Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/101492
Title: Synthesis of 2-aminofurans and 2-unsubstituted furans via carbenoid-mediated [3 + 2] cycloaddition
Authors: Jiang, Yaojia
Khong, Vanessa Zhong Yue
Lourdusamy, Emmanuvel
Park, Cheol-Min
Issue Date: 2012
Source: Jiang, Y., Khong, V. Z. Y., Lourdusamy, E., Park, C.-M. (2012). Synthesis of 2-aminofurans and 2-unsubstituted furans via carbenoid-mediated [3 + 2] cycloaddition. Chemical Communications, 48(25), 3133-3135.
Series/Report no.: Chemical communications
Abstract: An efficient dual synthetic manifold for 2-aminofurans and 2-unsubstituted furans has been developed. The carbenoid-mediated [3 + 2] cycloaddition of copper carbenoids with enamines provides 2-amino-2,3-dihydrofurans which serve as common intermediates for both 2-aminofurans and 2-unsubstituted furans.
URI: https://hdl.handle.net/10356/101492
http://hdl.handle.net/10220/11103
DOI: 10.1039/c2cc18139h
Rights: © 2012 The Royal Society of Chemistry.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SPMS Journal Articles

SCOPUSTM   
Citations 5

83
Updated on Jan 16, 2023

Web of ScienceTM
Citations 5

82
Updated on Jan 27, 2023

Page view(s) 50

447
Updated on Jan 31, 2023

Google ScholarTM

Check

Altmetric


Plumx

Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.