𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Reduction of Indolin-2-ones and Desulfurization of Indoline-2-thiones to Indoline and Indole Derivatives

✍ Scribed by Takehiko Nishio; Norikazu Okuda; Choji Kashima

Publisher
John Wiley and Sons
Year
1990
Tongue
German
Weight
312 KB
Volume
73
Category
Article
ISSN
0018-019X

No coin nor oath required. For personal study only.

✦ Synopsis

1 9. VI. 90

📜 SIMILAR VOLUMES

Synthesis of Indole Derivatives by [2 +
Synthesis of Indole Derivatives by [2 + 2] Photocycloaddition of Indoline-2-thiones with alkenes and photodesulfurization of indoline-2-thiones
✍ Takehiko Nishio; Mitsuru Oka 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 German ⚖ 606 KB

The photochemical synthesis of indole derivatives starting from the indoline-2-thiones 1 is described. Irradiation of indoline-2-thiones 1 in the presence of alkenes 3 gave 2-alkyl-3H-indoles 4-7 or 2-alkylindoles 8-22 through the ring cleavage of the intermediates, spirocyclic amino-thietanes, init

Scavenging of reactive oxygen species by
Scavenging of reactive oxygen species by novel indolin-2-one and indoline-2-thione derivatives
✍ Hassan Y. Aboul-Enein; Aleksandra Kładna; Irena Kruk; Krzysztof Lichszteld; Tere 📂 Article 📅 2005 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 136 KB 👁 2 views

## Abstract The antioxidant behavior of a series of new synthesized substituted indoline‐2‐ones and indolin‐2‐thiones was investigated in this study using an oxygen radical absorbance capacity assay (ORAC$\_{ROO\mathop{\bullet}^{\!\!\!\!-}}$) and 2,2′‐azobis(2‐amidino‐propane) dihydrochloride (AAPH

Synthesis of indole and indolenine deriv
Synthesis of indole and indolenine derivatives starting from indoline-2-thiones
✍ Takehiko Nishio; Osamu Saku; Hiroshi Yamamoto 📂 Article 📅 2001 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 48 KB

## Abstract Indoline‐2‐thiones **1a‐b,d,f,h**, which have at least one hydrogen at the 3‐position reacted with α‐halo ester **2a‐d**, α‐halo ketones **2e‐f**, and a‐bromoacetonitrile **2g** to give 2‐alkylthioindole derivatives **3–11**. In a similar manner treatment of 3,3‐disubstituted indoline‐2