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Volumn 6, Issue 21, 2008, Pages 3967-3969

Access to pyrrolidine imino sugars via tin(II)-mediated aldol reactions of bislactim ethers: Synthesis of 2,5-dideoxy-2,5-imino-d-glucitol

Author keywords

[No Author keywords available]

Indexed keywords

ETHERS; HYDROGEN; HYDROGEN BONDS; ORGANIC COMPOUNDS; SILANES; STEREOSELECTIVITY; SUGAR (SUCROSE); SUGARS; SYNTHESIS (CHEMICAL); TIN; TITANIUM COMPOUNDS;

EID: 58149187121     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b810878a     Document Type: Article
Times cited : (6)

References (32)
  • 28
    • 0000110756 scopus 로고
    • Boat-shaped transition structures with a stabilizing hydrogen bond also account for the anti-selectivity of boron-mediated aldol reactions of β-alkoxy methyl ketones, see: -3361
    • E. P. Lodge C. H. Heathcock J. Am. Chem. Soc. 1987 109 3353 3361
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 3353
    • Lodge, E.P.1    Heathcock, C.H.2
  • 29
    • 39349099300 scopus 로고    scopus 로고
    • Regioselective mesylations of axial hydroxyl groups in diols derived from 2,4-O-benzylidene-d-threose have been previously described, see: -1263
    • R. S. Paton J. M. Goodman J. Org. Chem. 2008 73 1253 1263
    • (2008) J. Org. Chem. , vol.73 , pp. 1253
    • Paton, R.S.1    Goodman, J.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.