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Volumn 43, Issue , 2013, Pages 21-50

The mechanism for transition-metal-catalyzed hydrochalcogenation of unsaturated organic molecules

Author keywords

Hydrochalcogenation; Oxidative addition; Protonolysis; Reductive elimination; Transition metal

Indexed keywords


EID: 84869077106     PISSN: 14366002     EISSN: None     Source Type: Book Series    
DOI: 10.1007/3418-2011-16     Document Type: Article
Times cited : (21)

References (68)
  • 1
    • 4444376920 scopus 로고    scopus 로고
    • Transition-metal-catalyzed addition of heteroatomhydrogen bonds to alkynes
    • Alonso F, Beletskaya IP, Yus M (2004) Transition-metal-catalyzed addition of heteroatomhydrogen bonds to alkynes. Chem Rev 104:3079-3159
    • (2004) Chem Rev , vol.104 , pp. 3079-3159
    • Alonso, F.1    Beletskaya, I.P.2    Yus, M.3
  • 2
    • 0001034345 scopus 로고    scopus 로고
    • Element-element addition to alkynes catalyzed by the group 10 metals
    • Beletskaya I, Moberg C (1999) Element-element addition to alkynes catalyzed by the group 10 metals. Chem Rev 99:3435-3461 (Pubitemid 129589125)
    • (1999) Chemical Reviews , vol.99 , Issue.12 , pp. 3435-3461
    • Beletskaya, I.1    Moberg, C.2
  • 3
    • 34447535455 scopus 로고    scopus 로고
    • Unusual influence of the structures of transition metal complexes on catalytic C-S and C-Se bond formation under homogenous and heterogeneous conditions
    • Beletskaya IP, Ananikov VP (2007) Unusual influence of the structures of transition metal complexes on catalytic C-S and C-Se bond formation under homogenous and heterogeneous conditions. Eur J Org Chem 3431-3444
    • (2007) Eur J Org Chem , pp. 3431-3444
    • Beletskaya, I.P.1    Ananikov, V.P.2
  • 4
    • 0033531468 scopus 로고    scopus 로고
    • Transition metal-catalysed addition reactions of H-heteroatom and inter-heteroatom bonds to carbon-carbon unsaturated linkages via oxidative additions
    • Han L-B, Tanaka M (1999) Transition-metal-catalyzed addition reactions of H-heteroatom and inter-heteroatom bonds to carbon-carbon unsaturated linkages via oxidative additions. Chem Commun 395-402 (Pubitemid 29116871)
    • (1999) Chemical Communications , Issue.5 , pp. 395-402
    • Han, L.-B.1    Tanaka, M.2
  • 5
    • 33847668926 scopus 로고    scopus 로고
    • Transition metal-catalyzed carbochalcogenation of alkynes
    • Kuniyasu H, Kambe N (2006) Transition metal-catalyzed carbochalcogenation of alkynes. Chem Lett 35:1320-1325
    • (2006) Chem Lett , vol.35 , pp. 1320-1325
    • Kuniyasu, H.1    Kambe, N.2
  • 6
    • 0037124565 scopus 로고    scopus 로고
    • Transition-metal-catalyzed carbon-heteroatom three-component cross-coupling reactions: A new concept for carbothiolation of alkynes
    • DOI 10.1002/1521-3765(20020617)8:12<2660::AID-CHEM2660>3.0.CO;2-Q
    • Kuniyasu H, Kurosawa H (2002) Transition-metal-catalyzed carbon-heteroatom three-component cross-coupling reactions: a new concept for carbothiolation of alkynes. Chem Eur J 8:2660-2665 (Pubitemid 34693288)
    • (2002) Chemistry - A European Journal , vol.8 , Issue.12 , pp. 2660-2665
    • Kuniyasu, H.1    Kurosawa, H.2
  • 7
    • 70349881729 scopus 로고    scopus 로고
    • Organometallics using organosulfur compounds: Exchange of information between catalytic and stoichiometric reactions
    • Kuniyasu H, Kambe N (2009) Organometallics using organosulfur compounds: exchange of information between catalytic and stoichiometric reactions. J Synth Org Chem Jpn 67:701-713
    • (2009) J Synth Org Chem Jpn , vol.67 , pp. 701-713
    • Kuniyasu, H.1    Kambe, N.2
  • 8
    • 79952644604 scopus 로고    scopus 로고
    • Transition-metal-catalyzed C-S, C-Se, and C-Te bond formation via cross-coupling and atom-economic addition reactions addition reactions
    • Beletskaya IP, Ananikov VP (2011) Transition-metal-catalyzed C-S, C-Se, and C-Te bond formation via cross-coupling and atom-economic addition reactions. Chem Rev 111:1596-1636
    • (2011) Chem Rev , vol.111 , pp. 1596-1636
