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Enantioselective Strecker Reaction (enantioselective + strecker_reaction)

Distribution by Scientific Domains
Chemistry100%

Selected Abstracts

ChemInform Abstract: Facile and Efficient Enantioselective Strecker Reaction of Ketimines by Chiral Sodium Phosphate.

CHEMINFORM, Issue 42 2009
Ke Shen
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source]

ChemInform Abstract: Highly Enantioselective Strecker Reaction of Ketoimines Catalyzed by an Organocatalyst from (S)-BINOL and L-Prolinamide.

CHEMINFORM, Issue 37 2008
Zongrui Hou
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source]

Catalytic Enantioselective Strecker Reaction of Ketoimines.

CHEMINFORM, Issue 36 2003
Shuji Masumoto
Abstract For Abstract see ChemInform Abstract in Full Text. [source]

Asymmetric Strecker Reaction of Ketoimines Catalyzed by a Novel Chiral Bifunctional N,N, -Dioxide

ADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 18 2006
Xiao Huang
Abstract A novel bifunctional N,N, -dioxide derived from L -prolinamide was employed to catalyze the enantioselective Strecker reaction of a range of N -tosyl ketoimines, and an effective additive was used to improve the reactivity (up to 99,% yield) as well as the enantioselectivity (up to 91,% ee). In addition, a rational transition state was proposed to elucidate the origin of chiral induction in which an S -adduct was produced. [source]