2-O-Benzylation in D-Gluconamide Derivative Under Basic Conditions with Complete Retention of Stereo-Integrity: Convenient Access to 2-O-benzyl-3,4:5,6- di-O-isopropylidene-D-glucitol and other Differently Protected D-glucitol Derivatives

Autor:	Indrapal Singh Aidhen, B. N. Manjunath, Kommidi Harikrishna, Babu Varghese
Rok vydání:	2009
Předmět:	Chemistry Stereochemistry Organic Chemistry D-glucitol Biochemistry D-gluconamide
Zdroj:	Journal of Carbohydrate Chemistry. 28:264-277
ISSN:	1532-2327 0732-8303
DOI:	10.1080/07328300902979503
Popis:	A new and convenient synthesis of 2-O-benzyl-3, 4: 5, 6-di-O- isopropylidene-D-glucitol has been accomplished and has been generalized with the syntheses of differently protected D-glucitols at C-2 position. In the course of our new route to the differently protected D-glucitols at C-2 position, a new D-gluco configured building block, 1-morpholino-(3, 4: 5, 6-di-O-isopropylidene)-D-gluconamide has been achieved.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fc9cff5be5f3cf60f0b800d2f051a0a https://doi.org/10.1080/07328300902979503 Zobrazit plný text záznamu Plný text ve formátu PDF Plný text ve formátu HTML
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