✦ LIBER ✦

A convenient approach to the synthesis of prenyl-, furo- and pyrano-quinoline alkaloids of the rutaceae

✍ Scribed by N. Shobana; P. Yeshoda; P. Shanmugam

Publisher: Elsevier Science
Year: 1989
Tongue: French
Weight: 374 KB
Volume: 45
Category: Article
ISSN: 0040-4020
DOI: 10.1016/0040-4020(89)80106-1

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A Convenient Synthesis of the Pyrrolo[3,

A Convenient Synthesis of the Pyrrolo[3,2-c]quinoline Core of Martinelline Alkaloids.

✍ Miklos Nyerges; Imre Fejes; Laszlo Toeke 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 2 views

## Abstract For Abstract see ChemInform Abstract in Full Text.

ChemInform Abstract: A Convenient Approa

ChemInform Abstract: A Convenient Approach to the Synthesis of Furo- and Thieno-[3,2-c]pyridine Derivatives.

✍ Hiroshi Maruoka; Fumi Okabe; Keishi Yamasaki; Eiichi Masumoto; Toshihiro Fujioka 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 35 KB 👁 2 views

ChemInform Abstract: A Simple and Conven

ChemInform Abstract: A Simple and Convenient Approach to the Friedlaender Synthesis of Pyrano[2,3-b]pyridines.

✍ Nagarajan Panneer Selvam; Thelagathoti Hari Babu; Paramasivan T. Perumal 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 2 views

The structures of vepridimerines A-D, fo

The structures of vepridimerines A-D, four new dimeric prenylated quinolone alkaloids from Vepris lousii and Oricia renieri (Rutaceae)

✍ T. Bonaventure Ngadjui; J. Foyere Ayafor; B. Lucas Sondengam; Joseph D. Connolly 📂 Article 📅 1982 🏛 Elsevier Science 🌐 French ⚖ 216 KB

Chemically Rational Approach to the Synt

Chemically Rational Approach to the Synthesis of Precursors of the “Prenyl” Fragment in Epothilones.

✍ F. A. Gimalova; Z. A. Yusupov; T. A. Maslova; M. S. Miftakhov 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 15 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, please click on HTML or PDF.

A convenient approach to the canthin-4-o

A convenient approach to the canthin-4-one ring system: Total synthesis of the alkaloids tuboflavine and norisotuboflavine

✍ Andreas Puzik; Franz Bracher 📂 Article 📅 2009 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 78 KB

## Abstract magnified image Canthin‐4‐one, as well as 5‐ and 6‐alkylcanthin‐4‐ones are readily available through reaction of 1‐acyl‐β‐carbolines with Bredereck's reagent or dimethylacetamide acetals in anhydrous DMF. The intermediate enaminoketones readily undergo cyclization to the canthin‐4‐ones