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Volumn 6, Issue , 2015, Pages

Asymmetric synthesis of N-allylic indoles via regio- and enantioselective allylation of aryl hydrazines

Author keywords

[No Author keywords available]

Indexed keywords

ARYL HYDRAZINE DERIVATIVE; HYDRAZINE DERIVATIVE; INDOLE DERIVATIVE; N ALLYLIC INDOLE; RHODIUM; TOLUENE; UNCLASSIFIED DRUG; 2,3 DIHYDRO 5 METHYL 3 (MORPHOLINOMETHYL) 6 (1 NAPHTHOYL)PYRROLO[1,2,3 DE][1,4]BENZOXAZINE; ALKADIENE; ALLYL COMPOUND; BENZOXAZINE DERIVATIVE; MORPHOLINE DERIVATIVE; NAPHTHALENE DERIVATIVE; PLANT EXTRACT; PROPADIENE; VINCAMINE; YUREMAMINE;

EID: 84936802731     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms8616     Document Type: Article
Times cited : (72)

References (46)
  • 1
    • 27844463013 scopus 로고    scopus 로고
    • Indole alkaloid marine natural products: An established source of cancer drug leads with considerable promise for the control of parasitic, neurological and other diseases
    • Gul, W. & Hamann, M. T. Indole alkaloid marine natural products: An established source of cancer drug leads with considerable promise for the control of parasitic, neurological and other diseases. Life Sci. 78, 442-453 (2005).
    • (2005) Life Sci. , vol.78 , pp. 442-453
    • Gul, W.1    Hamann, M.T.2
  • 2
    • 33745767359 scopus 로고    scopus 로고
    • Metabolic engineering of cell cultures versus whole plant complexity in production of bioactive monoterpene indole alkaloids: Recent progress related to old dilemma
    • Pasquali, G., Porto, D. D. & Fett-Neto, A. G. Metabolic engineering of cell cultures versus whole plant complexity in production of bioactive monoterpene indole alkaloids: Recent progress related to old dilemma. J. Biosci. Bioeng. 101, 287-296 (2006).
    • (2006) J. Biosci. Bioeng. , vol.101 , pp. 287-296
    • Pasquali, G.1    Porto, D.D.2    Fett-Neto, A.G.3
  • 3
    • 33746794215 scopus 로고    scopus 로고
    • Recent advances in the chemistry of macroline, sarpagine and ajmaline-related indole alkaloids
    • Lewis, S. E. Recent advances in the chemistry of macroline, sarpagine and ajmaline-related indole alkaloids. Tetrahedron 62, 8655-8681 (2006).
    • (2006) Tetrahedron , vol.62 , pp. 8655-8681
    • Lewis, S.E.1
  • 4
    • 33746520558 scopus 로고    scopus 로고
    • Chemistry and biology of monoterpene indole alkaloid biosynthesis
    • O'Connor, S. E. & Maresh, J. J. Chemistry and biology of monoterpene indole alkaloid biosynthesis. Nat. Prod. Rep. 23, 532-547 (2006).
    • (2006) Nat. Prod. Rep. , vol.23 , pp. 532-547
    • O'Connor, S.E.1    Maresh, J.J.2
  • 5
    • 34547095509 scopus 로고    scopus 로고
    • Simple indole alkaloids and those with a nonrearranged monoterpenoid unit
    • Higuichi, K. & Kawasaki, T. Simple indole alkaloids and those with a nonrearranged monoterpenoid unit. Nat. Prod. Rep. 24, 843-868 (2007).
    • (2007) Nat. Prod. Rep. , vol.24 , pp. 843-868
    • Higuichi, K.1    Kawasaki, T.2
  • 6
    • 77955673540 scopus 로고    scopus 로고
    • Marine indole alkaloids: Potential new drug leads for the control of depression and anxiety
    • Kochanowska-Karamyan, A. J. & Hamann, M. T. Marine indole alkaloids: Potential new drug leads for the control of depression and anxiety. Chem. Rev. 110, 4489-4497 (2010).