    • Beletskaya, I.P.1    Ananikov, V.P.2
  • 10
    • 78649587563 scopus 로고    scopus 로고
    • Gold-catalyzed addition of X-H bonds to C-C multiple bonds
    • Hashmi AKS, Bührle M (2010) Gold-catalyzed addition of X-H bonds to C-C multiple bonds. Aldrichimica Acta 43:27-33
    • (2010) Aldrichimica Acta , vol.43 , pp. 27-33
    • Hashmi, A.K.S.1    Bührle, M.2
  • 11
    • 46649107683 scopus 로고    scopus 로고
    • Regioselective transformation of alkynes into cyclic acetals and thioacetals with a gold(I) catalyst: Comparison with Brønsted acid catalysts
    • Santos LL, Ruiz VR, Sabater MJ, Corma A (2008) Regioselective transformation of alkynes into cyclic acetals and thioacetals with a gold(I) catalyst: comparison with Brønsted acid catalysts. Tetrahedron 64:7902-7909
    • (2008) Tetrahedron , vol.64 , pp. 7902-7909
    • Santos, L.L.1    Ruiz, V.R.2    Sabater, M.J.3    Corma, A.4
  • 12
    • 3543083464 scopus 로고    scopus 로고
    • Platinum-catalyzed intramolecular hydroalkoxylation of γ- and δ-hydroxy olefins to form cyclic ethers
    • DOI 10.1021/ja0477773
    • Qian H, Han X, Widenhoefer RA (2004) Platinum-catalyzed intramolecular hydroalkoxylation of γ and δ hydroxy olefins to form cyclic ethers. J Am Chem Soc 126:9536-9537 (Pubitemid 39031029)
    • (2004) Journal of the American Chemical Society , vol.126 , Issue.31 , pp. 9536-9537
    • Qian, H.1    Han, X.2    Widenhoefer, R.A.3
  • 13
    • 33746048429 scopus 로고    scopus 로고
    • Highly active Au(I) catalyst for the intramolecular exo- hydrofunctionalization of allenes with carbon, nitrogen, and oxygen nucleophiles
    • DOI 10.1021/ja062045r
    • Zhang Z, Liu C, Kinder RE, Han X, Qian H, Widenhoefer RA (2006) Highly active Au(I) catalyst for the intramolecular exo-hydrofunctionalization of allenes with carbon, nitrogen, and oxygen nucleophiles. J Am Chem Soc 128:9066-9073 (Pubitemid 44078989)
    • (2006) Journal of the American Chemical Society , vol.128 , Issue.28 , pp. 9066-9073
    • Zhang, Z.1    Liu, C.2    Kinder, R.E.3    Han, X.4    Qian, H.5    Widenhoefer, R.A.6
  • 14
    • 46049088039 scopus 로고    scopus 로고
    • Regio- and stereoselective synthesis of alkyl allylic ethers via gold(I)-catalyzed intermolecular hydroalkoxylation of allenes with alcohols
    • Zhang Z, Widenhoefer RA (2008) Regio- and stereoselective synthesis of alkyl allylic ethers via gold(I)-catalyzed intermolecular hydroalkoxylation of allenes with alcohols. Org Lett 10:2079-2081
    • (2008) Org Lett , vol.10 , pp. 2079-2081
    • Zhang, Z.1    Widenhoefer, R.A.2
  • 15
    • 27144523211 scopus 로고    scopus 로고
    • Intramolecular additions of alcohols and carboxylic acids to inert olefins catalyzed by silver(I) triflate
    • DOI 10.1021/ol051065f
    • Yang C-G, Reich NW, Shi Z, He C (2005) Intramolecular additions of alcohols and carboxylic acids to inert olefins catalyzed by silver(I) triflate. Org Lett 7:4553-4556 (Pubitemid 41507040)
    • (2005) Organic Letters , vol.7 , Issue.21 , pp. 4553-4556
    • Yang, C.-G.1    Reich, N.W.2    Shi, Z.3    He, C.4
  • 16
    • 33846338769 scopus 로고    scopus 로고
    • Synthesis of functionalized THF and THP through Au-catalyzed cyclization of acetylenic alcohols
    • DOI 10.1016/j.tetlet.2006.12.100, PII S0040403906025469
    • Harkat H, Weibel J-M, Pale P (2007) Synthesis of functionalized THF and THP through Au-catalyzed cyclization of acetylenic alcohols. Tetrahedron Lett 48:1439-1442 (Pubitemid 46136393)
    • (2007) Tetrahedron Letters , vol.48 , Issue.8 , pp. 1439-1442
    • Harkat, H.1    Weibel, J.-M.2    Pale, P.3
  • 17
    • 46049101430 scopus 로고    scopus 로고
    • Gold-catalyzed intermolecular hydroalkoxylation of allenes; difference in mechanism between hydroalkoxylation and hydroamination
    • DOI 10.1016/j.tetlet.2008.05.152, PII S0040403908010836
    • Nishina N, Yamamoto Y (2008) Gold-catalyzed intermolecular hydroalkoxylation of allenes; difference in mechanism between hydroalkoxylation and hydroamination. Tetrahedron Lett 49:4908-4911 (Pubitemid 351899070)
