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The generation of 2,3-dihydro-2,3-bis-(methylene)thiophenes from 4,6-dihydrothieno[3,4-b]thiophene 5,5-dioxides

✍ Scribed by A.P.A. Crew; G. Jenkins; R.C. Storr; M. Yelland


Book ID
104222109
Publisher
Elsevier Science
Year
1990
Tongue
French
Weight
219 KB
Volume
31
Category
Article
ISSN
0040-4039

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✦ Synopsis


On heating in sulpholane 4,6-dihydrothieno[3,4-blthiophene 5,5-dioxides give 2,3dihydro-2,3-bis(methylene)thiophenes which can be intercepted in Diels-Alder reactions. Sulphur dioxide is a very efficient trap for these thiophene xylylenes giving the cyclic sulphones by cheletropic addition.


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Synthesis of 2-amino-4,5-dihydro-3-metha
✍ Kenji Yamagata; Fumi Okabe; Hiroshi Maruoka; Yoshinobu Tagawa 📂 Article 📅 2005 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 79 KB

## Abstract 2‐Amino‐4,5‐dihydro‐3‐methanesulfonylfurans **7** and 2‐amino‐4,5‐dihydro‐3‐methanesulfonylthiophenes **8** were prepared by deamidation of tetrahydro‐2‐imino‐3‐methanesulfonyl‐3‐furancarboxamides **3** and of tetrahydro‐2‐imino‐3‐methanesulfonyl‐3‐thiophenecarboxamides **4** with bases