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The regioselective S → C and S → N allylic rearrangement of S-allylthioimidate

✍ Scribed by Y. Tamaru; M. Kagotani; Z. Yoshida

Publisher
Elsevier Science
Year
1981
Tongue
French
Weight
261 KB
Volume
22
Category
Article
ISSN
0040-4039

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✦ Synopsis

The regioseZective S + C and S + N allyLie rearrangements of S-allylthioimidates are realized by thermoZysis (160~2OO'C) or paZladiwn (II) cataZysis cl%10 mol% in refluxing THFI, respectiveZy.

📜 SIMILAR VOLUMES

ChemInform Abstract: Allylic Dithioaceta
ChemInform Abstract: Allylic Dithioacetals as a Propene-1,3-Zwitterion Synthon. Regioselective Conversion of C—S Bonds in Allylic Dithioacetals into C—C Bonds.
✍ Chao-Cheng Chiang; Tien-Yau Luh 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB 👁 2 views

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