메뉴 건너뛰기




Volumn 5, Issue , 2014, Pages

Intramolecular C-F and C-H bond cleavage promoted by butadienyl heavy Grignard reagents

Author keywords

[No Author keywords available]

Indexed keywords

ALKENYL GROUP; GRIGNARD REAGENT; IODIDE; NAPHTHALENE DERIVATIVE;

EID: 84918553443     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms5508     Document Type: Article
Times cited : (46)

References (57)
  • 1
    • 64549085877 scopus 로고    scopus 로고
    • The Grignard reagents
    • Seyferth, D. The Grignard reagents. Organometallics 28, 1598-1605 (2009).
    • (2009) Organometallics , vol.28 , pp. 1598-1605
    • Seyferth, D.1
  • 2
    • 0034520691 scopus 로고    scopus 로고
    • Non-cyclopentadienyl organometallic compounds of calcium, strontium and barium
    • Hanusa, T. P. Non-cyclopentadienyl organometallic compounds of calcium, strontium and barium. Coord. Chem. Rev. 210, 329-367 (2000).
    • (2000) Coord. Chem. Rev. , vol.210 , pp. 329-367
    • Hanusa, T.P.1
  • 3
    • 0036840125 scopus 로고    scopus 로고
    • Not Just heavy "Grignards": Recent advances in the organometallic chemistry of the alkaline earth metals calcium, strontium and barium
    • Alexander, J. S. & Ruhlandt-Senge, K. Not Just heavy "Grignards": recent advances in the organometallic chemistry of the alkaline earth metals calcium, strontium and barium. Eur. J. Inorg. Chem. 2002, 2761-2774 (2002).
    • (2002) Eur. J. Inorg. Chem. , vol.2002 , pp. 2761-2774
    • Alexander, J.S.1    Ruhlandt-Senge, K.2
  • 4
    • 34250820510 scopus 로고    scopus 로고
    • Aryl calcium compounds: Syntheses, structures, physical properties, and chemical behavior
    • Westerhausen, M., Gärtner, M., Fischer, R. & Langer, J. Aryl calcium compounds: syntheses, structures, physical properties, and chemical behavior. Angew. Chem. Int. Ed. 46, 1950-1956 (2007).
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 1950-1956
    • Westerhausen, M.1    Gärtner, M.2    Fischer, R.3    Langer, J.4
  • 5
    • 44649181502 scopus 로고    scopus 로고
    • Heavy Grignard reagents-synthesis and reactivity of organocalcium compounds
    • Westerhausen, M. Heavy Grignard reagents-synthesis and reactivity of organocalcium compounds. Coord. Chem. Rev. 252, 1516-1531 (2008).
    • (2008) Coord. Chem. Rev. , vol.252 , pp. 1516-1531
    • Westerhausen, M.1
  • 6
    • 70349941238 scopus 로고    scopus 로고
    • Organometallic compounds of the heavier s-block elements-What next?
    • Smith, J. D. Organometallic compounds of the heavier s-block elements-What next? Angew. Chem. Int. Ed. 48, 6597-6599 (2009).
    • (2009) Angew. Chem. Int. Ed , vol.48 , pp. 6597-6599
    • Smith, J.D.1
  • 7
    • 79954587057 scopus 로고    scopus 로고
    • Geminal dianions stabilized by phosphonium substituents
    • Harder, S. Geminal dianions stabilized by phosphonium substituents. Coord. Chem. Rev. 255, 1252-1267 (2011).
    • (2011) Coord. Chem. Rev. , vol.255 , pp. 1252-1267
    • Harder, S.1
  • 8
    • 0035898512 scopus 로고    scopus 로고
    • Barium triphenylmethanide: An examination of anion basicity
    • Alexander, J. S. & Ruhlandt-Senge, K. Barium triphenylmethanide: an examination of anion basicity. Angew. Chem. Int. Ed. 40, 2658-2660 (2001).
    • (2001) Angew. Chem. Int. Ed , vol.40 , pp. 2658-2660
    • Alexander, J.S.1    Ruhlandt-Senge, K.2
  • 9
    • 0000718158 scopus 로고
    • Organocalcium chemistry: Preparation and reactions of highly reactive calcium
    • Wu, T.-C., Xiong, H. & Rieke, R. D. Organocalcium chemistry: preparation and reactions of highly reactive calcium. J. Org. Chem. 55, 5045-5051 (1990).
