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Synthesis of 2-thiabicyclo[3.2.0]hept-3-enes by reaction of acetylene with sodium sulfide

✍ Scribed by B. A. Trofimov; G. A. Kalabin; V. V. Kryuchkov; V. V. Keiko; S. V. Amosova; V. M. Bzhezovskii; V. K. Voronov; D. F. Kushnarev; V. Yu. Vitkovskii; L. I. Lavlinskaya; V. A. Pestunovich


Book ID
112330022
Publisher
Springer US
Year
1976
Tongue
English
Weight
303 KB
Volume
12
Category
Article
ISSN
0009-3122

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πŸ“œ SIMILAR VOLUMES


1H and 13C NMR spectra of new 2-thiabicy
✍ G. A. Kalabin; B. A. Trofimov πŸ“‚ Article πŸ“… 1978 πŸ› John Wiley and Sons 🌐 English βš– 358 KB

Three new compounds, one with the mo~ecular formula c6&s and hvo COmspOnding to GHloS have been isolated together with the main product, divinyl sulphide, from the reaction products of acetylene with sodium sulphide. Structure determination through 'H and 13C NMR with selective "C4'H) decoupling, sh

Captodative dienes in cycloaddition cond
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m Aminobicyclo (3.2.0) heptenones and aminonorbornenones were obtained from methylacrylate or acrylonitrile and captodative dienes. They result from respectively (2+2) and (4+2) cycloadditions.