Highly selective synthesis of (E)-N-aryl-N-(1-propenyl) ethanamides via isomerization of N-allyl ethanamides catalyzed by ruthenium complexes-Reference-Cited by-同舟云学术

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Highly selective synthesis of (E)-N-aryl-N-(1-propenyl) ethanamides via isomerization of N-allyl ethanamides catalyzed by ruthenium complexes

Published:2001-10 Issue:40 Volume:42 Page:7095-7098
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Krompiec Stanislaw,Pigulla Mariola,Szczepankiewicz Wojciech,Bieg Tadeusz,Kuznik Nikodem,Leszczynska-Sejda Katarzyna,Kubicki Maciej,Borowiak Teresa

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference38 articles.

1. Synthesis of Pyrrole Derivatives from 5,6-Dihydro-4H-1,2-oxazines via Reductive Deoxygenation by Use of Fe3(CO)12

2. Dramatically different photochemical behaviour of 1-aroyl-2-methylene piperidine and pyrrolidine derivatives. An expeditious synthesis of ruspolinone

3. Photocyclisation of enamides. Part 39. General strategy for the synthesis of pseudodistomins: synthesis of triacetates of (±)-tetrahydropseudodistomin and proposed structures of pseudodistomins A and B

4. Redox-photosensitised reactions. Part 6. Stereospecific ring cleavage of 1-phenoxy-1,2,2a,3,4,8b-hexahydrocyclobuta[a]naphthalene-8b-carbonitrile and its 2-methyl derivatives by redox-photosensitisation

5. N-Acyl Enamines in the Paternò–Büchi Reaction: Stereoselective Preparation of 1,2-Amino Alcohols by CC Bond Formation

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