    • (2010) Chem. Rev. , vol.110 , pp. 4489-4497
    • Kochanowska-Karamyan, A.J.1    Hamann, M.T.2
  • 7
    • 0022966767 scopus 로고
    • Disposition kinetics and oral bioavailability of vincamine-loaded polyalkyl cyanoacrylate nanoparticles
    • Maincent, P., Verge, R. L., Sado, P., Couvreur, P. & Devissaguet, J. P. Disposition kinetics and oral bioavailability of vincamine-loaded polyalkyl cyanoacrylate nanoparticles. J. Pharm. Sci. 75, 955-958 (1986).
    • (1986) J. Pharm. Sci. , vol.75 , pp. 955-958
    • Maincent, P.1    Verge, R.L.2    Sado, P.3    Couvreur, P.4    Devissaguet, J.P.5
  • 8
    • 0342762087 scopus 로고    scopus 로고
    • The analgesic effects of R()-WIN 55, 212-2 mesylate, a high affinity cannabinoid agonist, in a rat model of neuropathic pain
    • Herzberg, U., Eliav, E., Bennett, G. J. & Kopin, I. J. The analgesic effects of R()-WIN 55, 212-2 mesylate, a high affinity cannabinoid agonist, in a rat model of neuropathic pain. Neurosci. Lett. 221, 157-160 (1997).
    • (1997) Neurosci. Lett. , vol.221 , pp. 157-160
    • Herzberg, U.1    Eliav, E.2    Bennett, G.J.3    Kopin, I.J.4
  • 9
    • 0031035975 scopus 로고    scopus 로고
    • Marine alkaloids. 19. Three new alkaloids, securamines E-G, from the marine bryozoan Securiflustra securifrons
    • Rahbæk, L. & Christophersen, C. Marine alkaloids. 19. Three new alkaloids, securamines E-G, from the marine bryozoan Securiflustra securifrons. J. Nat. Prod. 60, 175-177 (1997).
    • (1997) J. Nat. Prod. , vol.60 , pp. 175-177
    • Rahbæk, L.1    Christophersen, C.2
  • 11
    • 61449184626 scopus 로고    scopus 로고
    • Flinderoles A-C: Antimalarial bis-indole alkaloids from Flindersia species
    • Fernandez, L. S., Buchanan, M. S., Carroll, A. R., Feng, Y. J. & Quinn, R. J. Flinderoles A-C: Antimalarial bis-indole alkaloids from Flindersia species. Org. Lett. 11, 329-332 (2009).
    • (2009) Org. Lett. , vol.11 , pp. 329-332
    • Fernandez, L.S.1    Buchanan, M.S.2    Carroll, A.R.3    Feng, Y.J.4    Quinn, R.J.5
  • 12
    • 84884901821 scopus 로고    scopus 로고
    • On the biosynthesis and optical activity of the flinderoles
    • Vallakati, R., Smuts, J. P., Armstrong, D. W. & May, J. A. On the biosynthesis and optical activity of the flinderoles. Tetrahedron Lett. 54, 5892-5894 (2013).
    • (2013) Tetrahedron Lett. , vol.54 , pp. 5892-5894
    • Vallakati, R.1    Smuts, J.P.2    Armstrong, D.W.3    May, J.A.4
  • 13
    • 16844383145 scopus 로고    scopus 로고
    • Pd-catalyzed C3-selective allylation of indoles with allyl alcohols promoted by triethylborane
    • Kimura, M., Futamata, M., Mukai, R. & Tamaru, Y. Pd-catalyzed C3-selective allylation of indoles with allyl alcohols promoted by triethylborane. J. Am. Chem. Soc. 127, 4592-4593 (2005).
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 4592-4593
    • Kimura, M.1    Futamata, M.2    Mukai, R.3    Tamaru, Y.4
  • 14
    • 51349142173 scopus 로고    scopus 로고
    • Fast and highly regioselective allylation of indole and pyrrole compounds by allyl alcohols using Ru-sulfonate catalysts
    • Zaitsev, A. B. et al. Fast and highly regioselective allylation of indole and pyrrole compounds by allyl alcohols using Ru-sulfonate catalysts. J. Am. Chem. Soc. 130, 11604-11605 (2008).
