Amination/annulation of chlorobutenones with chiral amine compounds: synthesis of 1,2,4-trisubstituted pyrroles
TETRAHEDRON-ASYMMETRY, cilt.16, sa.19, ss.3170-3175, 2005 (SCI-Expanded, Scopus)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 16 Sayı: 19
- Basım Tarihi: 2005
- Doi Numarası: 10.1016/j.tetasy.2005.08.033
- Dergi Adı: TETRAHEDRON-ASYMMETRY
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Sayfa Sayıları: ss.3170-3175
- Orta Doğu Teknik Üniversitesi Adresli: Evet
Özet
A series of 1,2,4-trisubstituted pyrroles have been synthesized in 83-96% yields on treatment of chiral primary amines, amino alcohols and esters of alpha-amino acids with different chlorobutenones in benzene-triethylamine. The conversions proceed without racemization. (c) 2005 Elsevier Ltd. All rights reserved.