Controlled Semihydrogenation of Aminoalkynes Using Ethylenediamine as a Poison of Lindlar's Catalyst
Author:
Affiliation:
1. Department of Process Research, Merck & Co., Inc., P.O. Box 2000, Rahway, New Jersey 07065 kevin_campos@merck.com
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo015514a
Reference21 articles.
1. Lindlar, H.; Dubuis, R.Organic Syntheses; Wiley: New York, 1973; Collect. Vol. V, pp 880−883.
2. Asymmetric, Stereocontrolled Total Synthesis of Paraherquamide A
3. Total Synthesis of the Novel, Immunosuppressive Agent (−)-Pateamine A from Mycale sp. Employing a β-Lactam-Based Macrocyclization
4. Prostaglandin Syntheses by Three-Component Coupling. New Synthetic Methods(49)
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