The Michael Addition of Enamines to Propenamidines. A Convenient Synthesis of 2β-Amidinoethylcyclo-Alkanones by Amidinoethylation Reaction
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397918908051067
Reference16 articles.
1. The Uncatalyzed Amidinoethylation of Alcohols by Their Michael-Type Addition to Propenamidines(1)
2. Amidinoethylation - A New Reaction; I. The Amidinoethylation of Thiols; A Facile Synthesis of 3-Alkylthio- and 3-Arylthiopropanamidines
3. Amidinoethylation - A New Reaction; II. The Amidinoethylation of Active Methylene Compounds; A Facile Synthesis of 3,3-Disubstituted 1,5-Pentanedicarboxamidines
4. Amidinoethylation—a new reaction—III
5. Amidinoethylation—a new reaction—IV
Cited by 3 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. Stork Reaction;Comprehensive Organic Name Reactions and Reagents;2010-09-15
2. The N-Amidinoethylation of 2-Aminoethanol by Michael Reaction with a N,N′-Disubstituted Propenamidine;Bulletin des Sociétés Chimiques Belges;2010-09-01
3. ChemInform Abstract: The Michael Addition of Enamines to Propenamidines. A Convenient Synthesis of 2-(β-Amidinoethyl)cycloalkanones by Amidinoethylation Reaction.;ChemInform;1990-03-13
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