    • (2008) Tetrahedron Letters , vol.49 , Issue.33 , pp. 4908-4911
    • Nishina, N.1    Yamamoto, Y.2
  • 18
    • 58949102784 scopus 로고    scopus 로고
    • Gold-catalyzed hydrofunctionalization of allenes with nitrogen and oxygen nucleophiles and its mechanistic insight
    • Nishina N, Yamamoto Y (2009) Gold-catalyzed hydrofunctionalization of allenes with nitrogen and oxygen nucleophiles and its mechanistic insight. Tetrahedron 65:1799-1808
    • (2009) Tetrahedron , vol.65 , pp. 1799-1808
    • Nishina, N.1    Yamamoto, Y.2
  • 19
    • 0032803182 scopus 로고    scopus 로고
    • Cycloisomerization of alkynols at transition metal templates
    • Weyershausen B, Dotz KH (1999) Cycloisomerization of alkynols at transition metal templates. Eur J Inorg Chem 1057-1066
    • (1999) Eur J Inorg Chem , pp. 1057-1066
    • Weyershausen, B.1    Dotz, K.H.2
  • 20
    • 0027752861 scopus 로고
    • A new synthesis of 2,3-dihydrofurans: Cycloisomerization of alkynyl alcohols to endocyclic enol ethers
    • DOI 10.1021/jo00077a006
    • McDonald FE, Connolly CB, Gleason MM, Towne TB, Treiber KD (1993) A new synthesis of 2,3-dihydrofurans: cycloisomerization alkynyl alcohols to endocyclic enol ethers. J Org Chem 58:6952-6953 (Pubitemid 24015766)
    • (1993) Journal of Organic Chemistry , vol.58 , Issue.25 , pp. 6952-6953
    • McDonald, F.E.1    Connolly, C.B.2    Gleason, M.M.3    Towne, T.B.4    Treiber, K.D.5
  • 21
    • 0026707559 scopus 로고
    • The first example of transitionmetal- catalyzed hydroselenation of acetylenes
    • Kuniyasu H, Ogawa A, Sato K-I, Ryu I, Sonoda N (1992) The first example of transitionmetal- catalyzed hydroselenation of acetylenes. Tetrahedron Lett 33:5525-5528
    • (1992) Tetrahedron Lett , vol.33 , pp. 5525-5528
    • Kuniyasu, H.1    Ogawa, A.2    Sato, K.-I.3    Ryu, I.4    Sonoda, N.5
  • 22
    • 0001664696 scopus 로고
    • The first example of transition-metal-catalyzed addition of aromatic thiols to acetylenes
    • Kuniyasu H, Ogawa A, Sato K-I, Ryu I, Kambe N, Sonoda N (1992) The first example of transition-metal-catalyzed addition of aromatic thiols to acetylenes. J Am Chem Soc 114:5902-5903
    • (1992) J Am Chem Soc , vol.114 , pp. 5902-5903
    • Kuniyasu, H.1    Ogawa, A.2    Sato, K.-I.3    Ryu, I.4    Kambe, N.5    Sonoda, N.6
  • 23
    • 12344312905 scopus 로고    scopus 로고
    • Palladium(II) acetate in pyridine as an effective catalyst for highly regioselective hydroselenation of alkynes
    • DOI 10.1021/jo048727j
    • Kamiya I, Nishinaka E, Ogawa A (2005) Palladium(II) acetate in pyridine as an efficient catalyst for highly regioselecitve hydroselenation of alkynes. J Org Chem 70:696-698 (Pubitemid 40129438)
    • (2005) Journal of Organic Chemistry , vol.70 , Issue.2 , pp. 696-698
    • Kamiya, I.1    Nishinaka, E.2    Ogawa, A.3
  • 24
    • 0033538289 scopus 로고    scopus 로고
    • Highly regio- and stereocontrolled synthesis of vinyl sulfides via transition-metal-catalyzed hydrothiolation of alkynes with thiols
    • DOI 10.1021/ja983949i
    • Ogawa A, Ikeda T, Kimura K, Hirao T (1999) Highly regio- and stereocontrolled synthesis of vinyl sulfides via transition-metal-catalyzed hydrothiolation of alkynes with thiols. J Am Chem Soc 121:5108-5114 (Pubitemid 29275716)
    • (1999) Journal of the American Chemical Society , vol.121 , Issue.22 , pp. 5108-5114
    • Ogawa, A.1    Ikeda, T.2    Kimura, K.3    Hirao, T.4
  • 25
    • 78649888068 scopus 로고    scopus 로고
    • Highly regioselective hydroselenation and double-bond isomerization of terminal alkynes with benzeneselenol catalyzed by bis(triphenylphosphine) palladium(II) dichloride
    • Ozaki T, Kotani M, Kusano H, Nomoto A, Ogawa A (2011) Highly regioselective hydroselenation and double-bond isomerization of terminal alkynes with benzeneselenol catalyzed by bis(triphenylphosphine)palladium(II) dichloride. J Organomet Chem 696:450-455
    • (2011) J Organomet Chem , vol.696 , pp. 450-455
    • Ozaki, T.1    Kotani, M.2    Kusano, H.3    Nomoto, A.4    Ogawa, A.5
  • 26
    • 34147123642 scopus 로고    scopus 로고
