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HERO ID
8497048
Reference Type
Journal Article
Title
A novel method for synthesis of tetrahydro-2H-oxazolo[2,3-a]isoquinolines
Author(s)
Dinesha, HE; Sandhya, NC; Mantelingu, K
Year
2019
Is Peer Reviewed?
Yes
Journal
Asian Journal of Chemistry
ISSN:
0970-7077
EISSN:
0975-427X
Publisher
Chemical Publishing Co.
Volume
31
Issue
2
Page Numbers
403-409
Language
English
DOI
10.14233/ajchem.2019.21673
Abstract
An efficient and direct method for the synthesis of tetrahydro-2H-oxazolo[2,3-a]isoquinolines is reported. This novel method involves â¢3P mediated in situ oxidation of benzyl alcohols to aldehyde followed by acetic acid mediated [3+2] cycloaddition reaction to afford tetrahydro-2H-oxazolo[2,3-a]isoquinolines in one-pot operation with good to excellent yields. Heterocyclic alcohols also underwent the reaction with tetrahydroquinolines at room temperature. © 2018 Chemical Publishing Co. All rights reserved.
Keywords
C-H functionalization; Isoquinolines; [3+2] cycloaddition; â¢T3P
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