4.8 Article

Chiral Amplification with a Stereodynamic Triaryl Probe: Assignment of the Absolute Configuration and Enantiomeric Excess of Amino Alcohols

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 131, Issue 45, Pages 16360-+

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ja907741v

Keywords

-

Funding

  1. NSF [CHE-0910604]
  2. Direct For Mathematical & Physical Scien
  3. Division Of Chemistry [0910604] Funding Source: National Science Foundation

Ask authors/readers for more resources

A stereodynamic, axially chiral triaryl probe is locked into a single conformation upon condensation with two amino alcohol substrates. The welt-defined chiral amplification in the diimines formed results in intense Cotton effects at high wavelengths that can be used for in situ CD analysis of the absolute configuration and of cyclic and acyclic substrates.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available