메뉴 건너뛰기




Volumn 105, Issue 7, 2005, Pages 2829-2871

Some typical advances in the synthetic applications of allenes

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; APPLICATIONS; CATALYSIS; CHEMICAL BONDS; FREE RADICAL REACTIONS; IRRADIATION; MOLECULAR DYNAMICS; ORGANOMETALLICS; OXIDATION; UNSATURATED COMPOUNDS;

EID: 22944485617     PISSN: 00092665     EISSN: None     Source Type: Journal    
DOI: 10.1021/cr020024j     Document Type: Review
Times cited : (1239)

References (351)
  • 3
    • 0004175549 scopus 로고
    • Schuster, H. F., Coppola, G. M., Eds.; John Wiley & Sons: New York
    • (a)Allenes in Organic Synthesis; Schuster, H. F., Coppola, G. M., Eds.; John Wiley & Sons: New York, 1984.
    • (1984) Allenes in Organic Synthesis
  • 5
    • 4544320494 scopus 로고    scopus 로고
    • Krause, N., Hashmi, A. S. K., Eds.; Wiley-VCH: Weinheim
    • (c) Modern Allene Chemistry; Krause, N., Hashmi, A. S. K., Eds.; Wiley-VCH: Weinheim, 2004.
    • (2004) Modern Allene Chemistry
  • 11
  • 19
    • 22944443077 scopus 로고    scopus 로고
    • Pd-Catalyzed two- or three-component cyclization of functionalized allenes
    • Tsuji, J., Ed.; Springer-Verlag: Heidelberg
    • Ma, S. Pd-Catalyzed two- or three-component cyclization of functionalized allenes. In Topics in Organometallic Chemistry; Tsuji, J., Ed.; Springer-Verlag: Heidelberg, 2005; pp 183-210.
    • (2005) Topics in Organometallic Chemistry , pp. 183-210
    • Ma, S.1
  • 24
    • 22944471259 scopus 로고    scopus 로고
    • For recent synthetic applications, see: 753 and references therein. For [2+2] cycloaddition of allenes by Pasto et al., see ref 4m
    • For recent synthetic applications, see: Morimoto, T.; Horiguchi, T.; Yamada, K.; Tsutsumi, K.; Kurosawa, H.; Kakiuchi, K. Synthesis 2004, 753 and references therein. For [2+2] cycloaddition of allenes by Pasto et al., see ref 4m.
    • (2004) Synthesis
    • Morimoto, T.1    Horiguchi, T.2    Yamada, K.3    Tsutsumi, K.4    Kurosawa, H.5    Kakiuchi, K.6
  • 43
    • 0001664642 scopus 로고
    • For a review, see
    • (d) For a review, see: Toda, F.; Garratt, P. Chem. Rev. 1992, 92, 1685.
    • (1992) Chem. Rev. , vol.92 , pp. 1685
    • Toda, F.1    Garratt, P.2
  • 48
    • 84981422000 scopus 로고
    • For an earlier report on the reaction of 1,2,4-pentatriene, see
    • For an earlier report on the reaction of 1,2,4-pentatriene, see: Schneider, R.; Siegel, H.; Hopf, H. Liebigs Ann. Chem. 1981, 1812.
    • (1981) Liebigs Ann. Chem. , pp. 1812
    • Schneider, R.1    Siegel, H.2    Hopf, H.3
  • 51
    • 0024990690 scopus 로고
    • For a similar report applied to the study on DNA cleavage and antitumor activity, see
    • For a similar report applied to the study on DNA cleavage and antitumor activity, see: Nicolaou, K. C.; Maligres, P.; Shin, J.; de Leon, E.; Rideout, D. J. Am. Chem. Soc. 1990, 112, 7825.
    • (1990) Am. Chem. Soc. , vol.112 , pp. 7825
    • Nicolaou, K.C.1    Maligres, P.2    Shin, J.3    de Leon, E.4    Rideout, D.J.5
  • 72
    • 0032125895 scopus 로고    scopus 로고
    • For theoretical studies of these reactions, see
    • For theoretical studies of these reactions, see: Engels, B.; Hanrath, M. J. Am. Chem. Soc. 1998, 120, 6356.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 6356
    • Engels, B.1    Hanrath, M.2
  • 87
    • 0032560837 scopus 로고    scopus 로고
    • For intermolecular [4+2] cycloaddition of chloromethyl-sulfonyl (or trichloromethyl-sulfonyl)-l,2-propadiene with different 1,3-dienes, see
