Literature DB >> 18321122

Synthesis of fused 4,5-disubstituted indole ring systems by intramolecular friedel-crafts acylation of 4-substituted indoles.

Eric Fillion1, Aaron M Dumas.   

Abstract

4-Substituted indoles containing a variety of electrophiles and N-substituents undergo Friedel-Crafts acylation to give exclusively the products of cyclization at the 5-position of indole. These indanones and tetralones have been scarcely prepared and are subunits in natural products and analogues of potential biological significance.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18321122     DOI: 10.1021/jo702591p

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  3 in total

1.  Approaches to N-methylwelwitindolinone C isothiocyanate: facile synthesis of the tetracyclic core.

Authors:  Richard W Heidebrecht; Brian Gulledge; Stephen F Martin
Journal:  Org Lett       Date:  2010-06-04       Impact factor: 6.005

2.  2,2-Dimethyl-5-(2-nitro-benzyl-idene)-1,3-dioxane-4,6-dione.

Authors:  Fernando García-Álvarez; Nancy Romero; Carlos E Lobato-García; Joel L Terán; Angel Mendoza
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-12-08

3.  Regioselectivity of the SEAr-based cyclizations and SEAr-terminated annulations of 3,5-unsubstituted, 4-substituted indoles.

Authors:  Jonali Das; Sajal Kumar Das
Journal:  Beilstein J Org Chem       Date:  2022-03-08       Impact factor: 2.883

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.