✦ LIBER ✦

Configuration of necine pyrroles — Toxic metabolites of pyrrolizidine alkaloids

✍ Scribed by Kedzierski, Bogdan; Buhler, Donald R.

Book ID: 122023637
Publisher: Elsevier Science
Year: 1985
Tongue: English
Weight: 275 KB
Volume: 25
Category: Article
ISSN: 0378-4274
DOI: 10.1016/0378-4274(85)90070-0

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Carcinogenicity of some pyrrolic pyrroli

Carcinogenicity of some pyrrolic pyrrolizidine alkaloid metabolites and analogues

✍ Mattocks, A.R.; Cabral, J.R.P. 📂 Article 📅 1982 🏛 Elsevier Science 🌐 English ⚖ 367 KB

Synthetic Compounds with Toxic Propertie

Synthetic Compounds with Toxic Properties similar to those of Pyrrolizidine Alkaloids and their Pyrrolic Metabolites

✍ MATTOCKS, A. R. 📂 Article 📅 1971 🏛 Nature Publishing Group 🌐 English ⚖ 226 KB

Simple procedures for preparing putative

Simple procedures for preparing putative toxic metabolites of pyrrolizidine alkaloids

✍ A.R. Mattocks; Jukes Rebekah; Brown Janet 📂 Article 📅 1989 🏛 Elsevier Science 🌐 English ⚖ 446 KB

Total synthesis of (±)-otonecine, a neci

Total synthesis of (±)-otonecine, a necine base of pyrrolizidine alkaloids

✍ Haruki Niwa; Youchi Uosaki; Kiyoyuki Yamada 📂 Article 📅 1983 🏛 Elsevier Science 🌐 French ⚖ 130 KB

&one&z (l\_), a hepfitinenAative necine base ad hepatoLotic and catroinog~tic py~~~oLLz~&ne aLkaLoL&, ~a6 nyntienized -in ~~~cemic dam #om eXhq1 I-hydtloxy-2,3,5,6-&&ahq&o-TH-pqwcoLLz~iu-7-catrboxy~~e (21.

1H and13C NMR spectral analysis of some

1H and13C NMR spectral analysis of some necines of toxic pyrrolizidine alkaloids

✍ E. Röder; K. Liu; T. Bourauel 📂 Article 📅 1992 🏛 Springer 🌐 English ⚖ 310 KB

Pyrrolizidine alkaloids necine bases: II

Pyrrolizidine alkaloids necine bases: II. Conformational analysis of free bases

✍ Giordan, Marcelo 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 335 KB 👁 1 views

Molecular mechanics calculations were applied to the Ž . conformational analysis of two diasteroisomers, the pyrrolizidine alkaloids PAs retronecine and heliotridine. The application of reoptimized parameters for H Ž . bonding corrected the tendency of MM3 92 calculations to give unrealistic H иии O