𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Regioselective π-extension of indoles with rhodium enalcarbenoids – synthesis of substituted carbazoles

✍ Scribed by Rathore, Kuldeep Singh; Harode, Mandeep; Katukojvala, Sreenivas

Book ID
126490202
Publisher
Royal Society of Chemistry
Year
2014
Tongue
English
Weight
681 KB
Volume
12
Category
Article
ISSN
1477-0520

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Novel regioselective synthesis of decahy
Novel regioselective synthesis of decahydrobenzocarbazoles using rhodium generated carbonyl ylides with indoles
✍ Sengodagounder Muthusamy; Chidambaram Gunanathan; Srinivasarao Arulananda Babu 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 74 KB

Intermolecular cycloadditions of five-membered cyclic carbonyl ylides 3 with indole, N-methylindole and N-benzylindole afforded decahydrobenzo[c]carbazole 4a-f or decahydrocyclopenta[c]carbazole 4g-h derivatives with high regioselectivity. With N-benzoylindole and N-sulphonylindole, decahydrobenzo[

One-Pot Synthesis of Substituted Dihydro
One-Pot Synthesis of Substituted Dihydroindeno[1,2-b]indoles and Dihydrobenzo[a]carbazoles by Photostimulated Reactions of o-Iodoaniline with Carbanions by the SRN1 Mechanism.
✍ Silvia M. Barolo; Cecire Rosales; Jorge E. Angel Guio; Roberto A. Rossi 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 23 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.

One pot synthesis of substituted dihydro
One pot synthesis of substituted dihydroindeno[1,2-b]indoles and dihydrobenzo[a]carbazoles by photostimulated reactions of o-iodoaniline with carbanions by the SRN1 mechanism
✍ Silvia M. Barolo; Roberto A. Rossi; Ceciréa Rosales; Jorge E. Angel Guío 📂 Article 📅 2006 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 309 KB

## Abstract magnified image The photostimulated reaction of enolate anions of cyclic aromatic ketones such as substituted indan‐1‐ones and 3,4‐dihydro‐2__H__‐naphthalen‐1‐one with __o__‐iodoaniline in DMSO affords 1‐, 2‐, 3‐, and 4‐methoxy‐5,10‐dihydroindeno[1,2‐__b__]indoles (34‐40%), 1,2‐, 1,4‐,