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Volumn 69, Issue 12, 2004, Pages 4192-4202

N-vinyl-2-oxazolidinones: Efficient chiral dienophiles for the [4 + 2]-based de novo synthesis of new N-2-deoxyglycosides

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; INORGANIC ACIDS; ISOMERS; KETONES; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

EID: 2942615070     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo040102y     Document Type: Article
Times cited : (45)

References (57)
  • 41
    • 0142089019 scopus 로고    scopus 로고
    • Gaulon, C.; Dhal, R.; Dujardin, G. Synthesis 2003, 2269. The N-vinyl-2-oxazolidinone 1f17a was prepared according this procedure in 85% overall yield.
    • (2003) Synthesis , pp. 2269
    • Gaulon, C.1    Dhal, R.2    Dujardin, G.3
  • 44
    • 2942613158 scopus 로고    scopus 로고
    • note
    • Further experiments using SnC14 as an alternative Lewis acid confirmed our previous observations in achiral series: reaction proceeded at low temperature with low or without diastereoselectivities.
  • 49
    • 0025113441 scopus 로고
    • For efficient uses of chiral N-vinyloxazolidinones (i) in asymmetric Pd-promoted carboacylations and alkylations, see: (a) Montgomery, J.; Wieber, G. M.; Hegedus, L. S. J. Am. Chem. Soc. 1990, 112, 6255.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 6255
    • Montgomery, J.1    Wieber, G.M.2    Hegedus, L.S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.