A facile synthesis of 2-amino-3H-quinazolin-4-ones with tandem aza- Wittig reaction

Article abstract of DOI:10.1080/00397910008087195

2-Amino-3H-quinazolin-4-ones 8 were prepared from tandem aza-Wittig reaction of iminophosphorane 5 with aromatic isocyanate and nucleaphilic reagent HY in mild condition.

Full text of DOI:10.1080/00397910008087195

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Synthetic Communications: An
International Journal for Rapid
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Organic Chemistry
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A Facile Synthesis of 2-
Mino-3H-Quinazolin-4-Ones
with Tandem Aza-Wittig
Reaction
Ming-Wu Ding a , Gui-Ping Zeng a & Tian-Jie Wu a
a Institute of Organic Synthesis Central China Normal
University , Wuhan, 430079, P.R. China
Published online: 04 Dec 2007.
To cite this article: Ming-Wu Ding , Gui-Ping Zeng & Tian-Jie Wu (2000) A Facile
Synthesis of 2-Mino-3H-Quinazolin-4-Ones with Tandem Aza-Wittig Reaction, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 30:9, 1599-1604, DOI: 10.1080/00397910008087195
To link to this article: http://dx.doi.org/10.1080/00397910008087195
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