메뉴 건너뛰기




Volumn 7, Issue , 2016, Pages

Radical aryl migration enables diversity-oriented synthesis of structurally diverse medium/macro- or bridged-rings

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE DERIVATIVE; AMINE; BRIDGED COMPOUND; CARBON; HETEROCYCLIC KETONE; ALKENE; KETONE; MACROCYCLIC COMPOUND;

EID: 85006955818     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms13852     Document Type: Article
Times cited : (159)

References (54)
  • 1
    • 84862008385 scopus 로고    scopus 로고
    • Diversity-oriented synthesis: Producing chemical tools for dissecting biology
    • O Connor, C. J., Beckmann, H. S. G. and Spring, D. R. Diversity-oriented synthesis: producing chemical tools for dissecting biology. Chem. Soc. Rev. 41, 4444-4456 (2012).
    • (2012) Chem. Soc. Rev. , vol.41 , pp. 4444-4456
    • Connor, C.J.O.1    Beckmann, H.S.G.2    Spring, D.R.3
  • 2
    • 33644839988 scopus 로고    scopus 로고
    • Diversity-oriented synthesis: Exploring the intersections between chemistry and biology
    • Tan, D. S. Diversity-oriented synthesis: exploring the intersections between chemistry and biology. Nat. Chem. Biol. 1, 74-84 (2005).
    • (2005) Nat. Chem. Biol. , vol.1 , pp. 74-84
    • Tan, D.S.1
  • 3
    • 84880296641 scopus 로고    scopus 로고
    • Diversity-oriented synthesis as a tool for the discovery of novel biologically active small molecules
    • Galloway, W. R. J. D., Isidro-Llobet, A. and Spring, D. R. Diversity-oriented synthesis as a tool for the discovery of novel biologically active small molecules. Nat. Commun. 1, 80 (2010).
    • (2010) Nat. Commun. , vol.1 , pp. 80
    • Galloway, W.R.J.D.1    Isidro-Llobet, A.2    Spring, D.R.3
  • 5
    • 0010571757 scopus 로고
    • Total synthesis of (+-)-byssochlamic acid
    • Stork, G., Tabak, J. M. and Blount, J. F. Total synthesis of (+-)-byssochlamic acid. J. Am. Chem. Soc. 94, 4735-4737 (1972).
    • (1972) J. Am. Chem. Soc. , vol.94 , pp. 4735-4737
    • Stork, G.1    Tabak, J.M.2    Blount, J.F.3
  • 6
    • 34249903067 scopus 로고    scopus 로고
    • Natural products with maleic anhydride structure: Nonadrides, tautomycin, chaetomellic anhydride, and other compounds
    • Chen, X., Zheng, Y. and Shen, Y. Natural products with maleic anhydride structure: nonadrides, tautomycin, chaetomellic anhydride, and other compounds. Chem. Rev. 107, 1777-1830 (2007).
    • (2007) Chem. Rev. , vol.107 , pp. 1777-1830
    • Chen, X.1    Zheng, Y.2    Shen, Y.3
  • 7
    • 33748480130 scopus 로고    scopus 로고
    • A convergent and enantioselective synthesis of (+)-amurensinine via selective C-H and C-C bond insertion reactions
    • Tambar, U. K., Ebner, D. C. and Stoltz, B. M. A convergent and enantioselective synthesis of (+)-amurensinine via selective C-H and C-C bond insertion reactions. J. Am. Chem. Soc. 128, 11752-11753 (2006).
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 11752-11753
    • Tambar, U.K.1    Ebner, D.C.2    Stoltz, B.M.3
  • 8
    • 0037413546 scopus 로고    scopus 로고
    • The power of visual imagery in drug design. Isopavines as a new class of morphinomimetics and their human opioid receptor binding activity
    • Hanessian, S., Parthasarathy, S. and Mauduit, M. The power of visual imagery in drug design. Isopavines as a new class of morphinomimetics and their human opioid receptor binding activity. J. Med. Chem. 46, 34-48 (2003).
