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Volumn 54, Issue 1, 2011, Pages 56-60

Synthesis of bromoallenyl pyrrolidines via 1,4-addition to 1,3-enynes

Author keywords

allene; bromoallene; conjugated enynes; halocyclization; halogenation; pyrrolidine

Indexed keywords

ALLENE; BROMOALLENE; CONJUGATED ENYNES; HALOCYCLIZATION; PYRROLIDINES;

EID: 79251567685     PISSN: 16747291     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11426-010-4133-6     Document Type: Conference Paper
Times cited : (3)

References (19)
  • 1
    • 4544276732 scopus 로고    scopus 로고
    • Synthesis and properties of allenic natural products and pharmaceuticals
    • 10.1002/anie.200300628
    • A. Hoffmann-Röder N. Krause 2004 Synthesis and properties of allenic natural products and pharmaceuticals Angew Chem Int Ed 43 1196 1216 10.1002/anie.200300628
    • (2004) Angew Chem Int Ed , vol.43 , pp. 1196-1216
    • Hoffmann-Röder, A.1    Krause, N.2
  • 2
    • 0001620953 scopus 로고
    • Recent developments in allene chemistry
    • 1:CAS:528:DyaL2cXlvFSlsLs%3D 10.1016/S0040-4020(01)91289-X
    • D.J. Pasto 1984 Recent developments in allene chemistry Tetrahedron 40 2805 2827 1:CAS:528:DyaL2cXlvFSlsLs%3D 10.1016/S0040-4020(01)91289-X
    • (1984) Tetrahedron , vol.40 , pp. 2805-2827
    • Pasto, D.J.1
  • 3
    • 4544320494 scopus 로고    scopus 로고
    • Wiley-VCH Verlag GmbH & Co. KGaA Weinheim 10.1002/9783527619573
    • Krause N, Hashmi ASK. Modern Allene Chemistry. Weinheim: Wiley-VCH Verlag GmbH & Co. KGaA, 2004. Vol 1 and 2
    • (2004) Modern Allene Chemistry
    • Krause, N.1    Hashmi, A.S.K.2
  • 4
    • 22944485617 scopus 로고    scopus 로고
    • Some typical advances in the synthetic applications of allenes
    • 10.1021/cr020024j
    • S. Ma 2005 Some typical advances in the synthetic applications of allenes Chem Rev 105 2829 2872 10.1021/cr020024j
    • (2005) Chem Rev , vol.105 , pp. 2829-2872
    • Ma, S.1
  • 6
    • 47049108431 scopus 로고    scopus 로고
    • Base-catalyzed intramolecular hydroamination of conjugated enynes
    • 1:CAS:528:DC%2BD1cXltVyjsrY%3D 10.1021/ol800334m
    • W. Zhang J.B. Werness W. Tang 2008 Base-catalyzed intramolecular hydroamination of conjugated enynes Org Lett 10 2023 2026 1:CAS:528: DC%2BD1cXltVyjsrY%3D 10.1021/ol800334m
    • (2008) Org Lett , vol.10 , pp. 2023-2026
    • Zhang, W.1    Werness, J.B.2    Tang, W.3
  • 7
    • 62049085521 scopus 로고    scopus 로고
    • Intramolecular hydroamination of conjugated enynes
    • 1:CAS:528:DC%2BD1MXjs1ags70%3D 10.1016/j.tet.2008.09.045
    • W. Zhang J.B. Werness W.P. Tang 2009 Intramolecular hydroamination of conjugated enynes Tetrahedron 65 3090 3095 1:CAS:528:DC%2BD1MXjs1ags70%3D 10.1016/j.tet.2008.09.045
    • (2009) Tetrahedron , vol.65 , pp. 3090-3095
    • Zhang, W.1    Werness, J.B.2    Tang, W.P.3
  • 8
