Electrophilic glycosidation employing 3,5-O-(di-tert-butylsilylene)-erythro-furanoid glycal leads to exclusive formation of the β-anomer: synthesis of 2′-deoxynucleosides and its 1′-branched analogues-Reference-Cited by-同舟云学术

Electrophilic glycosidation employing 3,5-O-(di-tert-butylsilylene)-erythro-furanoid glycal leads to exclusive formation of the β-anomer: synthesis of 2′-deoxynucleosides and its 1′-branched analogues

Published:2010-06 Issue:25 Volume:66 Page:4587-4600
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Haraguchi Kazuhiro,Konno Kiju,Yamada Kaori,Kitagawa Yasuyuki,Nakamura Kazuo T.,Tanaka Hiromichi

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference51 articles.

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2. An efficient and highly stereoselective synthesis of nucleoside derivatives from furanoid 1,2-diols

3. Synthesis of 2′-deoxy-2′-phenylselenenyl-furanosyl nucleosides from glycals using electrophilic selenium reagents. Conversion into 2′-deoxynucleosides

4. Stereoselective Synthesis of 2‘,3‘-Dideoxynucleosides by Addition of Selenium Electrophiles to Glycals. A Formal Synthesis of D4T from 2-Deoxyribose

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