    • (1990) J. Org. Chem. , vol.55 , pp. 5045-5051
    • Wu, T.-C.1    Xiong, H.2    Rieke, R.D.3
  • 10
    • 0000058830 scopus 로고
    • Allylbarium reagents: Unprecedented regio- and stereoselective allylation reactions of carbonyl compounds
    • Yanagisawa, A., Habaue, S., Yasue, K. & Yamamoto, H. Allylbarium reagents: unprecedented regio- and stereoselective allylation reactions of carbonyl compounds. J. Am. Chem. Soc. 116, 6130-6141 (1994).
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 6130-6141
    • Yanagisawa, A.1    Habaue, S.2    Yasue, K.3    Yamamoto, H.4
  • 11
    • 1642295771 scopus 로고    scopus 로고
    • Reactive barium-promoted reformatsky-type reaction of α-chloroketones with aldehydes
    • Yanagisawa, A., Takahashi, H. & Arai, T. Reactive barium-promoted reformatsky-type reaction of α-chloroketones with aldehydes. Chem. Commun. 580-581 (2004).
    • (2004) Chem. Commun. , pp. 580-581
    • Yanagisawa, A.1    Takahashi, H.2    Arai, T.3
  • 12
    • 54549089927 scopus 로고    scopus 로고
    • Selective propargylation of carbonyl compounds and imines with barium reagents
    • Yanagisawa, A., Suzuki, T., Koide, T., Okitsu, S. & Arai, T. Selective propargylation of carbonyl compounds and imines with barium reagents. Chem. Asian J. 3, 1793-1800 (2008).
    • (2008) Chem. Asian J , vol.3 , pp. 1793-1800
    • Yanagisawa, A.1    Suzuki, T.2    Koide, T.3    Okitsu, S.4    Arai, T.5
  • 13
    • 0032527712 scopus 로고    scopus 로고
    • A unique barium-carbon bond: Mechanism of formation and crystallographic characterization
    • Westerhausen, M., Digeser, M. H., Nöth, H., Seifert, T. & Pfitzner, A. A unique barium-carbon bond: mechanism of formation and crystallographic characterization. J. Am. Chem. Soc. 120, 6722-6725 (1998).
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 6722-6725
    • Westerhausen, M.1    Digeser, M.H.2    Nöth, H.3    Seifert, T.4    Pfitzner, A.5
  • 14
    • 0000998391 scopus 로고    scopus 로고
    • 2,5-Diphenyl-3,4-bis(trimethylsilyl)-1-phosphacyclopentadienide as a ligand at calcium, strontium and tin(II)
    • Westerhausen, M. et al. 2,5-diphenyl-3,4-bis(trimethylsilyl)-1-phosphacyclopentadienide as a ligand at calcium, strontium and tin(II). Inorg. Chem. 38, 3207-3214 (1999).
    • (1999) Inorg. Chem. , vol.38 , pp. 3207-3214
    • Westerhausen, M.1
  • 17
    • 34248145917 scopus 로고    scopus 로고
    • THF solvates of extremely soluble bis(2,4,6-trimethylphenyl)calcium and tris(2,6-dimethoxyphenyl)-dicalcium iodide
    • Fischer, R. et al. THF solvates of extremely soluble bis(2,4,6-trimethylphenyl)calcium and tris(2,6-dimethoxyphenyl)-dicalcium iodide. Angew. Chem. Int. Ed. 46, 1618-1623 (2007).
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 1618-1623
    • Fischer, R.1
  • 18
    • 84893781386 scopus 로고    scopus 로고
    • Arylcalcium halides as substrates in Kumada-type cross-coupling reactions
    • Langer, J., Köhler, M., Görls, H. & Westerhausen, M. Arylcalcium halides as substrates in Kumada-type cross-coupling reactions. J. Organomet. Chem. 751, 563-567 (2014).
    • (2014) J. Organomet. Chem. , vol.751 , pp. 563-567
    • Langer, J.1    Köhler, M.2    Görls, H.3    Westerhausen, M.4
  • 19
    • 0039183328 scopus 로고
    • Preparation of organometallic compounds from highly reactive metal powders
    • Rieke, R. D. Preparation of organometallic compounds from highly reactive metal powders. Science 246, 1260-1264 (1989).
    • (1989) Science , vol.246 , pp. 1260-1264
    • Rieke, R.D.1
  • 20
    • 77955577152 scopus 로고    scopus 로고
    • Synthesis and reaction of dibenzo[a,e]pentalene
    • Saito, M. Synthesis and reaction of dibenzo[a,e]pentalene. Symmetry 2, 950-969 (2010).
