Vilsmeier formylation of para-substituted tert-anilines results in dibenzo[1,5]diazocines or quinazolinium salts: a remarkable example of the ‘t-amino effect’-Reference-Cited by-同舟云学术

Vilsmeier formylation of para-substituted tert-anilines results in dibenzo[1,5]diazocines or quinazolinium salts: a remarkable example of the ‘t-amino effect’

Published:1995 Issue:14 Volume: Page:1463-1464
ISSN:0022-4936
Container-title:J. Chem. Soc., Chem. Commun.
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Meth-Cohn Otto,Taylor David L.

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1995/C3/C39950001463

Reference22 articles.

1. A novel synthetic approach to mitomycins. One step synthesis of a 5,10-dioxo-1H -pyrrolo[1,2-a ]benz[f ]indole

2. Synthesis of pyrrolizines by intramolecular capture of 1,4-dipolar intermediates in reactions of enamines with dimethyl acetylenedicarboxylate

3. 1-Pyrrolidin-1-ylbuta-1,3-dienes as potential 1,5-dipoles; synthesis of pyrrolizines

4. Reactions of enamines with trifluoroacetic anhydride: trifluoroacetylation and the formation of 1,3-oxazines

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