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Volumn , Issue 7, 2006, Pages 1039-1042

Stereoselective ring-opening of N-tert-butanesulfinylaziridines: Access to acetylenic α-amino alcohols

Author keywords

Amino alcohols; Asymmetric synthesis; Aziridines; Diastereoselectivity; Regioselectivity

Indexed keywords

ALPHA AMINO ALCOHOL; AMINOALCOHOL; AZIRIDINE DERIVATIVE; N TERT BUTANESULFINYLAZIRIDINE DERIVATIVE; OXAZOLIDINONE DERIVATIVE; UNCLASSIFIED DRUG; WATER;

EID: 33646597768     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-939063     Document Type: Article
Times cited : (22)

References (53)
  • 1
    • 1542375289 scopus 로고    scopus 로고
    • For a recent review on the ring-opening reaction of aziridines by nucleophiles, see: Hu, X. E. Tetrahedron 2004, 60, 2701.
    • (2004) Tetrahedron , vol.60 , pp. 2701
    • Hu, X.E.1
  • 2
    • 28244452919 scopus 로고    scopus 로고
    • For some very recent syntheses involving ring-opening of aziridines, see: (a) Li, P.; Evans, C. D.; Joullié, M. M. Org. Lett. 2005, 7, 5325.
    • (2005) Org. Lett. , vol.7 , pp. 5325
    • Li, P.1    Evans, C.D.2    Joullié, M.M.3
  • 15
    • 0242558390 scopus 로고    scopus 로고
    • For some selected recent examples, see: (a) Satoh, T.; Fukuda, Y. Tetrahedron 2003, 59, 9803.
    • (2003) Tetrahedron , vol.59 , pp. 9803
    • Satoh, T.1    Fukuda, Y.2
  • 50
    • 33646543650 scopus 로고    scopus 로고
    • note
    • 2, 1:9) to first give regioisomers 5a-g and then the corresponding diastereo- and enantiomerically pure acetylenic α-amino alcohols 4a-g.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.