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Title: Origins of the enantioselectivity of a palladium catalyst with BINOL–phosphoric acid ligands

Abstract

The enantioselectivity of the studied C–H activation is related to the Brønsted acidity and isopropyl groups of the effective catalysts.

Authors:
ORCiD logo [1]
  1. Department of Chemistry, University of Illinois at Urbana–Champaign, Urbana, USA
Publication Date:
Sponsoring Org.:
USDOE
OSTI Identifier:
1479124
Resource Type:
Publisher's Accepted Manuscript
Journal Name:
Organic and Biomolecular Chemistry
Additional Journal Information:
Journal Name: Organic and Biomolecular Chemistry Journal Volume: 16 Journal Issue: 43; Journal ID: ISSN 1477-0520
Publisher:
Royal Society of Chemistry (RSC)
Country of Publication:
United Kingdom
Language:
English

Citation Formats

Zhang, Jun. Origins of the enantioselectivity of a palladium catalyst with BINOL–phosphoric acid ligands. United Kingdom: N. p., 2018. Web. doi:10.1039/C8OB02271B.
Zhang, Jun. Origins of the enantioselectivity of a palladium catalyst with BINOL–phosphoric acid ligands. United Kingdom. doi:10.1039/C8OB02271B.
Zhang, Jun. Wed . "Origins of the enantioselectivity of a palladium catalyst with BINOL–phosphoric acid ligands". United Kingdom. doi:10.1039/C8OB02271B.
@article{osti_1479124,
title = {Origins of the enantioselectivity of a palladium catalyst with BINOL–phosphoric acid ligands},
author = {Zhang, Jun},
abstractNote = {The enantioselectivity of the studied C–H activation is related to the Brønsted acidity and isopropyl groups of the effective catalysts.},
doi = {10.1039/C8OB02271B},
journal = {Organic and Biomolecular Chemistry},
number = 43,
volume = 16,
place = {United Kingdom},
year = {2018},
month = {11}
}

Journal Article:
Free Publicly Available Full Text
Publisher's Version of Record
DOI: 10.1039/C8OB02271B

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Cited by: 2 works
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