    • (2010) Symmetry , vol.2 , pp. 950-969
    • Saito, M.1
  • 21
    • 84887538972 scopus 로고    scopus 로고
    • Pentalenes-From highly reactive antiaromatics to substrates for material science
    • Hopf, H. Pentalenes-From highly reactive antiaromatics to substrates for material science. Angew. Chem. Int. Ed. 52, 12224-12226 (2013).
    • (2013) Angew. Chem. Int. Ed , vol.52 , pp. 12224-12226
    • Hopf, H.1
  • 22
    • 34250711880 scopus 로고    scopus 로고
    • Reduction of phenyl silyl acetylenes with lithium: Unexpected formation of a dilithium dibenzopentalenide
    • Saito, M., Nakamura, M., Tajima, T. & Yoshioka, M. Reduction of phenyl silyl acetylenes with lithium: unexpected formation of a dilithium dibenzopentalenide. Angew. Chem. Int. Ed. 46, 1504-1507 (2007).
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 1504-1507
    • Saito, M.1    Nakamura, M.2    Tajima, T.3    Yoshioka, M.4
  • 23
    • 67749145474 scopus 로고    scopus 로고
    • Versatile synthesis of pentalene derivatives via the Pd-catalyzed homocoupling of haloenynes
    • Levi, Z. U. & Tilley, T. D. Versatile synthesis of pentalene derivatives via the Pd-catalyzed homocoupling of haloenynes. J. Am. Chem. Soc. 131, 2796-2797 (2009).
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 2796-2797
    • Levi, Z.U.1    Tilley, T.D.2
  • 24
    • 84864625512 scopus 로고    scopus 로고
    • Dihalo-substituted dibenzopentalenes: Their practical synthesis and transformation to dibenzopentalene derivatives
    • Xu, F., Peng, L., Orita, A. & Otera, J. Dihalo-substituted dibenzopentalenes: their practical synthesis and transformation to dibenzopentalene derivatives. Org. Lett. 14, 3970-3973 (2012).
    • (2012) Org. Lett. , vol.14 , pp. 3970-3973
    • Xu, F.1    Peng, L.2    Orita, A.3    Otera, J.4
  • 25
    • 84858022319 scopus 로고    scopus 로고
    • Gold-catalyzed synthesis of dibenzopentalenes-Evidence for gold vinylidenes
    • Hashmi, A. S. K. et al. Gold-catalyzed synthesis of dibenzopentalenes-Evidence for gold vinylidenes. Adv. Synth. Catal. 354, 555-562 (2012).
    • (2012) Adv. Synth. Catal , vol.354 , pp. 555-562
    • Hashmi, A.S.K.1
  • 27
    • 84878384741 scopus 로고    scopus 로고
    • 3-induced cyclization reactions of 1,2-bis(phenylethynyl)benzenes
    • 3-induced cyclization reactions of 1,2-bis(phenylethynyl)benzenes. Angew. Chem. Int. Ed. 52, 5992-5996 (2013).
    • (2013) Angew. Chem. Int. Ed , vol.52 , pp. 5992-5996
    • Chen, C.1
  • 28
    • 84880391045 scopus 로고    scopus 로고
    • Pd-catalyzed cascade crossover annulation of o-alkynylarylhalides and diarylacetylenes leading to dibenzo[a,e]pentalenes
    • Zhao, J., Oniwa, K., Asao, N., Yamamoto, Y. & Jin, T. Pd-catalyzed cascade crossover annulation of o-alkynylarylhalides and diarylacetylenes leading to dibenzo[a,e]pentalenes. J. Am. Chem. Soc. 135, 10222-10225 (2013).
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 10222-10225
    • Zhao, J.1    Oniwa, K.2    Asao, N.3    Yamamoto, Y.4    Jin, T.5
  • 29
    • 84881097669 scopus 로고    scopus 로고
    • Stabilization of anti-aromatic and strained five-membered rings with a transition metal
    • Zhu, C. et al. Stabilization of anti-aromatic and strained five-membered rings with a transition metal. Nat. Chem. 5, 698-703 (2013).
