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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 35, 2005 - Issue 7
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Original Articles

Facile Synthesis of 12‐Ketoquino[2,1‐b]Quinazolines via the Vilsmeier–Haack Reaction of 6‐Nitro‐2‐Methyl‐3‐Aryl‐4(3H)Quinazolones

Harjinder S. Bhatti Dyes Research Laboratory, University Institute of Chemical Technology, University of Mumbai, Matunga, Mumbai, India; Tytan Organics Pvt Ltd, C‐146, Pawne, Thane Belapur Road, Navi Mumbai, 400703, India
&
S. Seshadri Dyes Research Laboratory, University Institute of Chemical Technology, University of Mumbai, Matunga, Mumbai, India; 88, Ashtalakshmi, Bhaudaji Cross Road, Matunga, Mumbai, 400 019, IndiaCorrespondence[email protected]
Pages 907-912 | Received 17 Nov 2004, Published online: 21 Aug 2006

Citations (5)

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MahmoudR. Mahmoud & HamedA. Y. Derbala. (2010) Heteroannulated Quinazoline and Quinazolinone Derivatives from (Z)-2-[1-Benzamido-2-(3,4,5-trimethoxyphenyl)]vinyl-3,1-benzoxazin-4(3H)-one. Synthetic Communications 40:10, pages 1516-1529.
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Z.H. Li, B. Hong & W.K. Su. (2009) A Convenient Method for the Synthesis of 3,5,6-Trisubstituted-2-chloropyridines with bis-(Trichloromethyl) Carbonate. Organic Preparations and Procedures International 41:6, pages 533-538.
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Articles from other publishers (3)

Zerong Wang. 2010. Comprehensive Organic Name Reactions and Reagents. Comprehensive Organic Name Reactions and Reagents 2872 2879 .
Zerong Wang. 2010. Comprehensive Organic Name Reactions and Reagents. Comprehensive Organic Name Reactions and Reagents 1046 1050 .
Harjinder S. Bhatti & S. Seshadri. (2005) Facile Synthesis of 12‐Ketoquino [2,1‐b]Quinazolines via the Vilsmeier—Haack Reaction of 6‐Nitro‐2‐methyl‐3‐aryl‐4(3H)quinazolones.. ChemInform 36:35.
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