erythro-1-Naphthyl-1-(2-piperidyl)methanol: Synthesis, Resolution, NMR Relative Configuration, and VCD Absolute Configuration-Reference-Cited by-同舟云学术

erythro-1-Naphthyl-1-(2-piperidyl)methanol: Synthesis, Resolution, NMR Relative Configuration, and VCD Absolute Configuration

Published:2003-08-21 Issue:19 Volume:68 Page:7308-7315
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Solladié-Cavallo A.¹,Marsol C.¹,Yaakoub M.¹,Azyat K.¹,Klein A.¹,Roje M.¹,Suteu C.¹,Freedman T. B.¹,Cao X.¹,Nafie L. A.¹

Affiliation:

1. Laboratoire de Stéréochimie Organométallique, ECPM/Université Louis Pasteur, 67087 Strasbourg, France, Chiral Technologies Europe, 67404 Illkirch, France, and Department of Chemistry, Syracuse University, Syracuse, New York 13244-4100

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0345502

Reference25 articles.

1. Enantioselective Hydrogenation of Ethyl Pyruvate over Pt/Alumina Modified by (R)-1-(1-Naphthyl)ethylamine Derivatives

2. 1-(1-Naphthyl)ethylamine and derivatives thereof as chiral modifiers in the enantioselective hydrogenation of ethyl pyruvate over Pt–alumina

3. Enantioselective hydrogenation of α-ketoesters with cinchona-modified platinum catalysts: Effect of acidic and basic solvents and additives

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