𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ChemInform Abstract: Synthesis and hSERT Activity of Homotryptamine Analogues. Part 6. [3 + 2] Dipolar Cycloaddition of 3-Vinylindoles.

✍ Scribed by Lawrence R. Marcin; Ronald J. Mattson; Qi Gao; Dedong Wu; Thaddeus F. Molski; Gail K. Mattson; Nicholas J. Lodge


Publisher
John Wiley and Sons
Year
2010
Weight
23 KB
Volume
41
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

A series of homotryptamine analogues such as (V) and (VIII) is prepared via [3 + 2] dipolar cycloaddition of vinylindole (I) with cyclic nitrones as key step.


πŸ“œ SIMILAR VOLUMES


ChemInform Abstract: Intramolecular [3 +
✍ Masaharu Nakamura; Motoki Toganoh; Xio Qun Wang; Shigeru Yamago; Eiichi Nakamura πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons βš– 30 KB πŸ‘ 2 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v

ChemInform Abstract: [3 + 2] Cycloadditi
✍ G. PANDEY; T. D. BAGUL; A. K. SAHOO πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 35 KB πŸ‘ 1 views

3 + 2] Cycloaddition of Nonstabilized Azomethine Ylides. Part 7. Stereoselective Synthesis of Epibatidine and Analogues. -The key step in the synthesis of epibatidine (VII) and analogues like (VIII) and (XII) is the stereoselective [3 + 2] cycloaddition of the azomethine ylides (III) and (X). -(

ChemInform Abstract: Dipolar Cycloadditi
✍ A. P. KOZIKOWSKI; G. L. ARALDI; R. G. BALL πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 32 KB πŸ‘ 2 views

Dipolar Cycloaddition Route to Diverse Analogues of Cocaine: The 6-and 7-Substituted 3-Phenyltropanes. -In the search for antagonists or partial agonists of cocaine, 3-phenyltropanes of the types (VIII), (XI), and (XII) are prepared via tropenones of type (III)-(VI), obtained by dipolar cycloadditio