    • For intermolecular [4+2] cycloaddition of chloromethyl-sulfonyl (or trichloromethyl-sulfonyl)-l,2-propadiene with different 1,3-dienes, see: (b) Raj, C. P.; Dhas, N. A.; Cherkinski, M.; Gedanken, A.; Braverman, S. Tetrahedron Lett. 1998, 39, 5413.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 5413
    • Raj, C.P.1    Dhas, N.A.2    Cherkinski, M.3    Gedanken, A.4    Braverman, S.5
  • 125
    • 8844287597 scopus 로고    scopus 로고
    • For earlier reports with other reagents, see the references therein. For a review on the radical reaction of allenes, see
    • For earlier reports with other reagents, see the references therein. For a review on the radical reaction of allenes, see: Pan, F.; Fu, C.; Ma, S. Chin. J. Org. Chem. 2004, 24, 1168.
    • (2004) Chin. J. Org. Chem. , vol.24 , pp. 1168
    • Pan, F.1    Fu, C.2    Ma, S.3
  • 135
    • 22944431654 scopus 로고
    • For an early review, see
    • For an early review, see: Chan, T. H.; Ong, B. S. Tetrahedron Lett. 1980, 36, 2269.
    • (1980) Tetrahedron Lett. , vol.36 , pp. 2269
    • Chan, T.H.1    Ong, B.S.2
  • 148
    • 22944443399 scopus 로고    scopus 로고
    • Ionic Additions to Allenes
    • For a summary of early reports, see: Krause, N., Hashmi, A. S. K., Eds.; Wiley-VCH: Weinheim
    • For a summary of early reports, see: Ma, S. Ionic Additions to Allenes. In Modern Allene Chemistry; Krause, N., Hashmi, A. S. K., Eds.; Wiley-VCH: Weinheim, 2004.
    • (2004) Modern Allene Chemistry
    • Ma, S.1
  • 152
    • 0031971911 scopus 로고    scopus 로고
    • For recent reviews on Pauson-Khand reactions, see
    • For recent reviews on Pauson-Khand reactions, see: (a) Geis, O.; Schmalz, H.-G. Angew. Chem., Int. Ed. 1998, 37, 911.
    • (1998) Angew. Chem., Int. Ed. , vol.37 , pp. 911
    • Geis, O.1    Schmalz, H.-G.2
  • 175
    • 0002467340 scopus 로고    scopus 로고
    • For some early reports on the cyclometalation of two allenes, see
    • For some early reports on the cyclometalation of two allenes, see: (b) Hideura, D.; Urabe, H.; Sato, F. Chem. Commun. 1998, 271.
    • (1998) Chem. Commun. , pp. 271
    • Hideura, D.1    Urabe, H.2    Sato, F.3
  • 248
    • 0026031298 scopus 로고
    • For hydrostannylation of allenyl ether, see:
    • For hydrostannylation of allenyl ether, see: Koerber, K.; Gore, J.; Vatele, J.-M. Tetrahedron Lett. 1991, 32, 1187.
    • (1991) Tetrahedron Lett. , vol.32 , pp. 1187
    • Koerber, K.1    Gore, J.2    Vatele, J.-M.3
  • 254
    • 0036436669 scopus 로고    scopus 로고
    • For an intermolecular reaction of allenes and alcohols affording α,β-unsaturated enoates, see:
    • For an intermolecular reaction of allenes and alcohols affording α,β-unsaturated enoates, see: Zhou, D.-Y.; Yoneda, E.; Onitsuka, K.; Takahashi, S. Chem. Commun. 2002, 2868.
    • (2002) Chem. Commun. , pp. 2868
    • Zhou, D.-Y.1    Yoneda, E.2    Onitsuka, K.3    Takahashi, S.4
  • 316
    • 0032537088 scopus 로고    scopus 로고
    • For an early report on Pt-catalyzed diboration reaction of allenes, see:
    • For an early report on Pt-catalyzed diboration reaction of allenes, see: Ishiyama, T.; Kitano, T.; Miyaura, N. Tetrahedron Lett. 1998, 39, 2357.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 2357
    • Ishiyama, T.1    Kitano, T.2    Miyaura, N.3
  • 334
    • 16544375892 scopus 로고    scopus 로고
    • For a recent review in this area, see:
    • For a recent review in this area, see: Barbero, A.; Pulido, F. J. Synthesis 2004, 779.
    • (2004) Synthesis , pp. 779
    • Barbero, A.1    Pulido, F.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.