Ontology highlight
ABSTRACT:
SUBMITTER: Romanini S
PROVIDER: S-EPMC4832839 | biostudies-literature | 2015 Dec
REPOSITORIES: biostudies-literature
Romanini Simone S Galletti Emilio E Caruana Lorenzo L Mazzanti Andrea A Himo Fahmi F Santoro Stefano S Fochi Mariafrancesca M Bernardi Luca L
Chemistry (Weinheim an der Bergstrasse, Germany) 20151021 49
A domino Friedel-Crafts/nitro-Michael reaction between 4-substituted indoles and nitroethene is presented. The reaction is catalyzed by BINOL-derived phosphoric acid catalysts, and delivers the corresponding 3,4-ring-fused indoles with very good results in terms of yields and diastereo- and enantioselectivities. The tricyclic benzo[cd]indole products bear a nitro group at the right position to serve as precursors of ergot alkaloids, as demonstrated by the formal synthesis of 6,7-secoagroclavine ...[more]