𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of substituted 1,2-dihydroisoquinolines by the intramolecular 1,3-dipolar alkyl azide-olefin cycloaddition

✍ Scribed by Liu, Jia Ming; Young, Jenn Jong; Li, Yu Jang; Sha, Chin Kang

Book ID
111917334
Publisher
American Chemical Society
Year
1986
Tongue
English
Weight
592 KB
Volume
51
Category
Article
ISSN
0022-3263

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

ChemInform Abstract: An Efficient Synthe
ChemInform Abstract: An Efficient Synthesis of (Pyrrolidin-2-ylidene)glycinate Using Intramolecular 1,3-Dipolar Cycloaddition of Azide and Olefin.
✍ Yaeko Konda; Takahiro Sato; Kaori Tsushima; Masataka Dodo; Ami Kusunoki; Masatak πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 31 KB πŸ‘ 1 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

Synthesis of tricyclic-2-aminoindoles by
Synthesis of tricyclic-2-aminoindoles by intramolecular 1,3-dipolar cycloaddition of 1-Ο‰-azidoalkylindoles
✍ Marco A de la Mora; Erick Cuevas; Joseph M Muchowski; Raymundo Cruz-Almanza πŸ“‚ Article πŸ“… 2001 πŸ› Elsevier Science 🌐 French βš– 60 KB

Thermolysis of the 1-v-azidoalkylindoles 4, bearing an electron attracting substituent at C-3 (CHO, COMe, COOMe, CN) provides imidazo[1,2-a]indoles (5, n=1), pyrimidino[1,2-a]indoles (5, n=2), and 1,3-diazepino[1,2-a]indoles (5, n=3).