Conversion of homochiral amines and α-amino esters to their chiral 1,2,3,5-substituted pyrrole derivatives via gold-catalysed amination/annulation reactions of 2-propynyl-1,3-dicarbonyl compounds-Reference-Cited by-同舟云学术

Conversion of homochiral amines and α-amino esters to their chiral 1,2,3,5-substituted pyrrole derivatives via gold-catalysed amination/annulation reactions of 2-propynyl-1,3-dicarbonyl compounds

Published:2001-10 Issue:19 Volume:12 Page:2715-2720
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Arcadi Antonio,Di Giuseppe Sabrina,Marinelli Fabio,Rossi Elisabetta

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference25 articles.

1. For a review of methods for the synthesis of pyrroles, see: Black, D. St. C. In Science of Synthesis; Mass, G., Ed.; Georg Thieme Verlag: Stuttgart, New York, 2001; Vol. 9, pp. 441–552.

2. A Novel Cu-Assisted Cycloisomerization of Alkynyl Imines: Efficient Synthesis of Pyrroles and Pyrrole-Containing Heterocycles

3. Samarium diiodide promoted reactions of a diphenyl α-iminoketone, a new synthesis of some pyrrole derivatives

4. Synthesis of alkyl-substituted pyrroles by three-component coupling of carbonyl compound, amine and nitro-alkane/alkene on a solid surface of silica gel/alumina under microwave irradiation

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