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Synthesis of Indeno[2,1-a]pyrrolo[3,4-c]carbazole Lactam Regioisomers Using Ethyl cis-β-Cyanoacrylate as a Dienophile and Lactam Precursor.

✍ Scribed by Robert L. Hudkins; Chung Ho Park


Publisher
John Wiley and Sons
Year
2003
Weight
196 KB
Volume
34
Category
Article
ISSN
0931-7597

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✦ Synopsis


Abstract

For Abstract see ChemInform Abstract in Full Text.


📜 SIMILAR VOLUMES


Synthesis of indeno[2,1-a]pyrrolo[3,4-c]
✍ Robert L. Hudkins; Chung Ho Park 📂 Article 📅 2003 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 114 KB 👁 1 views

## Abstract Reported here is the synthesis and characterization of the indenopyrrolocarbazole ring system utilizing a Diels‐Alder reaction with 2‐indenylindole and maleimide. Clemmensen reduction of imide **10** furnished the 5‐oxo (**16**) and 7‐oxo (**17**) lactam regioisomers. A new regiospecifi

ChemInform Abstract: Staudinger and retr
✍ Lajos Fodor; Peter Csomos; Antal Csampai; Pal Sohar 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

## Abstract The title compounds (V), which cannot be obtained by direct oxidation of (I), are prepared using the reversible formation of a dichloro‐β‐lactam moiety as novel protecting group.