𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A New and Efficient Method for the Synthesis of 2,2′-Dibromo-1,1′-binaphthyl Under Microwave Irradiation

✍ Scribed by Xu, Li-wen; Li, Fu-wei; Xia, Chun-gu; Sun, Wei

Book ID
121272277
Publisher
Taylor and Francis Group
Year
2003
Tongue
English
Weight
157 KB
Volume
33
Category
Article
ISSN
0039-7911

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A rapid and efficient method for synthes
A rapid and efficient method for synthesis of pyrimido[1,2-a]-benzimidazole derivatives under microwave irradiation
✍ Qiya Zhuang; Chunmei Li; Shujiang Tu; Longji Cao; Dianxiang Zhou; Qingqing Shao; 📂 Article 📅 2008 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 281 KB

## Abstract magnified image A rapid and efficient method for synthesis pyrimido[1,2‐__a__]benzimidazole derivatives from readily available starting materials is accomplished under microwave irradiation. This method has the advantages of short reaction time, operational simplicity, increased safety

ChemInform Abstract: A Rapid and Efficie
ChemInform Abstract: A Rapid and Efficient Method for Synthesis of Pyrimido[1,2-a]benzimidazole Derivatives under Microwave Irradiation.
✍ Qiya Zhuang; Chunmei Li; Shujiang Tu; Longji Cao; Dianxiang Zhou; Qingqing Shao; 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 24 KB 👁 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

Efficient synthesis of 1,2,4-triazolo[4,
Efficient synthesis of 1,2,4-triazolo[4,3-a][1,8]naphthyridines under microwave irradiation
✍ K. Mogilaiah; T. Kumara Swamy; K. Shiva Kumar 📂 Article 📅 2009 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 56 KB 👁 1 views

## Abstract magnified image A simple and highly efficient procedure has been described for the synthesis of 6‐aryl‐9‐(4‐phenoxphenyl)‐1,2,4‐triazolo [4,3‐a] [1,8] napthyridines **(4)** by the oxidation of 4‐phenoxybenzaldehyde 3‐aryl‐1,8‐naphthyridin‐2‐ylhydrazones **(3)** with chloramines‐T in me