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A Facile One-Pot Conversion of Acetates of the Baylis−Hillman Adducts to [ E ]-α-Methylcinnamic Acids

✍ Scribed by Basavaiah, Deevi; Krishnamacharyulu, Marimganti; Hyma, Rachakonda Suguna; Sarma, Pakala K. S.; Kumaragurubaran, Nagaswamy


Book ID
121356109
Publisher
American Chemical Society
Year
1999
Tongue
English
Weight
165 KB
Volume
64
Category
Article
ISSN
0022-3263

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One-pot facile conversion of the acetate
✍ Deevi Basavaiah; Tummanapalli Satyanarayana 📂 Article 📅 2002 🏛 Elsevier Science 🌐 French ⚖ 104 KB

A facile, one-pot convenient transformation of the acetates of Baylis-Hillman adducts into fused pyrimidones, i.e. 3-substituted-1,5-diazabicyclo(4.4.0)deca-2,5,7,9-tetraen-4-ones via reaction with 2-aminopyridine in environmentally friendly aqueous media is described.

A solvent-free protocol for one pot conv
✍ R. Sreevani; A. Manjula; B. Vittal Rao 📂 Article 📅 2011 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 134 KB

## Abstract A facile one pot transformation of Baylis Hillman acetates to pyrido[1,2‐a]pyrimidin‐2‐ones by reaction with 2‐amino pyridine in a total solvent‐free protocol is illustrated. The 3‐substituted‐2H‐pyrido[1,2‐a]pyrimidin‐2‐ones are obtained in pure form without involving any purification