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Novel Petasis boronic acid reactions with indoles: synthesis of indol-3-yl-aryl-acetic acids

✍ Scribed by Dinabandhu Naskar; Subhasish Neogi; Amrita Roy; Ashis Baran Mandal

Publisher
Elsevier Science
Year
2008
Tongue
French
Weight
202 KB
Volume
49
Category
Article
ISSN
0040-4039

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✦ Synopsis

Indoles can serve as substrates for the Petasis boronic acid-Mannich reaction, providing a practical synthetic route for C-C bond formation in a-(N-substituted indole)carboxylic acids. The scope and limitations of this method have been examined.

πŸ“œ SIMILAR VOLUMES

ChemInform Abstract: Novel Petasis Boron
ChemInform Abstract: Novel Petasis Boronic Acid Reactions with Indoles: Synthesis of Indol-3-yl-aryl-acetic Acids.
✍ Dinabandhu Naskar; Subhasish Neogi; Amrita Roy; Ashis Baran Mandal πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons βš– 35 KB πŸ‘ 2 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 of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v

Synthesis of 2-acylindole-3-acetic acids
Synthesis of 2-acylindole-3-acetic acids: a novel base-mediated indole synthesis
✍ Kazunari Nakao; Yoshinori Murata; Hiroki Koike; Chikara Uchida; Kiyoshi Kawamura πŸ“‚ Article πŸ“… 2003 πŸ› Elsevier Science 🌐 French βš– 93 KB

An efficient and expedient synthetic route to 2-acylindole-3-acetic acids is described. This work first demonstrates a one-pot room-temperature indole ring construction via the in situ generation of indoline intermediate.