    • (2013) Nat. Chem. , vol.5 , pp. 698-703
    • Zhu, C.1
  • 30
    • 84893445494 scopus 로고    scopus 로고
    • Pentalenes with novel topologies: Exploiting the cascade carbopalladation reaction between alkynes and gem-dibromoolefins
    • London, G. et al. Pentalenes with novel topologies: exploiting the cascade carbopalladation reaction between alkynes and gem-dibromoolefins. Chem. Sci. 5, 965-972 (2014).
    • (2014) Chem. Sci. , vol.5 , pp. 965-972
    • London, G.1
  • 31
    • 78249246805 scopus 로고    scopus 로고
    • Dinaphthopentalenes: Pentalene derivatives for organic thin-film transistors
    • Kawase, T. et al. Dinaphthopentalenes: pentalene derivatives for organic thin-film transistors. Angew. Chem. Int. Ed. 49, 7728-7732 (2010).
    • (2010) Angew. Chem. Int. Ed , vol.49 , pp. 7728-7732
    • Kawase, T.1
  • 32
    • 0041914506 scopus 로고    scopus 로고
    • Building blocks for n-type organic electronics: Regiochemically modulated inversion of majority carrier sign in perfluoroarene-modified polythiophene semiconductors
    • Facchetti, A. et al. Building blocks for n-type organic electronics: regiochemically modulated inversion of majority carrier sign in perfluoroarene-modified polythiophene semiconductors. Angew. Chem. Int. Ed. 42, 3900-3903 (2003).
    • (2003) Angew. Chem. Int. Ed , vol.42 , pp. 3900-3903
    • Facchetti, A.1
  • 33
    • 3042811341 scopus 로고    scopus 로고
    • Perfluoropentacene: High-performance p-n junctions and complementary circuits with pentacene
    • Sakamoto, Y. et al. Perfluoropentacene: high-performance p-n junctions and complementary circuits with pentacene. J. Am. Chem. Soc. 126, 8138-8140 (2004).
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 8138-8140
    • Sakamoto, Y.1
  • 35
    • 66249097754 scopus 로고    scopus 로고
    • C-F bond activation in organic synthesis
    • Amii, H. & Uneyama, K. C-F bond activation in organic synthesis. Chem. Rev. 109, 2119-2183 (2009).
    • (2009) Chem. Rev. , vol.109 , pp. 2119-2183
    • Amii, H.1    Uneyama, K.2
  • 36
    • 79956212759 scopus 로고    scopus 로고
    • C-F and C-H bond activation of fluorobenzenes and fluoropyridines at transition metal centers: How fluorine tips the scales
    • Clot, E. et al. C-F and C-H bond activation of fluorobenzenes and fluoropyridines at transition metal centers: how fluorine tips the scales. Acc. Chem. Res. 44, 333-348 (2011).
    • (2011) Acc. Chem. Res. , vol.44 , pp. 333-348
    • Clot, E.1
  • 37
    • 84879986986 scopus 로고    scopus 로고
    • Main-group Lewis acids for C-F bond activaton
    • Stahl, T., Klare, H. F. T. & Oestreich, M. Main-group Lewis acids for C-F bond activaton. ACS Catal. 3, 1578-1587 (2013).
    • (2013) ACS Catal , vol.3 , pp. 1578-1587
    • Stahl, T.1    Klare, H.F.T.2    Oestreich, M.3
  • 38
    • 0343907171 scopus 로고    scopus 로고
    • Remarkable effect of copper chloride on diiodination of zirconacyclopentadienes
    • Xi, C., Huo, S., Afifi, T. H., Hara, R. & Takahashi, T. Remarkable effect of copper chloride on diiodination of zirconacyclopentadienes. Tetrahedron Lett. 38, 4099-4102 (1997).
    • (1997) Tetrahedron Lett. , vol.38 , pp. 4099-4102
    • Xi, C.1    Huo, S.2    Afifi, T.H.3    Hara, R.4    Takahashi, T.5
  • 39
    • 0037427254 scopus 로고    scopus 로고
    • Regioselective coupling of pentafluorophenyl substituted alkynes: Mechanistic insight into the zirconocene coupling of alkynes and a facile route to conjugated polymers bearing electron-withdrawing pentafluorophenyl substituents
    • Johnson, S. A. et al. Regioselective coupling of pentafluorophenyl substituted alkynes: mechanistic insight into the zirconocene coupling of alkynes and a facile route to conjugated polymers bearing electron-withdrawing pentafluorophenyl substituents. J. Am. Chem. Soc. 125, 4199-4211 (2003).
