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New Synthetic Route to Di- and Trisubstituted Epoxides

✍ Scribed by Dr. Willy Dumont; Prof. Dr. Alain Krief

Publisher
John Wiley and Sons
Year
1975
Tongue
English
Weight
218 KB
Volume
14
Category
Article
ISSN
0044-8249

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πŸ“œ SIMILAR VOLUMES

A New Route to Epoxides
A New Route to Epoxides
✍ Dipl.-Chem. D. Van Ende; Dr. Willy Dumont; Prof. Dr. Alain Krief πŸ“‚ Article πŸ“… 1975 πŸ› John Wiley and Sons 🌐 English βš– 342 KB πŸ‘ 2 views
A new route to di- and trisubstituted ol
A new route to di- and trisubstituted olefins via lithium trialkylalkynylborates
✍ John Hooz; Richard Mortimer πŸ“‚ Article πŸ“… 1976 πŸ› Elsevier Science 🌐 French βš– 160 KB

Recclved 111 USA 16 January 1976; received in UK for publfcetlon 5 Febraq ~976) The rearrangement of trlalkylalkynylborate salts (I) has been induced by a variety of electrophlles, and the stereochemlcal outcome 1s a complex function of several factors, lncludlng the nature of the electrophlle, the

A New Synthetic Route to Aminothiazolino
A New Synthetic Route to Aminothiazolinones.
✍ M. Kidwai; A. D. Mishra πŸ“‚ Article πŸ“… 2004 πŸ› John Wiley and Sons βš– 103 KB πŸ‘ 2 views

## Abstract For Abstract see ChemInform Abstract in Full Text.

A New Synthetic Route to (Β±)-Perhydrohis
A New Synthetic Route to (Β±)-Perhydrohistrionicotoxin
✍ E. J. Corey; Martin Petrzilka; Yoichiro Ueda πŸ“‚ Article πŸ“… 1977 πŸ› John Wiley and Sons 🌐 German βš– 604 KB

## Abstract Starting from ethyl 2‐cyclohexen‐1‐carboxylate (**3**) the total synthesis of the perhydrohistrionicotoxin intermediate **23** was achieved in 25% overall‐yield. The two key steps involve a positionally specific addition of HOBr to the oxime‐olefin **7** and the alkylation of bromooxime