메뉴 건너뛰기




Volumn 129, Issue 21, 2007, Pages 6700-6701

Microwave-assisted tandem cross metathesis intramolecular Aza-Michael reaction: An easy entry to cyclic β-amino carbonyl derivatives

Author keywords

[No Author keywords available]

Indexed keywords

CARBONYL DERIVATIVE;

EID: 34249785081     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0709829     Document Type: Article
Times cited : (124)

References (38)
  • 6
    • 1442360753 scopus 로고    scopus 로고
    • Wiley-VCH Verlag Gmbh and Co. KGaA: Weinheim, Germany
    • (a) Grubbs, R. H. In Handbook of Metathesis; Wiley-VCH Verlag Gmbh and Co. KGaA: Weinheim, Germany, 2003; Vol. 1-3.
    • (2003) Handbook of Metathesis , vol.1-3
    • Grubbs, R.H.1
  • 37
    • 34249800711 scopus 로고    scopus 로고
    • The relative stereochemistry of the newly created stereocenter was determined by NOESY experiments over compounds 8a and 9a see Supporting Information
    • The relative stereochemistry of the newly created stereocenter was determined by NOESY experiments over compounds 8a and 9a (see Supporting Information).
  • 38
    • 34249803626 scopus 로고    scopus 로고
    • A solvent study over substrate 7a was performed (with the process under microwave irradiation). The reaction was carried out in DCM, toluene, THF, and acetonitrile. The best results in terms of selectivity and yield were obtained in DCM.
    • A solvent study over substrate 7a was performed (with the process under microwave irradiation). The reaction was carried out in DCM, toluene, THF, and acetonitrile. The best results in terms of selectivity and yield were obtained in DCM.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.