Thioamidoalkylation of 1,3-dicarbonyl compounds, enol silyl ethers, and enamines
SYNTHESIS-STUTTGART, sa.11, ss.1655-1662, 2007 (SCI-Expanded, Scopus)
- Yayın Türü: Makale / Tam Makale
- Basım Tarihi: 2007
- Doi Numarası: 10.1055/s-2007-966064
- Dergi Adı: SYNTHESIS-STUTTGART
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Index Chemicus (IC), Current Chemical Reactions (CCR)
- Sayfa Sayıları: ss.1655-1662
- Anahtar Kelimeler: thioamides, N-(alpha-thioamidoalkyl)benzotriazoles, thioamidoalkylation, 1,3-dicarbonyl compounds, enol silyl ethers, enamines, ALPHA-THIOAMIDOALKYLATION, UNSATURATED-COMPOUNDS, FUNGISTATIC ACTIVITY, HETEROCYCLES, THIOAMIDES, BENZOTRIAZOLE, THIONATION, AMIDES, 2,4-DIHYDROXYTHIOBENZANILIDES, 6H-1,3,5-OXATHIAZINES
- Anadolu Üniversitesi Adresli: Evet
Özet
Novel syntheses of beta-thioamido ketones via thioamidoalkylations of malonates, beta-keto esters, beta-diketones, enol silyl ethers, and enamines with N-(alpha-thioamidoalkyl)benzotriazoles are described.