Prediction of Catalyst and Substrate Performance in the Enantioselective Propargylation of Aliphatic Ketones by a Multidimensional Model of Steric Effects-Reference-Cited by-同舟云学术

Prediction of Catalyst and Substrate Performance in the Enantioselective Propargylation of Aliphatic Ketones by a Multidimensional Model of Steric Effects

Published:2013-02-11 Issue:7 Volume:135 Page:2482-2485
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Harper Kaid C.¹,Vilardi Sarah C.¹,Sigman Matthew S.¹

Affiliation:

1. Department of Chemistry, University of Utah, 315 South 1400 East, Salt Lake City, Utah 84112, United States

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja4001807

Reference44 articles.

1. Computer-Aided Design of Chiral Ligands. Part III. A Novel Ligand for Asymmetric Allylation Designed Using Computational Techniques

2. Computer-aided design of chiral ligands

3. Understanding Stereoinductionin Catalysis via Computer: New Tools for Asymmetric Synthesis

4. Updating the asymmetric osmium-catalyzed dihydroxylation (AD) mnemonic: Q2MM modeling and new kinetic measurements

5. Computer-Aided Design of Chiral Ligands. Part 2. Functionality Mapping as a Method To Identify Stereocontrol Elements for Asymmetric Reactions

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