✦ LIBER ✦

The incorporation of [5,6-13C2]Nicotinic acid into the tobacco alkaloids examined by the use of 13C nuclear magnetic resonance

✍ Scribed by Edward Leete

Book ID: 107873690
Publisher: Elsevier Science
Year: 1977
Tongue: English
Weight: 817 KB
Volume: 6
Category: Article
ISSN: 0045-2068
DOI: 10.1016/0045-2068(77)90029-3

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Biosynthesis of the isoquinuclidine moie

Biosynthesis of the isoquinuclidine moiety of dioscorine. Incorporation of [5,6-13C2]nicotinic acid established by means of carbon-13 nuclear magnetic resonance

✍ Leete, Edward 📂 Article 📅 1977 🏛 American Chemical Society 🌐 English ⚖ 367 KB

Incorporation of [2-14C]- and [6-14C]nic

Incorporation of [2-14C]- and [6-14C]nicotinic acid into the tobacco alkaloids. Biosynthesis of anatabine and .alpha.,.beta.-dipyridyl

✍ Leete, Edward; Slattery, Sheila A. 📂 Article 📅 1976 🏛 American Chemical Society 🌐 English ⚖ 625 KB

Aberrant syntheses in higher plants. 4.

Aberrant syntheses in higher plants. 4. Aberrant biosynthesis of 5-fluoroanabasine from 5-fluoro[5,6-14C,13C2]nicotinic acid, established by means of carbon-13 nuclear magnetic resonance

✍ Leete, Edward 📂 Article 📅 1979 🏛 American Chemical Society 🌐 English ⚖ 514 KB

The 13C nuclear magnetic resonance spect

The 13C nuclear magnetic resonance spectra of some 2-, 6-, and 2,6-substituted purines

✍ Martha C Thorpe; W.C Coburn Jr.; John A Montgomery 📂 Article 📅 1974 🏛 Elsevier Science ⚖ 971 KB

The incorporation of ornithine-[2,3-13C2

The incorporation of ornithine-[2,3-13C2] into nicotine and nornicotine established by NMR

✍ Edward Leete; Ming-Li Yu 📂 Article 📅 1980 🏛 Elsevier Science 🌐 English ⚖ 425 KB

Biosynthesis of secalonic acid A. The pa

Biosynthesis of secalonic acid A. The pathway indicated by a 13C nuclear magnetic resonance study of acetate incorporation

✍ Itsuo Kurobane; Leo C. Vining; A.Gavin McInnes; John A. Walter; Jeffrey L.C. Wri 📂 Article 📅 1978 🏛 Elsevier Science 🌐 French ⚖ 195 KB

Studies on ergochrome biosynthesis with "C-labelled acetate'\*' and 14C-and 'H-labelled emodin (2)2,3 are consistent with the pathway octaketide (1) + anthraquinone (2) + benzophenone carboxylic ester (3) + tetrahydroxanthone (4) + ergochrome (e.g. !a-4a), but do not exclude dimerization of ,2 or so