𝔖 Bobbio Scriptorium
✦   LIBER   ✦

First synthesis of an O-glycosylated glucosinolate isolated from Moringa oleifera

✍ Scribed by D. Gueyrard; J. Barillari; R. Iori; S. Palmieri; P. Rollin

Publisher
Elsevier Science
Year
2000
Tongue
French
Weight
83 KB
Volume
41
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis

Starting from L-rhamnose, the first synthesis of the major glucosinolate (1) isolated from Moringa oleifera seeds was effected in seven steps.

πŸ“œ SIMILAR VOLUMES

ChemInform Abstract: First Synthesis of
ChemInform Abstract: First Synthesis of an O-Glycosylated Glucosinolate Isolated from Moringa oleifera.
✍ D. Gueyrard; J. Barillari; R. Iori; S. Palmieri; P. Rollin πŸ“‚ Article πŸ“… 2001 πŸ› John Wiley and Sons βš– 30 KB πŸ‘ 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 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

First synthesis of astilbin, biologicall
First synthesis of astilbin, biologically active glycosyl flavonoid isolated from Chinese folk medicine
✍ Ken Ohmori; Hiroki Ohrui; Keisuke Suzuki πŸ“‚ Article πŸ“… 2000 πŸ› Elsevier Science 🌐 French βš– 253 KB

A synthetic route to a biologically active glycosyl Β―avonoid, astilbin (1), was developed. The tetra-benzyl ether 4, derived from (+)-catechin, was glycosylated with the l-rhamnosyl donor 10 by using Cp 2 HfCl 2 Β± AgClO 4 , and subsequent oxidation of the C(4) position of the Β―avan skeleton followed

The first synthesis of (Β±)-brevione B, a
The first synthesis of (Β±)-brevione B, an allelopathic agent isolated from Penicillium sp.
✍ Hirosato Takikawa; Manabu Hirooka; Mitsuru Sasaki πŸ“‚ Article πŸ“… 2003 πŸ› Elsevier Science 🌐 French βš– 147 KB

Breviones A E (1 5), allelopathic agents isolated from Penicillium brevicompactum Dierckx, are structurally unique pentacyclic or hexacyclic diterpenoid derivatives. The first synthesis of brevione B (2) was achieved by employing the double S N 2%-type tandem reaction as a key step.