Mild reaction of pummerer rearrangement products with aromatic compounds in the presence of lewis acids. Application to the preparation of arylmethylene ketones, arylacetoesters, and arylacetonitriles.-Reference-Cited by-同舟云学术

Mild reaction of pummerer rearrangement products with aromatic compounds in the presence of lewis acids. Application to the preparation of arylmethylene ketones, arylacetoesters, and arylacetonitriles.

Published:1985-01 Issue:4 Volume:26 Page:477-480
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Stamos Ioannis K.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference22 articles.

1. Olefinic Cyclisations Initiated by Pummerer Rearrangement Products; Synthesis of Cyclic Ketones

2. Studies on intramolecular alkylation. XIII. The synthesis of 3,4-Dihydrophenanthren-2(1H)-ones from Pummerer intermediates

3. Pummerer reaction intermediate as an initiating function for cationic olefin cyclization

4. Synthesis of (.+-.)-10,22-dioxokopsane and (.+-.)-kopsanone, heptacyclic indole alkaloids. Synthetic and mechanistic studies

5. Indole-2,3-quinodimethan route to Aspidosperma alkaloids: synthesis of dl-aspidospermidine

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