    • (2003) J. Med. Chem. , vol.46 , pp. 34-48
    • Hanessian, S.1    Parthasarathy, S.2    Mauduit, M.3
  • 9
    • 84861187385 scopus 로고    scopus 로고
    • Bio-inspired synthesis and biological evaluation of a colchicine-related compound library
    • Nicolaou, K. C., Valiulin, R. A., Pokorski, J. K., Chang, V. and Chen, J. S. Bio-inspired synthesis and biological evaluation of a colchicine-related compound library. Bioorg. Med. Chem. Lett. 22, 3776-3780 (2012).
    • (2012) Bioorg. Med. Chem. Lett. , vol.22 , pp. 3776-3780
    • Nicolaou, K.C.1    Valiulin, R.A.2    Pokorski, J.K.3    Chang, V.4    Chen, J.S.5
  • 10
    • 78650122737 scopus 로고    scopus 로고
    • A graphical journey of innovative organic architectures that have improved our lives
    • McGrath, N. A., Brichacek, M. and Njardarson, J. T. A graphical journey of innovative organic architectures that have improved our lives. J. Chem. Educ. 87, 1348-1349 (2010).
    • (2010) J. Chem. Educ. , vol.87 , pp. 1348-1349
    • McGrath, N.A.1    Brichacek, M.2    Njardarson, J.T.3
  • 11
    • 33846870797 scopus 로고    scopus 로고
    • Total synthesis of natural 8- and 9-membered lactones: Recent advancements in medium-sized ring formation
    • Shiina, I. Total synthesis of natural 8- and 9-membered lactones: recent advancements in medium-sized ring formation. Chem. Rev. 107, 239-273 (2007).
    • (2007) Chem. Rev. , vol.107 , pp. 239-273
    • Shiina, I.1
  • 12
    • 84863393865 scopus 로고    scopus 로고
    • Microwave-assisted synthesis of medium-sized heterocycles
    • Sharma, A., Appukkuttan, P. and Van der Eycken, E. Microwave-assisted synthesis of medium-sized heterocycles. Chem. Commun. 48, 1623-1637 (2012).
    • (2012) Chem. Commun. , vol.48 , pp. 1623-1637
    • Sharma, A.1    Appukkuttan, P.2    Van Der Eycken, E.3
  • 13
    • 84872253105 scopus 로고    scopus 로고
    • Update 1 of: Macrolactonizations in the total synthesis of natural products
    • Parenty, A., Moreau, X., Niel, G. and Campagne, J.-M. Update 1 of: Macrolactonizations in the total synthesis of natural products. Chem. Rev 113, PR1-PR40 (2013).
    • (2013) Chem. Rev , vol.113 , pp. PR1-PR40
    • Parenty, A.1    Moreau, X.2    Niel, G.3    Campagne, J.-M.4
  • 15
    • 0027521367 scopus 로고
    • Syntheses of medium sized rings by ring expansion reactions
    • Roxburgh, C. J. Syntheses of medium sized rings by ring expansion reactions. Tetrahedron 49, 10749-10784 (1993).
    • (1993) Tetrahedron , vol.49 , pp. 10749-10784
    • Roxburgh, C.J.1
  • 17
    • 84862667189 scopus 로고    scopus 로고
    • Synthesis of eight-membered lactones: Intermolecular [6+2] cyclization of amphoteric molecules with siloxy alkynes
    • Zhao, W.-X., Wang, Z.-B. and Sun, J.-W. Synthesis of eight-membered lactones: intermolecular [6+2] cyclization of amphoteric molecules with siloxy alkynes. Angew. Chem. Int. Ed. 51, 6209-6213 (2012).
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 6209-6213
    • Zhao, W.-X.1    Wang, Z.-B.2    Sun, J.-W.3
  • 18
    • 84871342809 scopus 로고    scopus 로고
    • Biomimetic diversity-oriented synthesis of benzannulated medium rings via ring expansion
    • Bauer, R. A., Wenderski, T. A. and Tan, D. S. Biomimetic diversity-oriented synthesis of benzannulated medium rings via ring expansion. Nat. Chem. Biol. 9, 21-29 (2013).