    • Palladium-catalyzed anti-hydrothiolation of 1-alkynylphosphines
    • Kondoh A, Yorimitsu H, Oshima K (2007) Palladium-catalyzed anti-hydrothiolation of 1-alkynylphosphines. Org Lett 9:1383-1385
    • (2007) Org Lett , vol.9 , pp. 1383-1385
    • Kondoh, A.1    Yorimitsu, H.2    Oshima, K.3
  • 28
    • 33646373908 scopus 로고    scopus 로고
    • Efficient and convenient synthesis of β-vinyl sulfides in nickel-catalyzed regioselective addition of thiols to terminal alkynes under solvent-free conditions
    • DOI 10.1021/om051105j
    • Ananikov VP, Orlov NV, Beletskaya IP (2006) Efficient and convenient synthesis of b-vinyl sulfides in nickel-catalyzed regioselective addition of thiols to terminal alkynes under solventfree conditions. Organometallics 25:1970-1977 (Pubitemid 43672819)
    • (2006) Organometallics , vol.25 , Issue.8 , pp. 1970-1977
    • Ananikov, V.P.1    Orlov, N.V.2    Beletskaya, I.P.3
  • 29
    • 34247170535 scopus 로고    scopus 로고
    • Nickel-catalyzed addition of benzenethiol to alkynes: Formation of carbon-sulfur and carbon-carbon bonds
    • Ananikov VP, Zalesskiy SS, Orlev NV, Beletskaya IP (2006) Nickel-catalyzed addition of benzenethiol to alkynes: formation of carbon-sulfur and carbon-carbon bonds. Russ Chem Bull Int Ed 55:2109-2133
    • (2006) Russ Chem Bull Int Ed , vol.55 , pp. 2109-2133
    • Ananikov, V.P.1    Zalesskiy, S.S.2    Orlev, N.V.3    Beletskaya, I.P.4
  • 30
    • 33847211456 scopus 로고    scopus 로고
    • Highly efficient nickel-based heterogeneous catalytic system with nanosized structural organization for selective Se-H bond addition to terminal and internal alkynes
    • Ananikov VP, Orlev NV, Beletskaya IP (2007) Highly efficient nickel-based heterogeneous catalytic system with nanosized structural organization for selective Se-H bond addition to terminal and internal alkynes. Organometallics 26:740-750
    • (2007) Organometallics , vol.26 , pp. 740-750
    • Ananikov, V.P.1    Orlev, N.V.2    Beletskaya, I.P.3
  • 31
    • 33748807078 scopus 로고    scopus 로고
    • Homogeneous nickel catalysts for the selective transfer of a single arylthio group in the catalytic hydrothiolation of alkynes
    • DOI 10.1021/om060302v
    • Malyshev DA, Scott NM, Marion N, Stevens ED, Ananikov VP, Beletskaya IP, Nolan SP (2006) Homogeneous nickel catalysts for the selective transfer of a single arylthio group in the catalytic hydrothiolation of alkynes. Organometallics 25:4462-4470 (Pubitemid 44412260)
    • (2006) Organometallics , vol.25 , Issue.19 , pp. 4462-4470
    • Malyshev, D.A.1    Scott, N.M.2    Marion, N.3    Stevens, E.D.4    Ananikov, V.P.5    Beletskaya, I.P.6    Nolan, S.P.7
  • 32
    • 63449095003 scopus 로고    scopus 로고
    • Catalytic leaching as an efficient tool for constructing new catalytic reactions: Application to the synthesis of cyclic vinyl sulfides and vinyl selenides
    • Ananikov VP, Gayduk KA, Beletskaya IP, Khrustalev VN, Antipin MY (2009) Catalytic leaching as an efficient tool for constructing new catalytic reactions: application to the synthesis of cyclic vinyl sulfides and vinyl selenides. Eur J Inorg Chem 1149-1161
    • (2009) Eur J Inorg Chem , pp. 1149-1161
    • Ananikov, V.P.1    Gayduk, K.A.2    Beletskaya, I.P.3    Khrustalev, V.N.4    Antipin, M.Y.5
  • 33
    • 67849114613 scopus 로고    scopus 로고
    • Organoactinide-mediated hydrothiolation of terminal alkynes with aliphatic, aromatic, and benzylic thiols
    • Weiss CJ, Wobser SD, Marks TJ (2009) Organoactinide-mediated hydrothiolation of terminal alkynes with aliphatic, aromatic, and benzylic thiols. J Am Chem Soc 131:2062-2063
    • (2009) J Am Chem Soc , vol.131 , pp. 2062-2063
    • Weiss, C.J.1    Wobser, S.D.2    Marks, T.J.3
  • 34
    • 78649849420 scopus 로고    scopus 로고
    • Lanthanide- and actinide-mediated terminal alkyne hydrothiolation for the catalytic synthesis of Markovnikov vinyl sulfides
    • Weiss CJ, Wobser SD, Marks TJ (2010) Lanthanide- and actinide-mediated terminal alkyne hydrothiolation for the catalytic synthesis of Markovnikov vinyl sulfides. Organometallics 29:6308-6320
