Record Details

Diversity-oriented approach to natural product inspired pyrano-carbazole derivatives: strategic utilization of hetero-Diels-Alder reaction, Fischer indolization and the Suzuki-Miyaura cross-coupling reaction

DSpace at IIT Bombay

View Archive Info
 
 
Field Value
 
Title Diversity-oriented approach to natural product inspired pyrano-carbazole derivatives: strategic utilization of hetero-Diels-Alder reaction, Fischer indolization and the Suzuki-Miyaura cross-coupling reaction
 
Creator KOTHA, S
ALI, R
SAIFUDDIN, M
 
Subject NONREARRANGED MONOTERPENOID UNIT
SIMPLE INDOLE ALKALOIDS
PRIVILEGED STRUCTURES
MOLECULAR FRAMEWORKS
OLEFIN METATHESIS
KEY STEPS
CHEMISTRY
CORE
SUBSTRUCTURES
SPIROCYCLES
1,3-Diketones
Fischer indolization
Hetero-Diels-Alder reaction
Pyrano-carbazoles
Styrenes
Suzuki-Miyaura cross-coupling reaction
 
Description A variety of natural products inspired pyrano-carbazole derivatives have been assembled via hetero-Diels-Alder reaction and Fischer indolization (FI) under operationally simple reaction conditions. Later, the scope of this methodology has been expanded through Suzuki-Miyaura cross-coupling reaction involving different boronic acids. This simple strategy can be useful to generate a variety of medicinally important carbazole derivatives. (C) 2015 Elsevier Ltd. All rights reserved.
 
Publisher PERGAMON-ELSEVIER SCIENCE LTD
 
Date 2016-01-15T05:54:03Z
2016-01-15T05:54:03Z
2015
 
Type Article
 
Identifier TETRAHEDRON, 71(47)9003-9011
0040-4020
http://dx.doi.org/10.1016/j.tet.2015.09.044
http://dspace.library.iitb.ac.in/jspui/handle/100/17865
 
Language en