The role of the C(2) configuration and methyl substitution on the catalytic activity of novel 2,3,3- and 2,7,7-trimethyl-substituted γ-aminonorbornan-2-ols-Reference-Cited by-同舟云学术

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The role of the C(2) configuration and methyl substitution on the catalytic activity of novel 2,3,3- and 2,7,7-trimethyl-substituted γ-aminonorbornan-2-ols

Published:2010 Issue: Volume: Page:NA-NA
ISSN:0899-0042
Container-title:Chirality
language:en
Short-container-title:Chirality

Author:

Martínez Antonio García,Vilar Enrique Teso,Fraile Amelia García,Cerero Santiago de la Moya,Ruiz Paloma Martínez,Morillo Cristina Díaz

Publisher

Wiley

Subject

Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry

Reference42 articles.

1. Enantioselective Catalysis;Bolm;Chem Rev,2003

2. Enantioselective addition of organometallic reagents to carbonyl compounds: chirality transfer, multiplication, and amplification;Noyori;Angew Chem Int Ed Engl,1991

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Deciphering the mechanism behind efficient enantioselective ethylation with thiazolidine‐based amino alcohols;Applied Organometallic Chemistry;2021-12-30

2. Electron ionization-induced fragmentation of bridgehead-substituted norbornan-2-ones derived from fenchone;International Journal of Mass Spectrometry;2013-01

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