    • (2013) Nat. Chem. Biol. , vol.9 , pp. 21-29
    • Bauer, R.A.1    Wenderski, T.A.2    Tan, D.S.3
  • 19
    • 84925251578 scopus 로고    scopus 로고
    • Silver-catalyzed ring-opening strategy for the synthesis of b- and g-fluorinated ketones
    • Zhao, H., Fan, X., Yu, J. and Zhu, C. Silver-catalyzed ring-opening strategy for the synthesis of b- and g-fluorinated ketones. J. Am. Chem. Soc. 137, 3490-3493 (2015).
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 3490-3493
    • Zhao, H.1    Fan, X.2    Yu, J.3    Zhu, C.4
  • 22
    • 0035955789 scopus 로고    scopus 로고
    • Radical aryl migration reactions
    • Studer, A. and Bossart, M. Radical aryl migration reactions. Tetrahedron 57, 9649-9667 (2001).
    • (2001) Tetrahedron , vol.57 , pp. 9649-9667
    • Studer, A.1    Bossart, M.2
  • 23
    • 84937468844 scopus 로고    scopus 로고
    • Radical aryl migration reactions and synthetic applications
    • Chen, Z.-M., Zhang, X.-M. and Tu, Y.-Q. Radical aryl migration reactions and synthetic applications. Chem. Soc. Rev. 44, 5220-5245 (2015).
    • (2015) Chem. Soc. Rev. , vol.44 , pp. 5220-5245
    • Chen, Z.-M.1    Zhang, X.-M.2    Tu, Y.-Q.3
  • 24
    • 84904467583 scopus 로고    scopus 로고
    • Copper-catalyzed one-pot trifluoromethylation/aryl migration/ carbonyl formation with homopropargylic alcohols
    • Gao, P. et al. Copper-catalyzed one-pot trifluoromethylation/aryl migration/ carbonyl formation with homopropargylic alcohols. Angew. Chem. Int. Ed. 53, 7629-7633 (2014).
    • (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 7629-7633
    • Gao, P.1
  • 25
    • 84948660254 scopus 로고    scopus 로고
    • Silver-catalyzed long-distance aryl migration from carbon center to nitrogen center
    • Zhou, T.-G., Luo, F.-X., Yang, M.-Y. and Shi, Z.-J. Silver-catalyzed long-distance aryl migration from carbon center to nitrogen center. J. Am. Chem. Soc. 137, 14586-14589 (2015).
    • (2015) J. Am. Chem. Soc. , vol.137 , pp. 14586-14589
    • Zhou, T.-G.1    Luo, F.-X.2    Yang, M.-Y.3    Shi, Z.-J.4
  • 26
    • 84885144334 scopus 로고    scopus 로고
    • Copper-catalyzed one-pot trifluoromethylation/aryl migration/desulfonylation and C(sp2)-N bond formation of conjugated tosyl amides
    • Kong, W., Casimiro, M., Merino, E. and Nevado, C. Copper-catalyzed one-pot trifluoromethylation/aryl migration/desulfonylation and C(sp2)-N bond formation of conjugated tosyl amides. J. Am. Chem. Soc. 135, 14480-14483 (2013).
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 14480-14483
    • Kong, W.1    Casimiro, M.2    Merino, E.3    Nevado, C.4
  • 28
    • 84900026201 scopus 로고    scopus 로고
    • Arylphosphonylation and arylazidation of activated alkenes
    • Kong, W., Merino, E. and Nevado, C. Arylphosphonylation and arylazidation of activated alkenes. Angew. Chem. Int. Ed. 53, 5078-5082 (2014).
    • (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 5078-5082
    • Kong, W.1    Merino, E.2    Nevado, C.3
  • 29
    • 84954350178 scopus 로고    scopus 로고
    • Recent advances in the one-step synthesis of distally fluorinated ketones
    • Zeng, Y., Ni, C. and Hu, J. Recent advances in the one-step synthesis of distally fluorinated ketones. Chem. Eur. J. 22, 3210-3223 (2016).
    • (2016) Chem. Eur. J. , vol.22 , pp. 3210-3223
    • Zeng, Y.1    Ni, C.2    Hu, J.3
  • 30
    • 84883545162 scopus 로고    scopus 로고
    • Copper-catalyzed tandem trifluoromethylation/semipinacol rearrangement of allylic alcohols
    • Chen, Z.-M. et al. Copper-catalyzed tandem trifluoromethylation/semipinacol rearrangement of allylic alcohols. Angew. Chem. Int. Ed. 52, 9781-9785 (2013).