    • (2010) Organometallics , vol.29 , pp. 6308-6320
    • Weiss, C.J.1    Wobser, S.D.2    Marks, T.J.3
  • 35
    • 77956193621 scopus 로고    scopus 로고
    • Organozirconium complexes as catalysts for Markovnikovselective intermolecular hydrothiolation of terminal alkynes: Scope and mechanism
    • Weiss CJ, Marks TJ (2010) Organozirconium complexes as catalysts for Markovnikovselective intermolecular hydrothiolation of terminal alkynes: scope and mechanism. J Am Chem Soc 132:10533-10546
    • (2010) J Am Chem Soc , vol.132 , pp. 10533-10546
    • Weiss, C.J.1    Marks, T.J.2
  • 36
    • 34250881661 scopus 로고    scopus 로고
    • Effective, selective hydroalkoxylation/cyclization of alkynyl and allenyl alcohols mediated by lanthanide catalysts
    • DOI 10.1021/ja071707p
    • Yu X, Seo SY, Marks TJ (2007) Effective, selective hydroalkoxylation/ cyclization of alkynyl and allenyl alcohols mediated by lanthanide catalysts. J Am Chem Soc 129:7244-7245 (Pubitemid 46980789)
    • (2007) Journal of the American Chemical Society , vol.129 , Issue.23 , pp. 7244-7245
    • Yu, X.1    Seo, S.2    Marks, T.J.3
  • 37
    • 62649160608 scopus 로고    scopus 로고
    • Intramolecular hydroalkoxylation/cyclization of alkynyl alcohols mediated by lanthanide Catalysts. Scope and reaction mechanism
    • Seo SY, Yu X, Marks TJ (2009) Intramolecular hydroalkoxylation/ cyclization of alkynyl alcohols mediated by lanthanide Catalysts. Scope and reaction mechanism. J Am Chem Soc 131:263-276
    • (2009) J Am Chem Soc , vol.131 , pp. 263-276
    • Seo, S.Y.1    Yu, X.2    Marks, T.J.3
  • 38
    • 77951847682 scopus 로고    scopus 로고
    • Atom-efficient carbon-oxygen bond formation processes. DFT analysis of the intramolecular hydroalkoxylation/cyclization of alkynyl alcohols mediated by lanthanide catalysts
    • Motta A, Fragalà IL, Marks TJ (2010) Atom-efficient carbon-oxygen bond formation processes. DFT analysis of the intramolecular hydroalkoxylation/cyclization of alkynyl alcohols mediated by lanthanide catalysts. Organometallics 29:2004-2012
    • (2010) Organometallics , vol.29 , pp. 2004-2012
    • Motta, A.1    Fragalà, I.L.2    Marks, T.J.3
  • 39
    • 77951557943 scopus 로고    scopus 로고
    • Lanthanide-catalyst-mediated tandem double intramolecular hydroalkoxylation/cyclization of dialkynyl dialcohols: Scope and mechanism
    • Seo SY, Marks TB (2010) Lanthanide-catalyst-mediated tandem double intramolecular hydroalkoxylation/cyclization of dialkynyl dialcohols: scope and mechanism. Chem Eur J 16:5148-5162
    • (2010) Chem Eur J , vol.16 , pp. 5148-5162
    • Seo, S.Y.1    Marks, T.B.2
  • 40
    • 64349115503 scopus 로고    scopus 로고
    • Efficient intramolecular hydroalkoxylation/cyclization of unactivated alkenols mediated by lanthanide triflate ionic liquids
    • Dzudza A, Marks TJ (2009) Efficient intramolecular hydroalkoxylation/ cyclization of unactivated alkenols mediated by lanthanide triflate ionic liquids. Org Lett 11:1523-1526
    • (2009) Org Lett , vol.11 , pp. 1523-1526
    • Dzudza, A.1    Marks, T.J.2
  • 41
    • 77949291993 scopus 로고    scopus 로고
    • Efficient intramolecular hydroalkoxylation of unactivated alkenols mediated by recyclable lanthanide triflate ionic liquids: Scope and mechanism
    • Dzudza A, Marks TJ (2010) Efficient intramolecular hydroalkoxylation of unactivated alkenols mediated by recyclable lanthanide triflate ionic liquids: scope and mechanism. Chem Eur J 16:3403-3422
    • (2010) Chem Eur J , vol.16 , pp. 3403-3422
    • Dzudza, A.1    Marks, T.J.2
  • 42
    • 77954719687 scopus 로고    scopus 로고
    • Organo-f-element catalysts for efficient and highly selective hydroalkoxylation and hydrothiolation
    • Weiss CJ, Marks TJ (2010) Organo-f-element catalysts for efficient and highly selective hydroalkoxylation and hydrothiolation. Dalton Trans 39:6576-6588
    • (2010) Dalton Trans , vol.39 , pp. 6576-6588
    • Weiss, C.J.1    Marks, T.J.2
  • 43
