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Volumn 2, Issue 7, 1996, Pages 805-811

Enantioselective synthesis of highly functionalized 4-piperidones by the asymmetric imino-Diels-Alder reaction of chiral 2-amino-1,3-butadienes

Author keywords

Asymmetric Diels Alder reactions; Butadienes; Diels Alder reactions; Piperidones

Indexed keywords

ABSOLUTE CONFIGURATION; DIELS-ALDER REACTION; ENANTIOMERIC EXCESS; ENANTIOSELECTIVE SYNTHESIS; FUNCTIONALIZED; IMINO-DIELS-ALDER; PIPERIDONES;

EID: 0000045250     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.19960020712     Document Type: Article
Times cited : (43)

References (44)
  • 30
    • 84891287564 scopus 로고    scopus 로고
    • note
    • 4J(H 3,H 5) = 1.3 Hz] is observed due to the planar W geometry.
  • 33
    • 84891288667 scopus 로고    scopus 로고
    • Serena Software: P. O. Box 3076, Bloomington, IN 47402-3076
    • MMX force field. PCMODEL-PI (v 4.0), Serena Software: P. O. Box 3076, Bloomington, IN 47402-3076.
    • MMX Force Field. PCMODEL-PI (v 4.0)
  • 34
    • 84891280959 scopus 로고    scopus 로고
    • note
    • The strain energy differences, rotamer distributions, and especially dihedral angles O4-C4-C7-O7 found for the rotamers of compound 13 are of great interest for CD analysis.
  • 35
    • 84891309956 scopus 로고    scopus 로고
    • note
    • -1 and HPLC grade n-hexane/EtOAc (85:15) solvent system.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.