The regioselective S → C and S → N allylic rearrangement of S-allylthioimidate
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference20 articles.
1. A new entry into the synthesis of the nine-membered indole alkaloids related to cleavamine. A stereospecific synthesis of (dl)-4.alpha.-dihydrocleavamine and (dl)-quebrachamine via the thio-Claisen rearrangement
2. Hetero-Cope-Umlagerungen mit dipolaren Zwischenprodukten
3. Stereoselective coupling reaction of thioamides via a dithia-Cope rearrangement
4. 1,4-Addition reaction of organolithium and -magnesium compounds to .alpha.,.beta.-unsaturated thioamides
5. 1,4-Addition reactions of lithium enolates to .alpha.,.beta.-unsaturated thioamides
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