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 9781-9785
    • Chen, Z.-M.1
  • 31
    • 85027934449 scopus 로고    scopus 로고
    • Copper-catalyzed cyanomethylation of allylic alcohols with concomitant 1,2-aryl migration: Efficient synthesis of functionalized ketones containing an a-quaternary center
    • Bunescu, A., Wang, Q. and Zhu, J. Copper-catalyzed cyanomethylation of allylic alcohols with concomitant 1,2-aryl migration: efficient synthesis of functionalized ketones containing an a-quaternary center. Angew. Chem. Int. Ed. 54, 3132-3135 (2015).
    • (2015) Angew. Chem. Int. Ed. , vol.54 , pp. 3132-3135
    • Bunescu, A.1    Wang, Q.2    Zhu, J.3
  • 32
    • 84919398837 scopus 로고    scopus 로고
    • Enantioselective C-H bond functionalization triggered by radical trifluoromethylation of unactivated alkene
    • Yu, P. et al. Enantioselective C-H bond functionalization triggered by radical trifluoromethylation of unactivated alkene. Angew. Chem. Int. Ed. 53, 11890-11894 (2014).
    • (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 11890-11894
    • Yu, P.1
  • 33
    • 84924905328 scopus 로고    scopus 로고
    • Phosphine-catalyzed remote b-C-H functionalization of amines triggered by trifluoromethylation of alkenes: One-pot synthesis of bistrifluoromethylated enamides and oxazoles
    • Yu, P., Zheng, S.-C., Yang, N.-Y., Tan, B. and Liu, X.-Y. Phosphine-catalyzed remote b-C-H functionalization of amines triggered by trifluoromethylation of alkenes: one-pot synthesis of bistrifluoromethylated enamides and oxazoles. Angew. Chem. Int. Ed. 54, 4041-4045 (2015).
    • (2015) Angew. Chem. Int. Ed. , vol.54 , pp. 4041-4045
    • Yu, P.1    Zheng, S.-C.2    Yang, N.-Y.3    Tan, B.4    Liu, X.-Y.5
  • 34
    • 84983551223 scopus 로고    scopus 로고
    • Combination of a cyano migration strategy and alkene difunctionalization: The elusive selective azidocyanation of unactivated olefins
    • Wu, Z., Ren, R. and Zhu, C. Combination of a cyano migration strategy and alkene difunctionalization: the elusive selective azidocyanation of unactivated olefins. Angew. Chem. Int. Ed. 55, 10821-10824 (2016).
    • (2016) Angew. Chem. Int. Ed. , vol.55 , pp. 10821-10824
    • Wu, Z.1    Ren, R.2    Zhu, C.3
  • 35
    • 84921791732 scopus 로고    scopus 로고
    • Electrophilic trifluoromethylation by use of hypervalent iodine reagents
    • Charpentier, J., Fruh, N. and Togni, A. Electrophilic trifluoromethylation by use of hypervalent iodine reagents. Chem. Rev. 115, 650-682 (2015).
    • (2015) Chem. Rev. , vol.115 , pp. 650-682
    • Charpentier, J.1    Fruh, N.2    Togni, A.3
  • 36
    • 84906534625 scopus 로고    scopus 로고
    • The electron is a catalyst
    • Studer, A. and Curran, D. P. The electron is a catalyst. Nat. Chem. 6, 765-773 (2014).
    • (2014) Nat. Chem. , vol.6 , pp. 765-773
    • Studer, A.1    Curran, D.P.2
  • 37
    • 84864443774 scopus 로고    scopus 로고
    • Copper-catalyzed oxytrifluoromethylation of unactivated alkenes
    • Zhu, R. and Buchwald, S. L. Copper-catalyzed oxytrifluoromethylation of unactivated alkenes. J. Am. Chem. Soc. 134, 12462-12465 (2012).
