𝔖 Bobbio Scriptorium
✦   LIBER   ✦

One-step conversion of flavanones into isoflavones: a new facile biomimetic synthesis of isoflavones

✍ Scribed by Takeshi Kinoshita; Koji Ichinose; Ushio Sankawa


Book ID
104221883
Publisher
Elsevier Science
Year
1990
Tongue
French
Weight
173 KB
Volume
31
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis


Sunsmuryr One-step &em&I conversion of flavanones into isoflavones by use of thallium trim&ate (TIN) is reported, and the mechanism of a 2.3~aryl migration in this reaction is discussed in relation to in vivo reamngement process of flavanone precursors in the isoflavone biosynthesis.


πŸ“œ SIMILAR VOLUMES


A Facile, One-Step Conversion of 6-O-Tri
✍ Dimitri Komiotis; George Agelis; Stella Manta; Niki Tzioumaki; Evangelia Tsoukal πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons βš– 25 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, please click on HTML or PDF.

ChemInform Abstract: A New Method for th
✍ Massimo Curini; Francesco Epifano; Maria Carla Marcotullio; Ornelio Rosati; Moni πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 31 KB πŸ‘ 2 views

Halo-Nitro Derivatives. -Use of wet basic alumina as support for Oxone (KHSO 5 ) and KBr is crucial for the conversion of oximes (I), (III), (V), and (VII) directly into the corresponding gem-bromo-nitro compounds. -