Preparation of Methyl 6 O p Nitrobenzoyl d Glucoside
   
Yazarlar (2)
Prof. Dr. Özlem AKPINAR Tokat Gaziosmanpaşa Üniversitesi, Türkiye
Michael H. Penner Oregon State University, Amerika Birleşik Devletleri
Makale Türü Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale)
Dergi Adı Journal of Carbohydrate Chemistry (Q4)
Dergi ISSN 0732-8303 Wos Dergi Scopus Dergi
Dergi Tarandığı Indeksler SCI
Makale Dili İngilizce Basım Tarihi 01-2008
Cilt / Sayı / Sayfa 27 / 3 / 188–199 DOI 10.1080/07328300802071245
Makale Linki http://www.tandfonline.com/doi/abs/10.1080/07328300802071245
Özet
Methyl 6-O-p-nitrobenzoyl-β-d-glucoside was synthesized by reacting methyl 4,6-O-p-nitrobenzylidine-β-d-glucoside with N-bromosuccinimide (NBS). First, methyl β-d-glucoside was converted into methyl 4,6-O-p-nitrobenzylidine-β-d-glucoside with p-nitrobenzaldehyde. Later, methyl 4,6-O-p-nitrobenzylidine-β-d-glucoside was opened oxidatively with NBS to give methyl 6-O-p-nitrobenzoyl-β-d-glucoside. Copyright © Taylor & Francis Group, LLC.
Anahtar Kelimeler
Cyclic acetals | NBS | Nitrobenzoyl | Nonreducing end | Oxidation
Science Direct
BM Sürdürülebilir Kalkınma Amaçları
Atıf Sayıları
Web of Science 1
Preparation of Methyl 6 O p Nitrobenzoyl d Glucoside

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