메뉴 건너뛰기




Volumn 48, Issue 1, 2012, Pages 179-190

Fused aziridines as sources of azomethine ylides

Author keywords

1,3 dipolar cycloaddition; aziridines; azomethine ylides; heterocycles

Indexed keywords


EID: 84861231344     PISSN: 00093122     EISSN: 15738353     Source Type: Journal    
DOI: 10.1007/s10593-012-0981-7     Document Type: Article
Times cited : (14)

References (40)
  • 2
    • 23044431676 scopus 로고    scopus 로고
    • Intramolecular dipolar cycloaddition reactions of azomethine ylides
    • DOI 10.1021/cr040004c
    • I Coldham R Hufton 2005 Chem. Rev. 105 2765 10.1021/cr040004c 1:CAS:528:DC%2BD2MXlsFKrtr8%3D (Pubitemid 41055330)
    • (2005) Chemical Reviews , vol.105 , Issue.7 , pp. 2765-2809
    • Coldham, I.1    Hufton, R.2
  • 4
    • 0004026247 scopus 로고    scopus 로고
    • J.S. Clark (eds). Oxford University Press Oxford
    • J. S. Clark (editor), Nitrogen, Oxygen and Sulfur Ylide Chemistry, Oxford University Press, Oxford (2002).
    • (2002) Nitrogen, Oxygen and Sulfur Ylide Chemistry
  • 10
    • 2742588167 scopus 로고
    • 10.1021/ja01076a095 1:CAS:528:DyaF2MXhsV2iuw%3D%3D
    • E Ullman WA Henderson Jr 1964 J. Am. Chem. Soc. 86 5050 10.1021/ja01076a095 1:CAS:528:DyaF2MXhsV2iuw%3D%3D
    • (1964) J. Am. Chem. Soc. , vol.86 , pp. 5050
    • Ullman, E.1    Henderson Jr., W.A.2
  • 12
    • 0001567675 scopus 로고
    • 10.1021/jo00838a037 1:CAS:528:DyaF1MXlslOksw%3D%3D
    • HW Heine RP Henzel 1969 J. Org. Chem 34 171 10.1021/jo00838a037 1:CAS:528:DyaF1MXlslOksw%3D%3D
    • (1969) J. Org. Chem , vol.34 , pp. 171
    • Heine, H.W.1    Henzel, R.P.2
  • 14
    • 0347456731 scopus 로고
    • 10.1021/ja00769a024 1:CAS:528:DyaE38XkvVynt7g%3D
    • A Padwa L Gehrlein 1972 J. Am. Chem. Soc. 94 4933 10.1021/ja00769a024 1:CAS:528:DyaE38XkvVynt7g%3D
    • (1972) J. Am. Chem. Soc. , vol.94 , pp. 4933
    • Padwa, A.1    Gehrlein, L.2
  • 21
    • 0032514580 scopus 로고    scopus 로고
    • The photochemistry of α-azidocinnamates - A reinvestigation
    • DOI 10.1016/S0040-4020(98)00537-7, PII S0040402098005377
    • O Meth-Cohn NJR Williams A MacKinnon JAK Howard 1998 Tetrahedron 54 9837 10.1016/S0040-4020(98)00537-7 1:CAS:528:DyaK1cXltFehsb4%3D (Pubitemid 28343412)
    • (1998) Tetrahedron , vol.54 , Issue.33 , pp. 9837-9848
    • Meth-Cohn, O.1    Williams, N.J.R.2    MacKinnon, A.3    Howard, J.A.K.4
  • 24
  • 25
    • 0024988763 scopus 로고
    • Microbial oxidation of chloroaromatics in the enantiodivergent synthesis of pyrrolizidine alkaloids: Trihydroxyheliotridanes
    • DOI 10.1021/jo00302a037
    • T Hudlicky H Luna JD Price F Rulin 1990 J. Org. Chem. 55 4683 10.1021/jo00302a037 1:CAS:528:DyaK3cXksF2lt70%3D (Pubitemid 20274272)
    • (1990) Journal of Organic Chemistry , vol.55 , Issue.15 , pp. 4683-4687
    • Hudlicky, T.1    Luna, H.2    Price, J.D.3    Rulin, F.4
  • 26
    • 0035858655 scopus 로고    scopus 로고
    • Ring transformations of 2,3-dihydroisoxazoles via azomethine ylides - Formation of annulated 5- and 7-membered N-heterocycles
    • DOI 10.1016/S0040-4020(01)00322-2, PII S0040402001003222
    • W Friebolin W Eberbach 2001 Tetrahedron 57 4349 10.1016/S0040-4020(01) 00322-2 1:CAS:528:DC%2BD3MXjtlWjt70%3D (Pubitemid 32441629)
    • (2001) Tetrahedron , vol.57 , Issue.20 , pp. 4349-4358
    • Friebolin, W.1    Eberbach, W.2
  • 27
    • 0342320201 scopus 로고
    • 10.1021/jo00390a002 1:CAS:528:DyaL2sXkvFKmtr8%3D
    • AG Schultz RR Staib KK Eng 1987 J. Org. Chem. 52 2968 10.1021/jo00390a002 1:CAS:528:DyaL2sXkvFKmtr8%3D
    • (1987) J. Org. Chem. , vol.52 , pp. 2968
    • Schultz, A.G.1    Staib, R.R.2    Eng, K.K.3
  • 29
    • 0342513381 scopus 로고
    • 10.1021/jo00809a020 1:CAS:528:DyaE3MXktlCrs7s%3D
    • JW Lown K Matsumoto 1971 J. Org. Chem. 36 1405 10.1021/jo00809a020 1:CAS:528:DyaE3MXktlCrs7s%3D
    • (1971) J. Org. Chem. , vol.36 , pp. 1405
    • Lown, J.W.1    Matsumoto, K.2
  • 34
    • 84943951453 scopus 로고
    • 10.1248/cpb.17.2461 1:CAS:528:DyaE3cXnvVOrsg%3D%3D
    • S Oida E Ohki 1969 Chem. Pharm. Bull 17 2461 10.1248/cpb.17.2461 1:CAS:528:DyaE3cXnvVOrsg%3D%3D
    • (1969) Chem. Pharm. Bull , vol.17 , pp. 2461
    • Oida, S.1    Ohki, E.2
  • 36
    • 0001529145 scopus 로고
    • 10.1016/0040-4039(88)85283-3 1:CAS:528:DyaL1MXitFeitL8%3D
    • P Garner K Sunitha T Shanthilal 1988 Tetrahedron Lett. 29 3525 10.1016/0040-4039(88)85283-3 1:CAS:528:DyaL1MXitFeitL8%3D
    • (1988) Tetrahedron Lett. , vol.29 , pp. 3525
    • Garner, P.1    Sunitha, K.2    Shanthilal, T.3
  • 37
    • 0024512040 scopus 로고
    • An asymmetric approach to naphthyridinomycin and quinocarcin via a remarkably selective intramolecular 1,3-dipolar cycloaddition reaction
    • DOI 10.1021/jo00270a008
    • P Garner K Sunitha W-B Ho WJ Youngs VO Kennedy A Djebli 1989 J. Org. Chem. 54 2041 10.1021/jo00270a008 1:CAS:528:DyaL1MXitFant74%3D (Pubitemid 19119272)
    • (1989) Journal of Organic Chemistry , vol.54 , Issue.9 , pp. 2041-2042
    • Garner, P.1    Sunitha, K.2    Ho, W.-B.3    Youngs, W.J.4    Kennedy, V.O.5    Djebli, A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.