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 11604-11605
    • Zaitsev, A.B.1
  • 15
    • 48849104472 scopus 로고    scopus 로고
    • Ir-catalyzed regio-and enantioselective friedel-crafts-type allylic alkylation of indoles
    • Liu, W., He, H., Dai, L. & You, S. Ir-catalyzed regio-and enantioselective friedel-crafts-type allylic alkylation of indoles. Org. Lett. 10, 1815-1818 (2008).
    • (2008) Org. Lett. , vol.10 , pp. 1815-1818
    • Liu, W.1    He, H.2    Dai, L.3    You, S.4
  • 16
    • 77950478482 scopus 로고    scopus 로고
    • Ruthenium (IV) complexes featuring P, O-chelationg ligands: Regioselective substitution directly from allylic alcohols
    • Sundararaju, B. et al. Ruthenium (IV) complexes featuring P, O-chelationg ligands: Regioselective substitution directly from allylic alcohols. Angew. Chem. Int. Ed. 49, 2782-2785 (2010).
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 2782-2785
    • Sundararaju, B.1
  • 17
    • 84865702897 scopus 로고    scopus 로고
    • Pd(II)-catalyzed regioselective 2-alkylation of indoles via a norbornene-mediated C-H activation: Mechanism and applications
    • Jiao, L., Herdtweck, E. & Bach, T. Pd(II)-catalyzed regioselective 2-alkylation of indoles via a norbornene-mediated C-H activation: Mechanism and applications. J. Am. Chem. Soc. 134, 14563-14572 (2012).
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 14563-14572
    • Jiao, L.1    Herdtweck, E.2    Bach, T.3
  • 18
    • 84873685999 scopus 로고    scopus 로고
    • Iridium-catalyzed intermolecular asymmetric hydroheteroarylation of bicycloalkenes
    • Sevov, C. S. & Hartwig, J. F. Iridium-catalyzed intermolecular asymmetric hydroheteroarylation of bicycloalkenes. J. Am. Chem. Soc. 135, 2116-2119 (2013).
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 2116-2119
    • Sevov, C.S.1    Hartwig, J.F.2
  • 19
    • 0037071923 scopus 로고    scopus 로고
    • Chemo-regio-, and enantioselective Pd-catalyzed allylic alkylation of indolocarbazole pro-aglycons
    • Trost, B. M., Krische, M. J., Berl, V. & Grenzer, E. M. Chemo-, regio-, and enantioselective Pd-catalyzed allylic alkylation of indolocarbazole pro-aglycons. Org. Lett. 4, 2005-2008 (2002).
    • (2002) Org. Lett. , vol.4 , pp. 2005-2008
    • Trost, B.M.1    Krische, M.J.2    Berl, V.3    Grenzer, E.M.4
  • 20
    • 70349783582 scopus 로고    scopus 로고
    • Chemoselective asymmetric N-allylic alkylation of indoles with Morita-Baylis-Hillman carbonates
    • Cui, H. et al. Chemoselective asymmetric N-allylic alkylation of indoles with Morita-Baylis-Hillman carbonates. Angew. Chem. Int. Ed. 48, 5737-5740 (2009).
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 5737-5740
    • Cui, H.1
  • 21
    • 70349925244 scopus 로고    scopus 로고
    • Direct chemoselective N-tert-prenylation of indoles by C-H functionalization
    • Luzung, M. R., Lewis, C. A. & Baran, P. S. Direct, chemoselective N-tert-prenylation of indoles by C-H functionalization. Angew. Chem. Int. Ed. 48, 7025-7029 (2009).
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 7025-7029
    • Luzung, M.R.1    Lewis, C.A.2    Baran, P.S.3
  • 22
    • 70349668803 scopus 로고    scopus 로고
    • Iridium-catalyzed regio-and enantioselective N-allylation of indoles
    • Stanley, L. M. & Hartwig, J. F. Iridium-catalyzed regio-and enantioselective N-allylation of indoles. Angew. Chem. Int. Ed. 48, 7841-7844 (2009).
