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Stille Coupling and One-pot Reduction-Deprotection Sequence in Preparing Z-3-(2-Amino-phenyl)-prop-2-en-1-ol, a Precursor in Quinoline Synthesis

Wilfred, Cecilia (2008) Stille Coupling and One-pot Reduction-Deprotection Sequence in Preparing Z-3-(2-Amino-phenyl)-prop-2-en-1-ol, a Precursor in Quinoline Synthesis. [Citation Index Journal]

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Abstract

Stille coupling on N-(2-iodo-phenyl)-acetamide followed by reduction-deprotection sequence has been utilised to prepare Z-3-(2-amino-phenyl)-prop-2-en-1-ol (1). Consequently, tandem oxidation processes on Z

Item Type:Citation Index Journal
Subjects:Q Science > QD Chemistry
Departments / MOR / COE:Departments > Fundamental & Applied Sciences
ID Code:7859
Deposited By: Assoc Prof Cecilia Devi Wilfred
Deposited On:14 Aug 2012 03:09
Last Modified:19 Jan 2017 08:26

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