Diene tricarbonyl iron complexes bearing a free diazo group. III.1 Synthesis of pyrazoles and chiral complexes with α-aminoacid or dienylcyclopropane substructures by 1,3-dipolar cycloaddition reactions
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Tricarbonyl Iron Complexes Bearing a Free Diazo Group. I. Synthesis and Cyclocarbonylation Reactions of α-Diazodiene Complexes
2. Migrations sigmatropiques [1,5] spontanees de groupes cetone, ester et nitrile en serie pyrazole. synthese d'un tricarbalcoxy-1,2,3 cyclopropene.
3. 1,3-Dipolare Addition cyclischer Diazoketone an Alkine und Cyclopropene. Heterocyclensynthese durch [1,5]-Acylwanderung
4. Spontaneous transpositions from pyrazolenines into pyrazoles. Competitive [1,5] migrations of an acyl or carbalkoxy group to the carbon and nitrogen.
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1. ChemInform Abstract: Diene Tricarbonyl Iron Complexes Bearing a Free Diazo Group. Part 3. Synthesis of Pyrazoles and Chiral Complexes with α-Aminoacid or Dienylcyclopropane Substructures by 1,3-Dipolar Cycloaddition Reactions.;ChemInform;2010-06-19
2. ASYMMETRIC 1,3-DIPOLAR CYCLOADDITIONS FOR THE CONSTRUCTION OF ENANTIOMERICALLY PURE HETEROCYCLES. A REVIEW;Organic Preparations and Procedures International;2001-04
3. Principal Component Analysis on the effect of nucleophiles on the reactivity of α-acylenaminoketones;Journal of the Chemical Society, Perkin Transactions 2;2001
4. Transition metals in organic synthesis: highlights for the year 1998 (25th Anniversary);Coordination Chemistry Reviews;2000-07
5. Chapter 5.4 Five Membered Ring Systems: With More than One N Atom;A Critical Review of the 1998 Literature preceded by two Chapters on Current Heterocyclic Topics;1999
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