𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of Aristotelia-Type Alkaloids. Part XII. Total synthesis of (−)-tasmanine. Stereoelectronic factors that control the rearrangement of 3H-indol-3-ol derivatives to oxindoles ( = 1,3-dihydro-2H-indol-2-ones) or to pseudoindoxyls ( =1,2-dihydro-3H-indol-3-ones)

✍ Scribed by Rolf Güller; Hans-Jürg Borschberg


Publisher
John Wiley and Sons
Year
1993
Tongue
German
Weight
1004 KB
Volume
76
Category
Article
ISSN
0018-019X

No coin nor oath required. For personal study only.

✦ Synopsis


Part XII') Total Synthesis of (-


📜 SIMILAR VOLUMES


A Reinvestigation of the Oxidative Rearr
✍ Reto Stahl; Hans-Jürg Borschberg 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 German ⚖ 932 KB

Contrary to earlier reports, the base-induced rearrangement of the 7-hydroxy-7H-indolenines derived from ajmalicine (l), yohimbine (5), corynanthine (6), methyl reserpate (16), and methyl isoreserpate (17) in each case furnished not just one, but two epimeric spiro-pseudoindoxyl derivatives which ha

On the Reactions of Furan-2,3-diones wit
✍ Elif Korkusuz; İsmail Yıldırım 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 German ⚖ 235 KB

## Abstract Lactone analogues of 3‐substituted oxindoles (=1,3‐dihydro‐2__H__‐indol‐2‐ones) and nonbenzoid oxa‐analogous isoindigoid or nonbenzoid isoindigoid dyes were prepared by the reactions of furan‐2,3‐diones with oxindole and __Lawesson__ reagent (__Schemes 1__ and __3__), respectively. So,

One-pot synthesis of the indole derivati
✍ Barbara Ziobro; Barbara Sienkiewicz; Piotr Kowalski 📂 Article 📅 2004 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 110 KB

## Abstract New methods for the synthesis the indole derivative, Indapamide (1), using mixed anhydrides of the general formula R1COOCOOR2 (2) or DCC (N,N'‐dicyclohexylcarbodiimide) (3), are described.