✦ LIBER ✦

Synthesis of deoxy derivatives of the glucosinolates glucotropaeolin and glucobrassicin

✍ Scribed by Harald Streicher; Laurent Latxague; Torsten Wiemann; Patrick Rollin; Joachim Thiem

Publisher: Elsevier Science
Year: 1995
Tongue: English
Weight: 817 KB
Volume: 278
Category: Article
ISSN: 0008-6215
DOI: 10.1016/0008-6215(95)00265-0

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of [3H]-labelled glucobrassici

Synthesis of [3H]-labelled glucobrassicin, a potential radiotracer for metabolic studies of indole glucosinolates

✍ S. Chevolleau; B. Joseph; P. Rollin; J. Tulliez 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 French ⚖ 401 KB

## Abstract Glucobrassicin, an indole glucosinolate widespread in cruciferous plants, appears to be involved in anticarcinogenic activity __via__ its breakdown products. In order to study the “in vivo” metabolism of glucobrassicin, we have synthesized the 5‐[^3^H]‐indol‐3‐ylmethyl glucosinolate (^3

ChemInform Abstract: Synthesis of 2-Deox

ChemInform Abstract: Synthesis of 2-Deoxy-2-fluoro-glucotropaeolin, a Thioglucosidase Inhibitor.

✍ S. COTTAZ; P. ROLLIN; H. DRIGUEZ 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 1 views

ChemInform Abstract: The First Synthesis

ChemInform Abstract: The First Synthesis of C-Glucotropaeolin

✍ V. Aucagne; D. Gueyrard; A. Tatibouet; S. Cottaz; H. Driguez; M. Lafosse; P. Rol 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 24 KB

The analysis of glucosinolates in Brassi

The analysis of glucosinolates in Brassica species using gas chromatography. Direct determination of the thiocyanate ion precursors, glucobrassicin and neoglucobrassicin

✍ Robert K. Heaney; G. Roger Fenwick 📂 Article 📅 1980 🏛 John Wiley and Sons 🌐 English ⚖ 435 KB

Synthesis and Biological Evaluation of 1

Synthesis and Biological Evaluation of 1-Deoxy-5-hydroxysphingosine Derivatives

✍ Judit Esteve; Adriana Lorente; Pedro Romea; Fèlix Urpí; Carla Ríos-Luci; José M. 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 230 KB 👁 1 views

A sequential transformation based on the titanium-mediated aldol addition of (S)-1-bromo-3-(tert-butyldimethylsilyloxy)-2-butanone, a chiral lactate-derived ketone, to tetradecanal followed by reduction of the ensuing aldolate afforded the corresponding syn-1,3-diol as a single diastereomer. Debro-[

Synthesis of the 4-, 6-deoxy, and 4,6-di

Synthesis of the 4-, 6-deoxy, and 4,6-dideoxy derivatives of d-mannose

✍ Toshiyuki Nishio; Yayoi Miyake; Koji Kubota; Mitsuru Yamai; Shigeru Miki; Teiich 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 314 KB

Dale et al. discussed the role of the hydroxyl groups in the interaction of sugars with the /3-glucosidase by investigating the inhibitory effects of some monosaccharides and their derivatives against the enzyme [1]. We planned to investigate the role of glycon hydroxyl groups via a kinetic study on