The bisected s-trans conformation-controlled highly stereoselective addition of Grignard reagents to C-cyclopropylaldonitrone. An efficient synthesis of 1-phenyl-2-[(S )-1-aminoalkyl]-N,N-diethylcyclopropanecarboxamides, a new class of potent NMDA receptor antagonists
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/2001/P1/B008230I
Cited by 13 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. ChemInform Abstract: The Bisected s-trans Conformation-Controlled Highly Stereoselective Addition of Grignard Reagents to C-Cyclopropylaldonitrone. An Efficient Synthesis of 1-Phenyl-2-[(S)-1-aminoalkyl]-N,N-diethylcyclopropanecarboxamides, a New Class of;ChemInform;2010-05-24
2. Alkylnitrogen Compounds: Compounds with NHalogen, NO, NS, NSe, and NTe Functional Groups;Comprehensive Organic Functional Group Transformations II;2005
3. Highly Stereoselective Grignard Addition to Cis-Substituted C-Cyclopropylaldonitrones. The Bisected s-Trans Transition State Can Be Stabilized Effectively by the Lewis Acid-Coordination;The Journal of Organic Chemistry;2004-11-17
4. The unusual 1,4-chelation-controlled nucleophilic addition to aldehydes with high stereoselectivity. A systematic study of stereoselectivity in the addition reaction of carbon nucleophiles to cis-substituted cyclopropanecarbaldehydes;Tetrahedron;2004-07
5. A Systematic Study of the Hydride Reduction of Cyclopropyl Ketones with Structurally Simplified Substrates. Highly Stereoselective Reductions of Trans-Substituted Cyclopropyl Ketones via the Bisected s-Cis Conformation;The Journal of Organic Chemistry;2003-04-05
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