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Volumn 12, Issue 8, 2014, Pages 1245-1249

Organocatalysed synthesis of isoxazolines initiated by a chemoselective oxa-Michael reaction of N-BocNHOH

Author keywords

[No Author keywords available]

Indexed keywords

CHEMOSELECTIVE; ISOXAZOLINES; KETO ESTER; ONE POT;

EID: 84893213040     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c3ob42406e     Document Type: Article
Times cited : (19)

References (47)
  • 15
    • 84857046098 scopus 로고    scopus 로고
    • For selected examples of organocatalysed intramolecular oxa-Michael reactions of hydroxylamines, see
    • H. Pellissier Tetrahedron 2012 68 2197
    • (2012) Tetrahedron , vol.68 , pp. 2197
    • Pellissier, H.1
  • 44
    • 84873354566 scopus 로고    scopus 로고
    • The absolute configuration of isoxazoline 4a was determined through structure similarity after chemical transformation, but the absolute configuration of the other 1,4-dihydroisoxazoles was proposed by analogy due to the similar priority of elution by chiral HPLC
    • L. Hintermann J. Ackerstaff F. Boeck Chem.-Eur. J. 2013 19 2311
    • (2013) Chem.-Eur. J. , vol.19 , pp. 2311
    • Hintermann, L.1    Ackerstaff, J.2    Boeck, F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.