Directed ortho metalation - cross coupling links. Carbamoyl rendition of the baker-venkataraman rearrangement. Regiospecific route to substituted 4-hydroxycoumarins-Reference-Cited by-同舟云学术

Directed ortho metalation - cross coupling links. Carbamoyl rendition of the baker-venkataraman rearrangement. Regiospecific route to substituted 4-hydroxycoumarins

Published:1998-07 Issue:28 Volume:39 Page:4995-4998
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kalinin Alexey V.,da Silva Alcides J.M.,Lopes Claudio C.,Lopes Rosangela S.C.,Snieckus Victor

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference33 articles.

1. Directed ortho metalation. Tertiary amide and O-carbamate directors in synthetic strategies for polysubstituted aromatics

2. The directed ortho lithiation of O-aryl carbamates. An anionic equivalent of the Fries rearrangement

3. Anionic Homologous Fries Rearrangement of O-(2-Methylaryl)carbamates. A Regiospecific Route to Benzo[b]furan-2(3H)-ones including an Unnamed Metabolite from Helenium Species

4. Remote directed metalation of biaryl o-carbamates. Ring to ring carbamoyl transfer route to biaryls, dibenzo[b,d]pyranones, and the natural fluorenone dengibsin

5. 322. Molecular rearrangement of some o-acyloxyacetophenones and the mechanism of the production of 3-acylchromones

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