✦ LIBER ✦

New Reaction of Schiff Base with Dimedone: New Method for the Acridine Derivatives under Microwave Irradiation.

✍ Scribed by Shujiang Tu; et al. et al.

Publisher: John Wiley and Sons
Year: 2007
Weight: 23 KB
Volume: 38
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200723140

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

New reaction of schiff base with dimedon

New reaction of schiff base with dimedone: New method for the acridine derivatives under microwave irradiation

✍ Shujiang Tu; Tuanjie Li; Yan Zhang; Feng Shi; Jianing Xu; Qian Wang; Jinpeng Zha 📂 Article 📅 2007 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 390 KB 👁 1 views

## Abstract magnified image A novel cascade reaction of Schiff's base was described. The products afforded in the reaction depended on the ratio of the two starting materials. A possible mechanism of the reactions is proposed, which underwent the breaking and new formation of the bond between carb

ChemInform Abstract: Multicomponent Reac

ChemInform Abstract: Multicomponent Reactions for the Synthesis of New 3′-Indolyl Substituted Heterocycles under Microwave Irradiation.

✍ Song-Lei Zhu; Shun-Jun Ji; Kai Zhao; Yu Liu 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 41 KB 👁 2 views

A New and Efficient Method for the Synth

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

✍ Li-wen Xu; Fu-wei Li; Chun-gu Xia; Wei Sun 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 80 KB 👁 2 views

ChemInform Abstract: An Efficient Method

ChemInform Abstract: An Efficient Method for the Preparation of New Analogues of Leucettamine B under Solvent-Free Microwave Irradiation.

✍ Mansour Debdab; Steven Renault; Samar Eid; Olivier Lozach; Laurent Meijer; Franc 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 27 KB 👁 1 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

A Convenient, Rapid, and Highly Selectiv

A Convenient, Rapid, and Highly Selective Method for Synthesis of New Pyrazolo[1,5-a]pyrimidines via the Reaction of Enaminones and 5-Amino-1H-pyrazoles under Microwave Irradiation.

✍ Ming Li; Shuwen Wang; Lirong Wen; Huazheng Yang; Xiuli Zhang 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 18 KB 👁 1 views

A convenient, rapid, and highly selectiv

A convenient, rapid, and highly selective method for synthesis of new pyrazolo[1,5-a]pyrimidines via the reaction of enaminones and 5-amino-1H-pyrazoles under microwave irradiation

✍ Li Ming; Wang Shuwen; Wen Lirong; Yang Huazheng; Zhang Xiuli 📂 Article 📅 2005 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 76 KB

## Abstract Twelve new 7‐aryl‐3‐cyanopyrazolo[1,5‐__a__]pyrimidines (**3a‐f**) and ethyl 7‐arylpyrazolo[1,5‐__a__]pyrimidine‐3‐carboxylates (**3g‐l**) have been conveniently synthesized by the reaction of enaminones with 5‐amino‐1__H__‐pyrazoles in good yields under microwave irradiation. With one