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Volumn 61, Issue 7, 1996, Pages 2283-2292

A novel cycloaddition reaction of α-diazo-γ-amido ketones catalyzed by rhodium(II) acetate. Scope and mechanistic details of the process

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EID: 0000586160     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo952078h     Document Type: Article
Times cited : (20)

References (85)
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    • Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, Chapter 7.3
    • Ziegler, F. E. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Vol. 5, Chapter 7.3.
    • (1991) Comprehensive Organic Synthesis , vol.5
    • Ziegler, F.E.1
  • 6
    • 0003905731 scopus 로고
    • Morrison, J. D., Ed.; Academic Press: Orlando
    • Bartlett, P. A. In Asymmetric Synthesis; Morrison, J. D., Ed.; Academic Press: Orlando, 1984; Vol. 3.
    • (1984) Asymmetric Synthesis , vol.3
    • Bartlett, P.A.1
  • 20
    • 0001216647 scopus 로고
    • Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, Chapter 4.2
    • Curran, D. P In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Vol. 4, Chapter 4.2.
    • (1991) Comprehensive Organic Synthesis , vol.4
    • Curran, D.P.1
  • 68
    • 5244268844 scopus 로고    scopus 로고
    • Calculations were performed with the Mopac program (QCPE 506) using the PM3 Hamiltonian
    • Calculations were performed with the Mopac program (QCPE 506) using the PM3 Hamiltonian.
  • 69
    • 5244372032 scopus 로고    scopus 로고
    • The formation of 25 as a 2:1 mixture of diastereomers might involve racemization via structure 24 or possibly in the preparation of α-diazo ketone 22
    • The formation of 25 as a 2:1 mixture of diastereomers might involve racemization via structure 24 or possibly in the preparation of α-diazo ketone 22.
  • 77
    • 5244358956 scopus 로고
    • For some related 2 + 2 cycloadditions of enamines with acetylenic esters, see: Menachery, M. D.; Carroll, P.; Cava, M. P. Tetrahedron Lett. 1983, 24, 167. Lamm, B.; Aurell, C. J. Acta Chem. Scand. 1982, B36, 435. Lamm, B.; Andersen, L.; Aurell, C. J. Tetrahedron Lett. 1983, 24, 2413.
    • (1983) Tetrahedron Lett. , vol.24 , pp. 167
    • Menachery, M.D.1    Carroll, P.2    Cava, M.P.3
  • 78
    • 5244358956 scopus 로고
    • For some related 2 + 2 cycloadditions of enamines with acetylenic esters, see: Menachery, M. D.; Carroll, P.; Cava, M. P. Tetrahedron Lett. 1983, 24, 167. Lamm, B.; Aurell, C. J. Acta Chem. Scand. 1982, B36, 435. Lamm, B.; Andersen, L.; Aurell, C. J. Tetrahedron Lett. 1983, 24, 2413.
    • (1982) Acta Chem. Scand. , vol.B36 , pp. 435
    • Lamm, B.1    Aurell, C.J.2
  • 79
    • 0343769415 scopus 로고
    • For some related 2 + 2 cycloadditions of enamines with acetylenic esters, see: Menachery, M. D.; Carroll, P.; Cava, M. P. Tetrahedron Lett. 1983, 24, 167. Lamm, B.; Aurell, C. J. Acta Chem. Scand. 1982, B36, 435. Lamm, B.; Andersen, L.; Aurell, C. J. Tetrahedron Lett. 1983, 24, 2413.
    • (1983) Tetrahedron Lett. , vol.24 , pp. 2413
    • Lamm, B.1    Andersen, L.2    Aurell, C.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.