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 4199-4211
    • Johnson, S.A.1
  • 40
    • 24944478226 scopus 로고    scopus 로고
    • Stabilization of aryl-calcium, -strontium, and -barium compounds by designed steric and π-bonding encapsulation
    • Hauber, S.-O., Lissner, F., Deacon, G. B. & Niemeyer, M. Stabilization of aryl-calcium, -strontium, and -barium compounds by designed steric and π-bonding encapsulation. Angew. Chem. Int. Ed. 44, 5871-5875 (2005).
    • (2005) Angew. Chem. Int. Ed , vol.44 , pp. 5871-5875
    • Hauber, S.-O.1    Lissner, F.2    Deacon, G.B.3    Niemeyer, M.4
  • 41
    • 33847804589 scopus 로고
    • Activated Metals. IV. Preparation and reactions of highly reactive magnesium metal
    • Rieke, R. D. & Bales, S. E. Activated Metals. IV. Preparation and reactions of highly reactive magnesium metal. J. Am. Chem. Soc. 96, 1775-1781 (1974).
    • (1974) J. Am. Chem. Soc. , vol.96 , pp. 1775-1781
    • Rieke, R.D.1    Bales, S.E.2
  • 42
    • 81255178349 scopus 로고    scopus 로고
    • Electron-accepting 6,12-diethynylindeno[1,2-b]fluorenes: Synthesis, crystal structures, and photophysical properties
    • Chase, D. T. et al. Electron-accepting 6,12-diethynylindeno[1,2-b]fluorenes: synthesis, crystal structures, and photophysical properties. Angew. Chem. Int. Ed. 50, 11103-11106 (2011).
    • (2011) Angew. Chem. Int. Ed , vol.50 , pp. 11103-11106
    • Chase, D.T.1
  • 43
    • 0037124841 scopus 로고    scopus 로고
    • A highly regioselective synthesis of polysubstituted naphthalene derivatives through gallium trichloride catalyzed alkyne-aldehyde coupling
    • Viswanathan, G. S., Wang, M. & Li, C.-J. A highly regioselective synthesis of polysubstituted naphthalene derivatives through gallium trichloride catalyzed alkyne-aldehyde coupling. Angew. Chem. Int. Ed. 41, 2138-2141 (2002).
    • (2002) Angew. Chem. Int. Ed , vol.41 , pp. 2138-2141
    • Viswanathan, G.S.1    Wang, M.2    Li, C.-J.3
  • 44
    • 0141542714 scopus 로고    scopus 로고
    • A new titanium tetrachloride mediated annulation of α-aryl-substituted carbonyl compounds with alkynes: A simple and highly efficient method for the regioselective synthesis of polysubstituted naphthalene derivatives
    • Kabalka, G. W., Ju, Y. & Wu, Z. A new titanium tetrachloride mediated annulation of α-aryl-substituted carbonyl compounds with alkynes: a simple and highly efficient method for the regioselective synthesis of polysubstituted naphthalene derivatives. J. Org. Chem. 68, 7915-7917 (2003).
    • (2003) J. Org. Chem. , vol.68 , pp. 7915-7917
    • Kabalka, G.W.1    Ju, Y.2    Wu, Z.3
  • 45
    • 0034598514 scopus 로고    scopus 로고
    • Palladium-catalyzed intermolecular controlled insertion of benzyne-benzyne-alkene and benzyne-alkyne-alkene-Synthesis of phenanthrene and naphthalene derivatives
    • Yoshikawa, E. & Yamamoto, Y. Palladium-catalyzed intermolecular controlled insertion of benzyne-benzyne-alkene and benzyne-alkyne-alkene-Synthesis of phenanthrene and naphthalene derivatives. Angew. Chem. Int. Ed. 39, 173-175 (2000).
    • (2000) Angew. Chem. Int. Ed , vol.39 , pp. 173-175
    • Yoshikawa, E.1    Yamamoto, Y.2
  • 46
    • 77955679627 scopus 로고    scopus 로고
    • Sulfur-assisted propargyl-allenyl isomerizations and electrocyclizations for the convenient and efficient synthesis of polyfunctionalized benzenes and naphthalenes
    • Zhou, H., Xing, Y., Yao, J. & Chen, J. Sulfur-assisted propargyl-allenyl isomerizations and electrocyclizations for the convenient and efficient synthesis of polyfunctionalized benzenes and naphthalenes. Org. Lett. 12, 3674-3677 (2010).
