Preparation of new mono- and bis-amide derivatives of L-isoleucine via amidation of carboxyl and amino groups
Yazarlar (5)
Murat Sunkur Batman Üniversitesi, Türkiye
Sara Aydın Batman Üniversitesi, Türkiye
Prof. Dr. Tarık Aral Batman Üniversitesi, Türkiye
Doç. Dr. Beşir Dağ Batman Üniversitesi, Türkiye
Prof. Dr. Ramazan ERENLER Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Makale Türü Açık Erişim Özgün Makale (ESCI dergilerinde yayınlanan tam makale)
Dergi Adı Organic Communications
Dergi ISSN 1307-6175 Dergi Bilgileri (2021)
Dergi Tarandığı Indeksler TR DİZİN
Makale Dili İngilizce Basım Tarihi 07-2021
Kabul Tarihi – Yayınlanma Tarihi 19-09-2021
Cilt / Sayı / Sayfa 14 / 3 / 294–299 DOI 10.25135/acg.oc.112.21.07.2139
Makale Linki http://dx.doi.org/10.25135/acg.oc.112.21.07.2139
UAK Araştırma Alanları
Organik Kimya
Özet
N, N′-Dicyclohexylcarbodiimide and hydroxybenzotriazole mediated amination of free COOH group of N-tert-butyloxyoxycarbonyl-L-isoleucine 1 with three aromatic amines gave the corresponding amides 2a-c. Deprotection of N-tert-butyloxyoxycarbonyl groups of 2a-c with AcOH yielded the related amine derivatives 3a-c. The amidation of the free NH2 groups of (3a-c) with phthaloyl dichloride yielded the bis-amide products 4a-c. The synthesized compounds were purified by crystallization and their structures were elucidated by spectroscopic methods such as 1H-HMR, 13C-NMR, FTIR, and micro analysis.
Anahtar Kelimeler
Amides | coupling reaction | heterocyclic | N-boc-deprotection | spectroscopy | tetraamides
BM Sürdürülebilir Kalkınma Amaçları
Atıf Sayıları
Web of Science 3
Scopus 4
Google Scholar 7
TR Dizin 2
Preparation of new mono- and bis-amide derivatives of L-isoleucine via amidation of carboxyl and amino groups