    • 0032487948 scopus 로고    scopus 로고
    • Electrophilic cyclization of unsaturated amides
    • 1:CAS:528:DyaK1cXmvV2qu7o%3D 10.1016/S0040-4020(98)00698-X
    • S. Robin G. Rousseau 1998 Electrophilic cyclization of unsaturated amides Tetrahedron 54 13681 13736 1:CAS:528:DyaK1cXmvV2qu7o%3D 10.1016/S0040-4020(98) 00698-X
    • (1998) Tetrahedron , vol.54 , pp. 13681-13736
    • Robin, S.1    Rousseau, G.2
  • 9
    • 4444307147 scopus 로고    scopus 로고
    • Iodine electrophiles in stereoselective reactions: Recent developments and synthetic applications
    • 1:CAS:528:DC%2BD2cXmtVWgur8%3D 10.1039/b310389g
    • A.N. French S. Bissmire T. Wirth 2004 Iodine electrophiles in stereoselective reactions: Recent developments and synthetic applications Chem Soc Rev 33 354 362 1:CAS:528:DC%2BD2cXmtVWgur8%3D 10.1039/b310389g
    • (2004) Chem Soc Rev , vol.33 , pp. 354-362
    • French, A.N.1    Bissmire, S.2    Wirth, T.3
  • 10
    • 0000180210 scopus 로고
    • Biomimetic synthesis of (+/-) panacene
    • 1:CAS:528:DyaL3sXhs1Crsw%3D%3D 10.1016/S0040-4039(00)87525-5
    • K.S. Feldman 1982 Biomimetic synthesis of (+/-) panacene Tetrahedron Lett 23 3031 3034 1:CAS:528:DyaL3sXhs1Crsw%3D%3D 10.1016/S0040-4039(00)87525-5
    • (1982) Tetrahedron Lett , vol.23 , pp. 3031-3034
    • Feldman, K.S.1
  • 11
    • 0019977619 scopus 로고
    • Total synthesis of (+/-)-panacene
    • 1:CAS:528:DyaL38XltFShsrY%3D 10.1021/ja00378a042
    • K.S. Feldman C.C. Mechem L. Nader 1982 Total synthesis of (+/-)-panacene J Am Chem Soc 104 4011 4012 1:CAS:528:DyaL38XltFShsrY%3D 10.1021/ja00378a042
    • (1982) J Am Chem Soc , vol.104 , pp. 4011-4012
    • Feldman, K.S.1    Mechem, C.C.2    Nader, L.3
  • 12
    • 33747275056 scopus 로고    scopus 로고
    • Asymmetric total synthesis of (-)-panacene and correction of its relative configuration
    • 1:CAS:528:DC%2BD28Xms1SltLY%3D 10.1021/ol061385e
    • J. Boukouvalas M. Pouliot J. Robichaud S. Macneil V. Snieckus 2006 Asymmetric total synthesis of (-)-panacene and correction of its relative configuration Org Lett 8 3597 3599 1:CAS:528:DC%2BD28Xms1SltLY%3D 10.1021/ol061385e
    • (2006) Org Lett , vol.8 , pp. 3597-3599
    • Boukouvalas, J.1    Pouliot, M.2    Robichaud, J.3    MacNeil, S.4    Snieckus, V.5
  • 13
    • 0030991887 scopus 로고    scopus 로고
    • Conversion of prelaureatin into laurallene, a bromo-allene compound, by enzymatic and chemical bromo-etherification reactions
    • 1:CAS:528:DyaK2sXkt12ktLg%3D 10.1016/S0040-4020(97)00542-5
    • J. Ishihara Y. Shimada N. Kanoh Y. Takasugi A. Fukuzawa A. Murai 1997 Conversion of prelaureatin into laurallene, a bromo-allene compound, by enzymatic and chemical bromo-etherification reactions Tetrahedron 53 8371 8382 1:CAS:528:DyaK2sXkt12ktLg%3D 10.1016/S0040-4020(97)00542-5
    • (1997) Tetrahedron , vol.53 , pp. 8371-8382