    • 77951536172 scopus 로고    scopus 로고
    • Mechanistic exploration of the intramolecular hydroalkoxylation of allenyl alcohols mediated by organolanthanide complexes: A DFT study
    • Tobisch S (2010) Mechanistic exploration of the intramolecular hydroalkoxylation of allenyl alcohols mediated by organolanthanide complexes: a DFT study. Chem Eur J 16:4955-4998
    • (2010) Chem Eur J , vol.16 , pp. 4955-4998
    • Tobisch, S.1
  • 44
    • 85047285903 scopus 로고    scopus 로고
    • Highly regioselective hydrothiocarboxylation of acetylenes with carbon monoxide and thiols catalyzed by Pt(PPh4)4
    • Ogawa A, Kawakami J-i, Mihara M, Ikeda T, Sonoda N, Hirao T (1997) Highly regioselective hydrothiocarboxylation of acetylenes with carbon monoxide and thiols catalyzed by Pt(PPh4)4. J Am Chem Soc 119:12380-12381
    • (1997) J Am Chem Soc , vol.119 , pp. 12380-12381
    • Ogawa, A.1    K, J.-I.2    Mihara, M.3    Ikeda, T.4    Sonoda, N.5    Hirao, T.6
  • 47
    • 28844448397 scopus 로고
    • Platinum (0)-catalysed hydrophosphination of acrylonitrile
    • Pringle PG, Smith MB (1990) Platinum(0)-catalysed hydrophosphination of acrylonitrile. J Chem Soc Chem Commun 1701-1702
    • (1990) J Chem Soc Chem Commun , pp. 1701-1702
    • Pringle, P.G.1    Smith, M.B.2
  • 49
    • 53849148938 scopus 로고    scopus 로고
    • Insertion of alkynes into an ArS-Pt bond: Regio- and Stereoselective thermal reactions, facilitation by "o-halogen effect" and photoirradiation, different alkyne preferences depending on the ancillary ligand, and application to a catalytic reaction
    • Kuniyasu H, Takekawa K, Yamashita F, Miyafuji K, Asano S, Takai Y, Ohtaka A, Tanaka A, Sugoh K, Kurosawa H, Kambe N (2008) Insertion of alkynes into an ArS-Pt bond: regio- and Stereoselective thermal reactions, facilitation by "o-halogen effect" and photoirradiation, different alkyne preferences depending on the ancillary ligand, and application to a catalytic reaction. Organometallics 27:4788-4802
    • (2008) Organometallics , vol.27 , pp. 4788-4802
    • Kuniyasu, H.1    Takekawa, K.2    Yamashita, F.3    Miyafuji, K.4    Asano, S.5    Takai, Y.6    Ohtaka, A.7    Tanaka, A.8    Sugoh, K.9    Kurosawa, H.10    Kambe, N.11
  • 50
    • 34547801790 scopus 로고    scopus 로고
    • Definitive evidence for the insertion of terminal alkynes into ArylS-Pt bonds: "O-halogen effect" in stoichiometric and catalytic reactions
    • DOI 10.1002/anie.200604986
    • Kuniyasu H, Yamashita F, Terao J, Kambe N (2007) Definitive evidence for the insertion of terminal alkynes into arylS-Pt bonds: "o-halogen effect" in stoichiometric and catalytic reactions. Angew Chem Int Ed 46:5929-5933 (Pubitemid 47236473)
    • (2007) Angewandte Chemie - International Edition , vol.46 , Issue.31 , pp. 5929-5933
    • Kuniyasu, H.1    Yamashita, F.2    Terao, J.3    Kambe, N.4
  • 51
    • 33645406778 scopus 로고    scopus 로고
    • The first definitive example of oxidative addition of acyclic vinyl selenide to M(0) complex
    • Kuniyasu H, Kato T, Inoue M, Terao J, Kambe N (2006) The first definitive example of oxidative addition of acyclic vinyl selenide to M(0) complex. J Organomet Chem 691:1873-1878
    • (2006) J Organomet Chem , vol.691 , pp. 1873-1878
    • Kuniyasu, H.1    Kato, T.2    Inoue, M.3    Terao, J.4    Kambe, N.5
  • 52
    • 0035982968 scopus 로고    scopus 로고
    • The insertion of dimethyl acetylenedicarboxylate into an S-Pd bond
    • Sugoh K, Kuniyasu H, Kurosawa H (2002) The insertion of dimethyl acetylenedicarboxylate into an S-Pd bond. Chem Lett 106-107
    • (2002) Chem Lett , pp. 106-107
    • Sugoh, K.1    Kuniyasu, H.2    Kurosawa, H.3
  • 53
    • 77949292190 scopus 로고    scopus 로고
    • Hydroselenation and carboselenation of electron-deficient alkynes with isolable (hydrido)(selenolato)platinum(II) complexes and a selenaplatinacycle bearing a triptycene skeleton
    • Ishii A, Kamon H, Murakami K, Nakata N (2010) Hydroselenation and carboselenation of electron-deficient alkynes with isolable (hydrido) (selenolato)platinum(II) complexes and a selenaplatinacycle bearing a triptycene skeleton. Eur J Org Chem 1653-1659
