Facile Preparation of Some Highly Hindered Chiral 1,2-Diphenyl-2-(N-monoalkyl)amino Alcohols and N-Benzylbornamine
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397919208021619
Reference9 articles.
1. Asymmetric Synthesis Utilizing External Chiral Ligands
2. Asymmetric synthesis using homochiral lithium amide bases
3. Asymmetric synthesis of α-amino acids: Comparison of enolate vs. cation functionalization of N-BOC-5, 6-diphenyl-2,3,5,6-tetrahydro-4h-1,4-oxazin-2-ones
4. Camphor derivatives as chiral auxiliaries in asymmetric synthesis
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2. Preparation of some new derivatives of (1R,2S)-1,2-diphenyl-2-aminoethanol and enantioselective borane reduction of propiophenone;Chinese Journal of Chemistry;2010-08-27
3. ChemInform Abstract: Facile Preparation of Some Highly Hindered Chiral 1,2-Diphenyl-2-(N- monoalkyl)amino Alcohols and N-Benzylbornamine.;ChemInform;2010-08-21
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5. Synthesis of C2-symmetrical diamine based on (1R)-(+)-camphor and application to oxidative aryl coupling of naphthols;Tetrahedron: Asymmetry;2003-06
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