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 7841-7844
    • Stanley, L.M.1    Hartwig, J.F.2
  • 23
    • 78149258014 scopus 로고    scopus 로고
    • Palladium-catalyzed dynamic kinetic asymmetric transformation of vinyl aziridines with nitrogen heterocycles: Rapid access to biologically active pyrroles and indoles
    • Trost, B. M., Osipov, M. & Dong, G. Palladium-catalyzed dynamic kinetic asymmetric transformation of vinyl aziridines with nitrogen heterocycles: Rapid access to biologically active pyrroles and indoles. J. Am. Chem. Soc. 132, 15800-15807 (2010).
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 15800-15807
    • Trost, B.M.1    Osipov, M.2    Dong, G.3
  • 24
    • 84862106057 scopus 로고    scopus 로고
    • Asymmetric N-allylation of indoles through the iridium-catalyzed allylic alkylation/oxidation of indolines
    • Liu, W., Zhang, X., Dai, L. & You, S. Asymmetric N-allylation of indoles through the iridium-catalyzed allylic alkylation/oxidation of indolines. Angew. Chem. Int. Ed. 51, 5183-5187 (2012).
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 5183-5187
    • Liu, W.1    Zhang, X.2    Dai, L.3    You, S.4
  • 25
    • 33751555599 scopus 로고    scopus 로고
    • Nucleophilic reactivities of indoles
    • Lakhdar, S. et al. Nucleophilic reactivities of indoles. J. Org. Chem. 71, 9088-9095 (2006).
    • (2006) J. Org. Chem. , vol.71 , pp. 9088-9095
    • Lakhdar, S.1
  • 26
    • 34547325807 scopus 로고    scopus 로고
    • Nucleophilicity of indole derivatives: Activating and deactivating effects based on proton affinities and electron density properties
    • Otero, N., Mandado, M. & Mosquera, R. A. Nucleophilicity of indole derivatives: Activating and deactivating effects based on proton affinities and electron density properties. J. Phys. Chem. A 111, 5557-5562 (2007).
    • (2007) J. Phys. Chem. A , vol.111 , pp. 5557-5562
    • Otero, N.1    Mandado, M.2    Mosquera, R.A.3
  • 27
    • 0032496936 scopus 로고    scopus 로고
    • A palladium-catalyzed strategy for the preparation of indoles: A novel entry into the fisher indole synthesis
    • Wagaw, S., Yang, B. H. & Buchwald, S. L. A palladium-catalyzed strategy for the preparation of indoles: A novel entry into the fisher indole synthesis. J. Am. Chem. Soc. 1998 120 6621-6622 (2006).
    • (2006) J. Am. Chem. Soc. , vol.1998 , Issue.120 , pp. 6621-6622
    • Wagaw, S.1    Yang, B.H.2    Buchwald, S.L.3
  • 28
    • 68149176713 scopus 로고    scopus 로고
    • An interrupted fischer indolization approach toward fused indoline-containing natural products
    • Boal, B. W., Schammel, A. W. & Garg, N. K. An interrupted fischer indolization approach toward fused indoline-containing natural products. Org. Lett. 11, 3458-3461 (2009).
    • (2009) Org. Lett. , vol.11 , pp. 3458-3461
    • Boal, B.W.1    Schammel, A.W.2    Garg, N.K.3
  • 29
    • 83055186756 scopus 로고    scopus 로고
    • The catalytic asymmetric fischer indolization
    • Müller, S., Webber, M. J. & List, B. The catalytic asymmetric fischer indolization. J. Am. Chem. Soc. 133, 18534-18537 (2011).
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 18534-18537
    • Müller, S.1    Webber, M.J.2    List, B.3
  • 30
    • 84866041601 scopus 로고    scopus 로고
    • Fischer indole synthesis in low melting mixtures
    • Gore, S., Baskaran, S. & König, B. Fischer indole synthesis in low melting mixtures. Org. Lett. 14, 4568-4571 (2012).
    • (2012) Org. Lett. , vol.14 , pp. 4568-4571
    • Gore, S.1    Baskaran, S.2    König, B.3
  • 31
    • 22244437878 scopus 로고    scopus 로고
    • Acidity of di-and triprotected hydrazine derivatives in dimethyl sulfoxide and aspects of their alkylation
    • Ragnarsson, U. et al. Acidity of di-and triprotected hydrazine derivatives in dimethyl sulfoxide and aspects of their alkylation. J. Org. Chem. 70, 5916-5921 (2005).
