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Volumn 3, Issue 7, 2013, Pages 2404-2411

A reagent based DOS strategy via Evans chiral auxiliary: Highly stereoselective Michael reaction towards optically active quinolizidinones, piperidinones and pyrrolidinones

Author keywords

[No Author keywords available]

Indexed keywords

ANTIMICROBIAL PROPERTY; CHIRAL AUXILIARIES; DIVERSITY-ORIENTED SYNTHESIS; IN-SILICO; MICHAEL ADDUCTS; MICHAEL REACTIONS; NITROGEN HETEROCYCLES; OPTICALLY ACTIVE; OXAZOLINES; PIPERIDINONES; POLAR SURFACE AREAS; SHAPE SPACE; STEREO-SELECTIVE;

EID: 84872698221     PISSN: None     EISSN: 20462069     Source Type: Journal    
DOI: 10.1039/c2ra22115b     Document Type: Article
Times cited : (13)

References (54)
  • 51
    • 45849102419 scopus 로고    scopus 로고
    • Please refer to the NOE in the experimental section GVK Bioscience proprietary database Stable 3D structures of all compounds were used to calculate their physicochemical properties, such as molecular weight, number of hydrogen-bond donors (HBD), number of hydrogen bond acceptors (HBA), ALogP, LogD and polar surface area (PSA), these values were calculated by using Discovery Studio 3.1 (Accelrys Inc.)
    • P. S. Hynes P. A. Stupple D. J. Dixon Org. Lett. 2008 10 7 1389 1391
    • (2008) Org. Lett. , vol.10 , Issue.7 , pp. 1389-1391
    • Hynes, P.S.1    Stupple, P.A.2    Dixon, D.J.3
  • 53
    • 84872696194 scopus 로고    scopus 로고
    • GVKBio proprietary software
    • GVKBio proprietary software


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.