    • (2010) Org. Lett. , vol.12 , pp. 3674-3677
    • Zhou, H.1    Xing, Y.2    Yao, J.3    Chen, J.4
  • 47
    • 78650262767 scopus 로고    scopus 로고
    • Palladium-catalyzed bisolefination of C-C triple bonds: A facile method for the synthesis of naphthalene derivatives
    • Feng, C. & Loh, T.-P. Palladium-catalyzed bisolefination of C-C triple bonds: a facile method for the synthesis of naphthalene derivatives. J. Am. Chem. Soc. 132, 17710-17712 (2010).
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 17710-17712
    • Feng, C.1    Loh, T.-P.2
  • 48
    • 84982074638 scopus 로고
    • Der konformative ortho-effekt bei o-tolylstilbenen und deren vinyllithiumderivaten
    • Knorr, R., Lattke, E. & Räpple, E. Der konformative ortho-effekt bei o-tolylstilbenen und deren vinyllithiumderivaten. Chem. Ber. 114, 1581-1591 (1981).
    • (1981) Chem. Ber , vol.114 , pp. 1581-1591
    • Knorr, R.1    Lattke, E.2    Räpple, E.3
  • 49
    • 31044441850 scopus 로고    scopus 로고
    • Synthesis of 2,4,6-trimethylphenylcalcium iodide and degradation in THF solution
    • Fischer, R., Gärtner, M., Görls, H. & Westerhausen, M. Synthesis of 2,4,6-trimethylphenylcalcium iodide and degradation in THF solution. Angew. Chem. Int. Ed. 45, 609-612 (2006).
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 609-612
    • Fischer, R.1    Gärtner, M.2    Görls, H.3    Westerhausen, M.4
  • 50
  • 51
    • 0000127170 scopus 로고    scopus 로고
    • The phosphonium dibenzylide anion as a ligand in organobarium chemistry
    • Harder, S. & Lutz, M. The phosphonium dibenzylide anion as a ligand in organobarium chemistry. Organometallics 16, 225-230 (1997).
    • (1997) Organometallics , vol.16 , pp. 225-230
    • Harder, S.1    Lutz, M.2
  • 52
    • 0035809966 scopus 로고    scopus 로고
    • Synthesis of strontium and barium bis{tris[(trimethylsilyl)methyl]zincates} via the transmetalation of bis[(trimethylsilyl)methyl]zinc
    • Westerhausen, M. et al. Synthesis of strontium and barium bis{tris[(trimethylsilyl)methyl]zincates} via the transmetalation of bis[(trimethylsilyl)methyl]zinc. Organometallics 20, 893-899 (2001).
    • (2001) Organometallics , vol.20 , pp. 893-899
    • Westerhausen, M.1
  • 53
    • 84896901955 scopus 로고    scopus 로고
    • Structural evidence of strong calcium-π interactions to aryl substituents stabilized by coexistent agostic bonds to alkyl groups
    • Loh, C., Seupel, S., Görls, H., Krieck, S. & Westerhausen, M. Structural evidence of strong calcium-π interactions to aryl substituents stabilized by coexistent agostic bonds to alkyl groups. Organometallics 33, 1480-1491 (2014).
    • (2014) Organometallics , vol.33 , pp. 1480-1491
    • Loh, C.1    Seupel, S.2    Görls, H.3    Krieck, S.4    Westerhausen, M.5
  • 55
    • 37549039510 scopus 로고    scopus 로고
    • A short history of SHELX
    • Sheldrick, G. M. A short history of SHELX. Acta Cryst. A64, 112-122 (2008).
    • (2008) Acta Cryst , vol.A64 , pp. 112-122
    • Sheldrick, G.M.1
  • 56
    • 33646767009 scopus 로고    scopus 로고
    • ORTEP-3 for Windows - A version of ORTEP-III with a Graphical User Interface (GUI)
    • Farrugia, L. J. ORTEP-3 for Windows - a version of ORTEP-III with a Graphical User Interface (GUI). J. Appl. Cryst. 30, 565-566 (1997).
    • (1997) J. Appl. Cryst , vol.30 , pp. 565-566
    • Farrugia, L.J.1
  • 57
    • 70450206724 scopus 로고    scopus 로고
    • Revision B.01 Gaussian, Inc.
    • Frisch, M. J. et al. Gaussian 09. Revision B.01 (Gaussian, Inc., 2010).
    • (2010) Gaussian 09
    • Frisch, M.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.