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 12462-12465
    • Zhu, R.1    Buchwald, S.L.2
  • 38
    • 84890584717 scopus 로고    scopus 로고
    • Copper-catalyzed three-component oxytrifluoromethylation of alkenes with sodium trifluoromethanesulfinate and hydroxamic acid
    • Jiang, X.-Y. and Qing, F.-L. Copper-catalyzed three-component oxytrifluoromethylation of alkenes with sodium trifluoromethanesulfinate and hydroxamic acid. Angew. Chem. Int. Ed. 52, 14177-14180 (2013).
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 14177-14180
    • Jiang, X.-Y.1    Qing, F.-L.2
  • 39
    • 84883885666 scopus 로고    scopus 로고
    • Chemistry of bridged lactams and related heterocycles
    • Szostak, M. and Aube, J. Chemistry of bridged lactams and related heterocycles. Chem. Rev. 113, 5701-5765 (2013).
    • (2013) Chem. Rev. , vol.113 , pp. 5701-5765
    • Szostak, M.1    Aube, J.2
  • 40
    • 84904812553 scopus 로고    scopus 로고
    • Cooperative activation of cyclobutanones and olefins leads to bridged ring systems by a catalytic [4+2] coupling
    • Ko, H. M. and Dong, G. Cooperative activation of cyclobutanones and olefins leads to bridged ring systems by a catalytic [4+2] coupling. Nat. Chem. 6, 739-744 (2014).
    • (2014) Nat. Chem. , vol.6 , pp. 739-744
    • Ko, H.M.1    Dong, G.2
  • 41
    • 84870530501 scopus 로고    scopus 로고
    • Vinyl and alkynyl azides: Well-known intermediates in the focus of modern synthetic methods
    • Jung, N. and Brase, S. Vinyl and alkynyl azides: well-known intermediates in the focus of modern synthetic methods. Angew. Chem. Int. Ed. 51, 12169-12171 (2013).
    • (2013) Angew. Chem. Int. Ed. , vol.51 , pp. 12169-12171
    • Jung, N.1    Brase, S.2
  • 42
    • 84879335245 scopus 로고    scopus 로고
    • Site-selective catalytic C(sp2)-H bond azidations
    • Song, W., Kozhushkov, S. I. and Ackermann, L. Site-selective catalytic C(sp2)-H bond azidations. Angew. Chem. Int. Ed. 52, 6576-6578 (2013).
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 6576-6578
    • Song, W.1    Kozhushkov, S.I.2    Ackermann, L.3
  • 43
    • 0029898398 scopus 로고    scopus 로고
    • Preparation, X-ray crystal structure, and chemistry of stable azidoiodinanes derivatives of benziodoxole
    • Zhdankin, V. V. et al. Preparation, X-ray crystal structure, and chemistry of stable azidoiodinanes derivatives of benziodoxole. J. Am. Chem. Soc. 118, 5192-5197 (1996).
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 5192-5197
    • Zhdankin, V.V.1
  • 44
    • 34848848499 scopus 로고    scopus 로고
    • Fluorine in pharmaceuticals: Looking beyond intuition
    • Muller, K., Faeh, C. and Diederich, F. Fluorine in pharmaceuticals: looking beyond intuition. Science 317, 1881-1886 (2007).
    • (2007) Science , vol.317 , pp. 1881-1886
    • Muller, K.1    Faeh, C.2    Diederich, F.3
  • 45
    • 79957603696 scopus 로고    scopus 로고
    • Metal-catalysed cross-coupling reactions
    • Furuya, T., Kamlet, A. S. and Ritter, T. Metal-catalysed cross-coupling reactions. Nature 473, 470-477 (2011).
    • (2011) Nature , vol.473 , pp. 470-477
    • Furuya, T.1    Kamlet, A.S.2    Ritter, T.3
  • 46
    • 33644919105 scopus 로고    scopus 로고
    • Novel 10-I-3 hypervalent iodine-based compounds for electrophilic trifluoromethylation
    • Eisenberger, P., Gischig, S. and Togni, A. Novel 10-I-3 hypervalent iodine-based compounds for electrophilic trifluoromethylation. Chem. Eur. J. 12, 2579-2586 (2006).
