Enantiotopic Differentiation of pro-R or pro-S Chlorides in (Dichloromethyl)borates by Chiral Lewis Acids: Enantioselective Synthesis of (α-Chloroalkyl)boronates-Reference-Cited by-同舟云学术

Enantiotopic Differentiation of pro-R or pro-S Chlorides in (Dichloromethyl)borates by Chiral Lewis Acids: Enantioselective Synthesis of (α-Chloroalkyl)boronates

Published:1997-01-01 Issue:4 Volume:119 Page:846-847
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Jadhav Prabhakar K.¹,Man Hon-Wah¹

Affiliation:

1. Chemical and Physical Sciences Department The Du Pont Merck Pharmaceutical Company Experimental Station, P. O. Box 80500 Wilmington, Delaware 19880-0500

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja9635185

Reference12 articles.

1. Recent advances in the boron route to asymmetric synthesis

2. Boronic ester homologation with 99% chiral selectivity and its use in syntheses of the insect pheromones (3S,4S)-4-methyl-3-heptanol and exo-brevicomin

3. (R,R)-2,3-Butanediol as chiral directing group in the synthesis of (S)-.alpha.-chloro boronic esters

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