Synthesis of the four possible stereoisomeric 5′-nor carbocyclic nucleosides from one common enantiomerically pure starting material

Autor:	Natalja Dyatkina, Fritz Theil, Martin von Janta-Lipinski, Burkhard Costisella
Rok vydání:	1994
Předmět:	Allylic rearrangement chemistry.chemical_compound Chemistry Stereochemistry Organic Chemistry Drug Discovery Diol Organic chemistry Biochemistry
Zdroj:	Tetrahedron Letters. 35:1961-1964
ISSN:	0040-4039
DOI:	10.1016/s0040-4039(00)73022-x
Popis:	A flexible synthesis of the four stereoisomeric enantiomerically pure 5′-nor carbocyclic nucleosides 2b, ent-2b, 3b, and ent-3b starting from the common enantiomerically pure allylic monoacetate 1 has been developed.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::534f5c876be98b2831c0515e6bc76346 https://doi.org/10.1016/s0040-4039(00)73022-x Zobrazit plný text záznamu