𝔖 Bobbio Scriptorium
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Specifically deuterated and tritiated auxins

✍ Scribed by L.Lee Melhado; Cedric J. Pearce; Marc d'Alarcao; Nelson J. Leonard


Book ID
103332788
Publisher
Elsevier Science
Year
1980
Tongue
English
Weight
913 KB
Volume
21
Category
Article
ISSN
0031-9422

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πŸ“œ SIMILAR VOLUMES


Specifically tritiated arene oxides
✍ Haruhiko Yagi; Patrick Dansette; Donald M. Jerina πŸ“‚ Article πŸ“… 1976 πŸ› John Wiley and Sons 🌐 French βš– 272 KB

## Abstract Convenient methods have been developed for the preparation of specifically tritiated arene oxides. K‐Region arene oxides of phenanthene, benzo[a]anthracene and benzo[a]pyrene were prepared from triatiated cis dihydrodiols via the methoxydioxolane route and the non‐K‐region arene oxides,

Synthesis of deuterated and tritiated ap
✍ Larry J. Powers; Preston H. Dorsett πŸ“‚ Article πŸ“… 1980 πŸ› John Wiley and Sons 🌐 French βš– 203 KB

## Abstract Apogossypol with deuterium or tritium in the 8 and 8β€² positions can be synthesized by the base catalyzed deformylation of gossypol. The position of the labeling is established by the pmr spectrum of the material derived from the reaction of deuterium oxide and sodium deuteroxide. The sp

Synthesis of deuterated and tritiated go
✍ Robert D. Stipanovic; Howard J. Williams; David P. Muehleisen; F. W. Plapp Jr. πŸ“‚ Article πŸ“… 1987 πŸ› John Wiley and Sons 🌐 French βš– 126 KB
Synthesis of specifically-deuterated pro
✍ Yvan Boulanger; Leonard C. Leitcht πŸ“‚ Article πŸ“… 1981 πŸ› John Wiley and Sons 🌐 French βš– 290 KB

## Abstract Local anesthetics procaine and tetracaine have been specifically‐deuterated in two and three positions, respectively, for use in deuterium nuclear magnetic resonance experiments. The experimental procedure is either new or an adaptation of early synthetic methods.

Synthesis of deuterated and tritiated de
✍ Terrence R. Burke Jr.; Lance R. Pohl πŸ“‚ Article πŸ“… 1981 πŸ› John Wiley and Sons 🌐 French βš– 296 KB

## Abstract Specifically deuterated derivatives of the inhalation anesthetic enflurane [2‐chloro‐1‐(difluoromethoxy)‐1,1,2‐trifluoroethane] have been synthesized by a facile base catalyzed exchange. Tritiated enflurane has also been synthesized by this procedure.