Phosphine-Stabilized Bis(arsenium triflate)

Published:2009-06-25 Issue:15 Volume:48 Page:7482-7490
ISSN:0020-1669
Container-title:Inorganic Chemistry
language:en
Short-container-title:Inorg. Chem.

Author:

Weir Michelle L.¹,Cade Ian A.¹,Kilah Nathan L.¹,Zhou Xiangting¹,Wild S. Bruce¹

Affiliation:

1. Research School of Chemistry, Institute of Advanced Studies, Australian National University, Canberra, ACT 0200, Australia

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ic900797y

Reference48 articles.

1. Asymmetric Catalytic Hydrogenation with an Optically Active Phosphinerhodium Complex in Homogeneous Solution

2. Catalytic asymmetric hydrogenation employing a soluble, optically active, rhodium complex

3. Catalytic asymmetric hydrogenation

4. Asymmetric hydrogenation. Rhodium chiral bisphosphine catalyst

5. Asymmetric catalytic reduction with transition metal complexes. I. Catalytic system of rhodium(I) with (-)-2,3-0-isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)butane, a new chiral diphosphine

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