Record Details

Design and synthesis of hybrid cyclophanes containing thiophene and indole units via Grignard reaction, Fischer indolization and ring-closing metathesis as key steps

DSpace at IIT Bombay

View Archive Info
 
 
Field Value
 
Title Design and synthesis of hybrid cyclophanes containing thiophene and indole units via Grignard reaction, Fischer indolization and ring-closing metathesis as key steps
 
Creator KOTHA, S
CHINNAM, AK
SHIRBHATE, ME
 
Subject DIVERSITY-ORIENTED APPROACH
AMINO-ACID DERIVATIVES
OLEFIN METATHESIS
STRATEGIES
COMPLEXES
PEPTIDES
SYSTEMS
cyclophane
Grignard reaction
Fischer indolization
ring-closing metathesis
 
Description We demonstrate a new synthetic strategy to cyclophanes containing thiophene and indole moieties via Grignard addition, Fischer indolization and ring-closing metathesis as key steps.
 
Publisher BEILSTEIN-INSTITUT
 
Date 2016-01-15T10:39:47Z
2016-01-15T10:39:47Z
2015
 
Type Article
 
Identifier BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY, 11,1514-1519
1860-5397
http://dx.doi.org/10.3762/bjoc.11.165
http://dspace.library.iitb.ac.in/jspui/handle/100/18369
 
Language en