Hydroxypinanone: Solute/solute interactions and non-linear chiroptical properties
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. The Hydroxypinanone as Chiral Auxiliary in Michael Additions: an Inversion of Diastereoselectivity at Low Concentration of Enolate, a Substrate-Directed Approach
2. A four-step, highly enantioselective synthesis and enzymatic resolution of 3,4-dichloro-phenylalanine.
3. A Four-Step Diastereoselective Synthesis of D-erythro-Sphingosine by an Enantioselective Aldol Reaction Using a Titanium Enolate Derived from a Chiral Iminoglycinate
4. Diastereoselective monoalkylation of lithium and potassium enolates of a chiral imine of ethyl glycinate: the role of added salts
5. Enantioselective synthesis of optically pure natural S(+) or unnatural R(-) DABA
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1. Optical purity, enantiomeric excess and the Horeau effect;Organic & Biomolecular Chemistry;2020
2. Chiral Aggregation, Equilibria, and the Horeau Effect;Chiroptical Spectroscopy;2016-08-23
3. Specific Optical Rotations and the Horeau Effect;Chirality;2015-12-28
4. Chiroptical Spectroscopy of Surfactants;The Journal of Physical Chemistry A;2012-05-17
5. Stereoselective Synthesis of γ-Fluorinated α-Amino Acids Using 2-Hydroxy-3-pinanone as an Auxiliary;European Journal of Organic Chemistry;2000-11
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