    • (2006) Chem. Eur. J. , vol.12 , pp. 2579-2586
    • Eisenberger, P.1    Gischig, S.2    Togni, A.3
  • 47
    • 0034647763 scopus 로고    scopus 로고
    • Stereoselective radical aryl migration from silicon to carbon
    • Amrein, S., Bossart, M., Vasella, T. and Studer, A. Stereoselective radical aryl migration from silicon to carbon. J. Org. Chem. 65, 4281-4288 (2000).
    • (2000) J. Org. Chem. , vol.65 , pp. 4281-4288
    • Amrein, S.1    Bossart, M.2    Vasella, T.3    Studer, A.4
  • 48
    • 84884178706 scopus 로고    scopus 로고
    • Asymmetric a-arylation of amino acid derivatives by clayden rearrangement of ester enolates via memory of chirality
    • Tomohara, K., Yoshimura, T., Hyakutake, R., Yang, P. and Kawabata, T. Asymmetric a-arylation of amino acid derivatives by clayden rearrangement of ester enolates via memory of chirality. J. Am. Chem. Soc. 135, 13294-13297 (2013).
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 13294-13297
    • Tomohara, K.1    Yoshimura, T.2    Hyakutake, R.3    Yang, P.4    Kawabata, T.5
  • 49
    • 77951699144 scopus 로고    scopus 로고
    • Computational explorations of mechanisms and ligand-directed selectivities of copper-catalyzed Ullmanntype reactions
    • Jones, G. O., Liu, P., Houk, K. N. and Buchwald, S. L. Computational explorations of mechanisms and ligand-directed selectivities of copper-catalyzed Ullmanntype reactions. J. Am. Chem. Soc. 132, 6205-6213 (2010).
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 6205-6213
    • Jones, G.O.1    Liu, P.2    Houk, K.N.3    Buchwald, S.L.4
  • 50
    • 78650628456 scopus 로고    scopus 로고
    • Alternative mechanistic explanation for ligand-dependent selectivities in copper-catalyzed N- and O-arylation reactions
    • Yu, H.-Z., Jiang, Y.-Y., Fu, Y. and Liu, L. Alternative mechanistic explanation for ligand-dependent selectivities in copper-catalyzed N- and O-arylation reactions. J. Am. Chem. Soc. 132, 18078-18091 (2010).
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 18078-18091
    • Yu, H.-Z.1    Jiang, Y.-Y.2    Fu, Y.3    Liu, L.4
  • 51
    • 33744981391 scopus 로고    scopus 로고
    • Synthesis and structural analysis of 2-quinuclidonium tetrafluoroborate
    • Tani, K. and Stoltz, B. M. Synthesis and structural analysis of 2-quinuclidonium tetrafluoroborate. Nature 441, 731-734 (2006).
    • (2006) Nature , vol.441 , pp. 731-734
    • Tani, K.1    Stoltz, B.M.2
  • 52
    • 0001183472 scopus 로고
    • Intramolecular schmidt reactions of alkyl azides with ketones: Scope and stereochemical studies
    • Milligan, G. L., Mossman, C. J. and Aubé, J. Intramolecular schmidt reactions of alkyl azides with ketones: scope and stereochemical studies. J. Am. Chem. Soc. 117, 10449-10459 (1995).
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 10449-10459
    • Milligan, G.L.1    Mossman, C.J.2    Aubé, J.3
  • 53
    • 84883866387 scopus 로고    scopus 로고
    • Recent advances in organocatalytic asymmetric morita- baylis-hillman/aza-morita-baylis-hillman reactions
    • Wei, Y. and Shi, M. Recent advances in organocatalytic asymmetric morita- baylis-hillman/aza-morita-baylis-hillman reactions. Chem. Rev. 113, 6659-6690 (2013).
    • (2013) Chem. Rev. , vol.113 , pp. 6659-6690
    • Wei, Y.1    Shi, M.2
  • 54
    • 0034246704 scopus 로고    scopus 로고
    • Metal-mediated synthesis of medium-sized rings
    • Yet, L. Metal-mediated synthesis of medium-sized rings. Chem. Rev. 100, 2963-3008 (2000).
    • (2000) Chem. Rev. , vol.100 , pp. 2963-3008
    • Yet, L.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.