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Volumn 17, Issue 21, 2011, Pages 5881-5889

An easy and versatile approach for the regioselective De-O-benzylation of protected sugars based on the I2/Et3SiH combined system

Author keywords

benzyl ethers; carbohydrates; protecting groups; regioselectivity

Indexed keywords

BENZYL ETHERS; BUILDING BLOCKES; CHIRAL COMPOUNDS; COMBINED SYSTEM; DEPROTECTION; ELECTRONWITHDRAWING; ESTER GROUPS; FULLY PROTECTED; GLYCOSYL DONORS; IN-SITU; LEWIS X; LOW TEMPERATURES; MONO- AND DISACCHARIDES; ONE-POT SYNTHESIS; PROTECTING GROUP; PROTECTING GROUPS; REGIO-SELECTIVE; STERIC EFFECT;

EID: 79955784737     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201003332     Document Type: Article
Times cited : (40)

References (94)
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    • note
    • 3SiH at low temperature.
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    • note
    • In a reasonable hypothesis, the 5-OH furanoside intermediate could be involved in an intramolecular trans-acetalation with expulsion of allyl alcohol and generation of a 1,5-anhydro bicyclo structure.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.