    • (2005) J. Org. Chem. , vol.70 , pp. 5916-5921
    • Ragnarsson, U.1
  • 32
    • 33947594333 scopus 로고    scopus 로고
    • Efficient methodology for selective alkylation of hydrazine derivatives
    • Bredihhin, A., Groth, U. M. & Maeörg, U. Efficient methodology for selective alkylation of hydrazine derivatives. Org. Lett. 9, 1097-1099 (2007).
    • (2007) Org. Lett. , vol.9 , pp. 1097-1099
    • Bredihhin, A.1    Groth, U.M.2    Maeörg, U.3
  • 33
    • 34948892781 scopus 로고    scopus 로고
    • Primary tert-and sec-allylamines via palladium-catalyzed hydroamination and allylic substitution with hydrazine and hydroxylamine derivatives
    • Johns, A. M., Liu, Z. & Hartwig, J. F. Primary tert-and sec-allylamines via palladium-catalyzed hydroamination and allylic substitution with hydrazine and hydroxylamine derivatives. Angew. Chem. Int. Ed. 46, 7259-7261 (2007).
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 7259-7261
    • Johns, A.M.1    Liu, Z.2    Hartwig, J.F.3
  • 34
    • 0034245863 scopus 로고    scopus 로고
    • Palladium-catalyzed reactions of allenes
    • Zimmer, R., Dinesh, C., Nandanan, E. & Khan, F. A. Palladium-catalyzed reactions of allenes. Chem. Rev. 100, 3067-3125 (2000).
    • (2000) Chem. Rev. , vol.100 , pp. 3067-3125
    • Zimmer, R.1    Dinesh, C.2    Nandanan, E.3    Khan, F.A.4
  • 35
    • 0347613016 scopus 로고    scopus 로고
    • Palladium-catalyzed asymmetric addition of pronucleophiles to allenes
    • Trost, B. M., Jäkel, C. & Plietker, B. Palladium-catalyzed asymmetric addition of pronucleophiles to allenes. J. Am. Chem. Soc. 125, 4438-4439 (2003).
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 4438-4439
    • Trost, B.M.1    Jäkel, C.2    Plietker, B.3
  • 36
    • 33744546269 scopus 로고    scopus 로고
    • Gold-catalyzed intermolecular hydroamination of allenes with arylamines and resulting high chirality transfer
    • Nishina, N. & Yamamoto, Y. Gold-catalyzed intermolecular hydroamination of allenes with arylamines and resulting high chirality transfer. Angew. Chem. Int. Ed. 45, 3314-3317 (2006).
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 3314-3317
    • Nishina, N.1    Yamamoto, Y.2
  • 37
    • 38949093789 scopus 로고    scopus 로고
    • Iridium-catalyzed hydrocarboxylation of 1, 1-dimethylallene: Byproduct-free reverse prenylation of carboxylic acids
    • Kim, I. S. & Krische, M. J. Iridium-catalyzed hydrocarboxylation of 1, 1-dimethylallene: Byproduct-free reverse prenylation of carboxylic acids. Org. Lett. 10, 513-515 (2006).
    • (2006) Org. Lett. , vol.10 , pp. 513-515
    • Kim, I.S.1    Krische, M.J.2
  • 38
    • 79953101386 scopus 로고    scopus 로고
    • Iridium-catalyzed direct C-C coupling of methanol and allenes
    • Moran, J., Preetz, A., Mesch, R. A. & Krische, M. J. Iridium-catalyzed direct C-C coupling of methanol and allenes. Nat. Chem. 3, 287-290 (2011).
    • (2011) Nat. Chem. , vol.3 , pp. 287-290
    • Moran, J.1    Preetz, A.2    Mesch, R.A.3    Krische, M.J.4
  • 39
    • 84555187000 scopus 로고    scopus 로고
    • Enantioselective synthesis of branched allylic esters via rhodium-catalyzed coupling of allenes with carboxylic acids
    • Koschker, P., Lumbroso, A. & Breit, B. Enantioselective synthesis of branched allylic esters via rhodium-catalyzed coupling of allenes with carboxylic acids. J. Am. Chem. Soc. 133, 20746-20749 (2011).
