Synthesis of spiro[2H-indole-2,1′-1H-isoindole]-3,3′-diones, spiro[1H-isobenzofuran-1,2′-2H-indole]-3,3′-diones and spiro[benzofuran-2,1′-isobenzofuran]-3,3′-dionesviatransannular reactions of eight membered ring intermediates-Reference-Cited by-同舟云学术

Synthesis of spiro[2H-indole-2,1′-1H-isoindole]-3,3′-diones, spiro[1H-isobenzofuran-1,2′-2H-indole]-3,3′-diones and spiro[benzofuran-2,1′-isobenzofuran]-3,3′-dionesviatransannular reactions of eight membered ring intermediates

Published:1998-03 Issue:2 Volume:35 Page:397-403
ISSN:0022-152X
Container-title:Journal of Heterocyclic Chemistry
language:en
Short-container-title:

Author:

Bullington James L.,Dodd John H.

Publisher

Wiley

Subject

Organic Chemistry

Reference12 articles.

1. Synthesis of tetrahydroindeno[1,2-b]indol-10-ones and their rearrangement to [2]benzopyrano[4,3-b]indol-5-ones

2. Contrary to the findings of Black et al. [9] we confirmed this reaction proceeds uneventfully as long as pure 3,4,5-trimethoxyaniline is used.

3. M. Hooper and S. H. Imam, J. Chem. Soc. Perkin Trans. I, 1583 (1985).

4. Transannular Reactions of Peptides. The Peptide Nitrogen in a 10-Membered Ring1,2

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