    • (2010) Eur J Org Chem , pp. 1653-1659
    • Ishii, A.1    Kamon, H.2    Murakami, K.3    Nakata, N.4
  • 54
    • 53549092263 scopus 로고    scopus 로고
    • Reactions of a ditriptycyl-substituted selenoseleninate and related compounds with a platinum(0) complex: Formation of selenaplatinacycle and hydrido selenolato platinum(II) complexes
    • Ishii A, Nakata N, Uchiumi R, Murakami K (2008) Reactions of a ditriptycyl-substituted selenoseleninate and related compounds with a platinum(0) complex: formation of selenaplatinacycle and hydrido selenolato platinum(II) complexes. Angew Chem Int Ed 47:2661-2664
    • (2008) Angew Chem Int Ed , vol.47 , pp. 2661-2664
    • Ishii, A.1    Nakata, N.2    Uchiumi, R.3    Murakami, K.4
  • 55
    • 77953005275 scopus 로고    scopus 로고
    • Synthesis and properties of hydrido(selenolato)platinum (II) complexes bearing chelating phosphine ligands
    • Nakata N, Yoshino T, Ishii A (2010) Synthesis and properties of hydrido(selenolato)platinum (II) complexes bearing chelating phosphine ligands. Phosphorus Sulfur Silicon Relat Elem 185:992-999
    • (2010) Phosphorus Sulfur Silicon Relat Elem , vol.185 , pp. 992-999
    • Nakata, N.1    Yoshino, T.2    Ishii, A.3
  • 56
    • 77954265690 scopus 로고    scopus 로고
    • Thermal reaction of a (hydrido)(selenolato)platinum (II) complex having a dibenzobarrelenyl group leading to three cyclometalations
    • Ishii A, Yamaguchi Y, Nakata N (2010) Thermal reaction of a (hydrido)(selenolato)platinum (II) complex having a dibenzobarrelenyl group leading to three cyclometalations. Dalton Trans 39:6181-6183
    • (2010) Dalton Trans , vol.39 , pp. 6181-6183
    • Ishii, A.1    Yamaguchi, Y.2    Nakata, N.3
  • 57
    • 77749314738 scopus 로고    scopus 로고
    • Synthesis and thermal reaction of hydrido(selenolato) platinum(II) complex having a 9,10,11,12,14,15-hexahydro-9,10[30, 40]-furanoanthracenyl group
    • Nakata N, Yamaguchi Y, Ishii A (2010) Synthesis and thermal reaction of hydrido(selenolato) platinum(II) complex having a 9,10,11,12,14,15-hexahydro-9, 10[30,40]-furanoanthracenyl group. J Organomet Chem 695:970-973
    • (2010) J Organomet Chem , vol.695 , pp. 970-973
    • Nakata, N.1    Yamaguchi, Y.2    Ishii, A.3
  • 58
    • 67650360823 scopus 로고    scopus 로고
    • Synthesis and X-ray structural analysis of hydrido(thiolato) platinum(II) complexes
    • Nakata N, Yamamoto S, Hashima W, Ishii A (2009) Synthesis and X-ray structural analysis of hydrido(thiolato) platinum(II) complexes. Chem Lett 38:400-401
    • (2009) Chem Lett , vol.38 , pp. 400-401
    • Nakata, N.1    Yamamoto, S.2    Hashima, W.3    Ishii, A.4
  • 59
    • 65349117584 scopus 로고    scopus 로고
    • Reactions of 9-triptyceneselenol with palladium (0) complexes: Unexpected formations of the dinuclear palladium(I) complex [{Pd(PPh3)}2(m-SeTrip)2] and five-membered selenapalladacycle [Pd(m2(C,Se)-Trip) (dppe)]
    • Nakata N, Uchiumi R, Yoshino T, Ikeda T, Kamon H, Ishii A (2009) Reactions of 9-triptyceneselenol with palladium(0) complexes: unexpected formations of the dinuclear palladium(I) complex [{Pd(PPh3)}2(m-SeTrip)2] and five-membered selenapalladacycle [Pd(m2(C,Se)-Trip) (dppe)]. Organometallics 28:1981-1984
    • (2009) Organometallics , vol.28 , pp. 1981-1984
    • Nakata, N.1    Uchiumi, R.2    Yoshino, T.3    Ikeda, T.4    Kamon, H.5    Ishii, A.6
  • 60
    • 77956252949 scopus 로고    scopus 로고
    • Syntheses of selenolato-bridged dinuclear hydridoplatinum complexes [Pt2H2(m-SetBu)2(PPh3)2] and [Pt2H(SetBu)(m-SetBu)2(PPh3)2]: Unusual thermal reaction of hydrido(1,1-dimethylethaneselenolato) platinum complex cis-[PtH(SetBu) (PPh3) 2]
    • Nakata N, Ikeda T, Ishii A (2010) Syntheses of selenolato-bridged dinuclear hydridoplatinum complexes [Pt2H2(m-SetBu)2(PPh3)2] and [Pt2H(SetBu)(m-SetBu)2(PPh3)2]: unusual thermal reaction of hydrido(1,1- dimethylethaneselenolato) platinum complex cis-[PtH(SetBu) (PPh3)2]. Inorg Chem 49:8112-8116