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 20746-20749
    • Koschker, P.1    Lumbroso, A.2    Breit, B.3
  • 40
    • 84903740004 scopus 로고    scopus 로고
    • Unlocking the N2 selectivity of benzotriazoles: Regiodivergent and highly selective coupling of benzotriazoles with allene
    • Xu, K., Thieme, N. & Breit, B. Unlocking the N2 selectivity of benzotriazoles: Regiodivergent and highly selective coupling of benzotriazoles with allene. Angew. Chem. Int. Ed. 53, 7268-7271 (2014).
    • (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 7268-7271
    • Xu, K.1    Thieme, N.2    Breit, B.3
  • 41
    • 0037060142 scopus 로고    scopus 로고
    • Oxidative addition of N-H bonds to a metal center: Synthesis, characterization, and crystal structure of new rhodium (III) hydrido-pyrazolate complexes
    • Ardizzoia, G. A. et al. Oxidative addition of N-H bonds to a metal center: Synthesis, characterization, and crystal structure of new rhodium (III) hydrido-pyrazolate complexes. Inorg. Chem. 41, 610-614 (2002).
    • (2002) Inorg. Chem. , vol.41 , pp. 610-614
    • Ardizzoia, G.A.1
  • 42
    • 0001208066 scopus 로고    scopus 로고
    • Single and multiple insertion of arylallene into the Rh-H bond to give (p-allyl)rhodium complexes
    • Choi, J., Osakada, K. & Yamamoto, T. Single and multiple insertion of arylallene into the Rh-H bond to give (p-allyl)rhodium complexes. Organometallics 17, 3044-3050 (1998).
    • (1998) Organometallics , vol.17 , pp. 3044-3050
    • Choi, J.1    Osakada, K.2    Yamamoto, T.3
  • 43
    • 84884823602 scopus 로고    scopus 로고
    • Rhodium-catalyzed dynamic kinetic asymmetric transformations of racemic allens by the [32] annulation of aryl ketimines
    • Tran, N. & Cramer, N. Rhodium-catalyzed dynamic kinetic asymmetric transformations of racemic allens by the [32] annulation of aryl ketimines. Angew. Chem. Int. Ed. 52, 10630-10634 (2013).
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 10630-10634
    • Tran, N.1    Cramer, N.2
  • 44
    • 0032503512 scopus 로고    scopus 로고
    • Conservation of absolute configuration in the acyclic rhodium-catalyzed allylic alkylation reaction: Evidence for an enyl (dp) organorhodium intermediate
    • Evans, P. A. & Nelson, J. D. Conservation of absolute configuration in the acyclic rhodium-catalyzed allylic alkylation reaction: Evidence for an enyl (dp) organorhodium intermediate. J. Am. Chem. Soc. 120, 5581-5582 (1998).
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 5581-5582
    • Evans, P.A.1    Nelson, J.D.2
  • 45
    • 70349786223 scopus 로고    scopus 로고
    • First X-ray structure analyses of rhodium(III) Z1-allyl complexes and a mechanism for allylic isomerization reactions
    • Wucher, B., Moser, M., Schumacher, S. A., Rominger, F. & Kunz, D. First X-ray structure analyses of rhodium(III) Z1-allyl complexes and a mechanism for allylic isomerization reactions. Angew. Chem. Int. Ed. 48, 4417-4421 (2009).
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 4417-4421
    • Wucher, B.1    Moser, M.2    Schumacher, S.A.3    Rominger, F.4    Kunz, D.5
  • 46
    • 84893006379 scopus 로고    scopus 로고
    • Mechanistic investigations of the rhodium catalyzed propargylic CH activation
    • Gellrich, U. et al. Mechanistic investigations of the rhodium catalyzed propargylic CH activation. J. Am. Chem. Soc. 136, 1097-1104 (2014).
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 1097-1104
    • Gellrich, U.1


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