Record Details

Facile Synthesis of Tricyclic Oxazino- or Oxazepino-Fused Tetrahydroquinolines via Intramolecular Reductive Amidation

EPrints@IICB

View Archive Info
 
 
Field Value
 
Title Facile Synthesis of Tricyclic Oxazino- or Oxazepino-Fused
Tetrahydroquinolines via Intramolecular Reductive Amidation
 
Creator Mondal, Shyamal
Maity, Arindam
Naskar, Subhendu
Paira, Rupankar
Hazra, Abhijit
Sahu, Krishnendu B
Saha, Pritam
Das, Saktipada
Banerjee, Sukdeb
Mondal, Nirup B
 
Subject Chemistry
 
Description Reductive cyclization of w-(8-quinolyloxy)alkyl esters
by zinc in acetic acid is shown to constitute a convenient methodology
for the synthesis of oxazino- or oxazepino-fused tetrahydroquinolines.
It is operationally simple, requires a short reaction time,
and provides excellent yields.
 
Date 2011
 
Type Article
PeerReviewed
 
Format application/pdf
 
Identifier http://www.eprints.iicb.res.in/128/1/SYNTHESIS%2DSTUTTGART%2C13%2C_2079%2D2084%2C2011[30].pdf
Mondal, Shyamal and Maity, Arindam and Naskar, Subhendu and Paira, Rupankar and Hazra, Abhijit and Sahu, Krishnendu B and Saha, Pritam and Das, Saktipada and Banerjee, Sukdeb and Mondal, Nirup B (2011) Facile Synthesis of Tricyclic Oxazino- or Oxazepino-Fused Tetrahydroquinolines via Intramolecular Reductive Amidation. SYNTHESIS, 13. pp. 2079-2084.
 
Relation http://dx.doi.org/10.1055/s-0030-1260056
http://www.eprints.iicb.res.in/128/