    • (2010) Inorg Chem , vol.49 , pp. 8112-8116
    • Nakata, N.1    Ikeda, T.2    Ishii, A.3
  • 61
    • 37049121347 scopus 로고
    • Oxidative addition of hydrogen cyanide, hydrogen sulphide, and other acids to triphenylphosphine complexes of iridium(I) and rhodium (I
    • Singer H, Wilkinson G (1968) Oxidative addition of hydrogen cyanide, hydrogen sulphide, and other acids to triphenylphosphine complexes of iridium(I) and rhodium(I). J Chem Soc A 2516-2520
    • (1968) J Chem Soc A , pp. 2516-2520
    • Singer, H.1    Wilkinson, G.2
  • 62
    • 36749052170 scopus 로고    scopus 로고
    • Catalytic alkyne hydrothiolation with alkanethiols using Wilkinson's catalyst
    • DOI 10.1021/om700811e
    • Shoai S, Bichler P, Kang B, Buckley H, Love JA (2007) Catalytic alkyne Hydrothiolation with alkanethiols using Wilkinson's catalyst. Organometallics 26:5778-5781 (Pubitemid 350208099)
    • (2007) Organometallics , vol.26 , Issue.24 , pp. 5778-5781
    • Shoai, S.1    Bichler, P.2    Kang, B.3    Buckley, H.4    Love, J.A.5
  • 63
    • 29344438415 scopus 로고    scopus 로고
    • Rhodium-catalyzed alkyne hydrothiolation with aromatic and aliphatic thiols
    • DOI 10.1021/ja055096h
    • Cao C, Fraser LR, Love JA (2005) Rhodium-catalyzed alkyne hydrothiolation with aromatic and aliphatic thiols. J Am Chem Soc 127:17614-17615 (Pubitemid 43003370)
    • (2005) Journal of the American Chemical Society , vol.127 , Issue.50 , pp. 17614-17615
    • Cao, C.1    Fraser, L.R.2    Love, J.A.3
  • 64
    • 36248964810 scopus 로고    scopus 로고
    • Synthesis, structure, and hydrothiolation activity of rhodium pyrazolylborate complexes
    • DOI 10.1021/om700564t
    • Fraser LR, Bird J, Wu Q, Cao C, Patrick BO, Love JA (2007) Synthesis, structure, and hydrothiolation activity of rhodium pyrazolylborate complexes. Organometallics 26:5602-5611 (Pubitemid 350132891)
    • (2007) Organometallics , vol.26 , Issue.23 , pp. 5602-5611
    • Fraser, L.R.1    Bird, J.2    Wu, Q.3    Cao, C.4    Patrick, B.O.5    Love, J.A.6
  • 65
    • 55949083132 scopus 로고    scopus 로고
    • Synthesis of 1,1-disubstituted olefins via catalytic alkyne Hydrothiolation/Kumada cross-coupling
    • Sabarre A, Love J (2008) Synthesis of 1,1-disubstituted olefins via catalytic alkyne Hydrothiolation/Kumada cross-coupling. Org Lett 10:3941-3944
    • (2008) Org Lett , vol.10 , pp. 3941-3944
    • Sabarre, A.1    Love, J.2
  • 66
    • 58149311074 scopus 로고    scopus 로고
    • Synthesis of 1,1-disubstituted alkyl vinyl sulfides via rhodium-catalyzed alkyne hydrothiolation: Scope and limitations
    • Yang J, Sabarre A, Fraser LR, Patrick BO, Love JA (2009) Synthesis of 1,1-disubstituted alkyl vinyl sulfides via rhodium-catalyzed alkyne hydrothiolation: scope and limitations. J Org Chem 74:182-187
    • (2009) J Org Chem , vol.74 , pp. 182-187
    • Yang, J.1    Sabarre, A.2    Fraser, L.R.3    Patrick, B.O.4    Love, J.A.5
  • 67
    • 0344980584 scopus 로고    scopus 로고
    • Rhodium(I) and iridium (I) complexes with bidentate N,N and P,N ligands as catalysts for the hydrothiolation of alkynes
    • Burling S, Field LD, Messerle BA, Vuong KQ, Turner P (2003) Rhodium(I) and iridium(I) complexes with bidentate N,N and P,N ligands as catalysts for the hydrothiolation of alkynes. Dalton Trans 4181-4191
    • (2003) Dalton Trans , pp. 4181-4191
    • Burling, S.1    Field, L.D.2    Messerle, B.A.3    Vuong, K.Q.4    Turner, P.5
  • 68
    • 65349125853 scopus 로고    scopus 로고
    • Rhodium(I) and iridium (I) complexes containing bidentate phosphine-imidazolyl donor ligands as catalysts for the hydroamination and hydrothiolation of alkynes
    • Field LD, Messerle BA, Vuong KQ, Turner P (2009) Rhodium(I) and iridium(I) complexes containing bidentate phosphine-imidazolyl donor ligands as catalysts for the hydroamination and hydrothiolation of alkynes. Dalton Trans 3599-3614
    • (2009) Dalton Trans , pp. 3599-3614
    • Field, L.D.1    Messerle, B.A.2    Vuong, K.Q.3    Turner, P.4


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