    • Ishihara, J.1    Shimada, Y.2    Kanoh, N.3    Takasugi, Y.4    Fukuzawa, A.5    Murai, A.6
  • 14
    • 0034647232 scopus 로고    scopus 로고
    • Total synthesis of (+)-prelaureatin and (+)-laurallene
    • 1:CAS:528:DC%2BD3cXjsFGqsLo%3D 10.1021/ja0007197
    • M.T. Crimmins E.A. Tabet 2000 Total synthesis of (+)-prelaureatin and (+)-laurallene J Am Chem Soc 122 5473 5476 1:CAS:528:DC%2BD3cXjsFGqsLo%3D 10.1021/ja0007197
    • (2000) J Am Chem Soc , vol.122 , pp. 5473-5476
    • Crimmins, M.T.1    Tabet, E.A.2
  • 15
    • 0345476898 scopus 로고    scopus 로고
    • Enantioselective total synthesis of the nonisoprenoid sesquiterpene (-)-kumausallene
    • 1:CAS:528:DyaK1MXns1aqsb4%3D 10.1002/(SICI)1521-3773(19991102)38: 21<3175::AID-ANIE3175>3.0.CO;2-M
    • P.A. Evans V.S. Murthy J.D. Roseman A.L. Rheingold 1999 Enantioselective total synthesis of the nonisoprenoid sesquiterpene (-)-kumausallene Angew Chem Int Ed 38 3175 3177 1:CAS:528:DyaK1MXns1aqsb4%3D 10.1002/(SICI)1521- 3773(19991102)38:21<3175::AID-ANIE3175>3.0.CO;2-M
    • (1999) Angew Chem Int Ed , vol.38 , pp. 3175-3177
    • Evans, P.A.1    Murthy, V.S.2    Roseman, J.D.3    Rheingold, A.L.4
  • 17
    • 58149144453 scopus 로고    scopus 로고
    • Expeditious total syntheses of natural allenic products via aromatic ring umpolung
    • 1:CAS:528:DC%2BD1cXhtFeqs7vP 10.1021/ol801921d
    • C. Sabot D. Berard S. Canesi 2008 Expeditious total syntheses of natural allenic products via aromatic ring umpolung Org Lett 10 4629 4632 1:CAS:528:DC%2BD1cXhtFeqs7vP 10.1021/ol801921d
    • (2008) Org Lett , vol.10 , pp. 4629-4632
    • Sabot, C.1    Berard, D.2    Canesi, S.3
  • 18
    • 67849091011 scopus 로고    scopus 로고
    • Dabco-catalyzed 1,4-bromolactonization of conjugated enynes: Highly stereoselective formation of a stereogenic center and an axially chiral allene
    • 1:CAS:528:DC%2BD1MXisVCitrY%3D 10.1021/ja8099008
    • W. Zhang H.D. Xu H. Xu W.P. Tang 2009 Dabco-catalyzed 1,4-bromolactonization of conjugated enynes: Highly stereoselective formation of a stereogenic center and an axially chiral allene J Am Chem Soc 131 3832 3833 1:CAS:528:DC%2BD1MXisVCitrY%3D 10.1021/ja8099008
    • (2009) J Am Chem Soc , vol.131 , pp. 3832-3833
    • Zhang, W.1    Xu, H.D.2    Xu, H.3    Tang, W.P.4
  • 19
    • 77949791576 scopus 로고    scopus 로고
    • Enantioselective bromolactonization of conjugated (Z)-enynes
    • 1:CAS:528:DC%2BC3cXisFGmt7o%3D 10.1021/ja100173w
    • W. Zhang S.Q. Zheng N. Liu J.B. Werness I.A. Guzei W.P. Tang 2010 Enantioselective bromolactonization of conjugated (Z)-enynes J Am Chem Soc 132 3664 3665 1:CAS:528:DC%2BC3cXisFGmt7o%3D 10.1021/ja100173w
    • (2010) J Am Chem Soc , vol.132 , pp. 3664-3665
    • Zhang, W.1    Zheng, S.Q.2    Liu, N.3    Werness, J.B.4    Guzei, I.A.5    Tang, W.P.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.