메뉴 건너뛰기




Volumn 5, Issue 1, 2011, Pages

A cobalt complex of a microbial arene oxidation product

Author keywords

[No Author keywords available]

Indexed keywords


EID: 82755195792     PISSN: None     EISSN: 1752153X     Source Type: Journal    
DOI: 10.1186/1752-153X-5-80     Document Type: Article
Times cited : (10)

References (56)
  • 1
    • 0014352369 scopus 로고
    • Oxidative degradation of aromatic hydrocarbons by microorganisms. II. Metabolism of halogenated aromatic hydrocarbons
    • Gibson DT, Koch JR, Schuld CL, Kallio RE. Oxidative degradation of aromatic hydrocarbons by microorganisms. II. Metabolism of halogenated aromatic hydrocarbons. Biochem 1968, 7:3795-3802.
    • (1968) Biochem , vol.7 , pp. 3795-3802
    • Gibson, D.T.1    Koch, J.R.2    Schuld, C.L.3    Kallio, R.E.4
  • 2
    • 77956451339 scopus 로고    scopus 로고
    • Recent chemoenzymatic total syntheses of natural and unnatural products: codeine, balanol, pancratistatin, and oseltamivir
    • Hudlický T. Recent chemoenzymatic total syntheses of natural and unnatural products: codeine, balanol, pancratistatin, and oseltamivir. Pure Appl Chem 2010, 82:1785-1796.
    • (2010) Pure Appl Chem , vol.82 , pp. 1785-1796
    • Hudlický, T.1
  • 3
    • 62449130187 scopus 로고    scopus 로고
    • Celebrating 20 years of Synlett - Special account on the merits of biocatalysis and the impact of arene cis-dihydrodiols on enantioselective synthesis
    • Hudlický T, Reed JW. Celebrating 20 years of Synlett - Special account on the merits of biocatalysis and the impact of arene cis-dihydrodiols on enantioselective synthesis. Synlett 2009, 685-703.
    • (2009) Synlett , pp. 685-703
    • Hudlický, T.1    Reed, J.W.2
  • 4
    • 67649381944 scopus 로고    scopus 로고
    • Chemoenzymatic methods for the enantioselective assembly of bioactive natural products
    • Austin KAB, Matveenko M, Reekie TA, Banwell MG. Chemoenzymatic methods for the enantioselective assembly of bioactive natural products. Chem Aust 2008, 75:3-7.
    • (2008) Chem Aust , vol.75 , pp. 3-7
    • Austin, K.A.B.1    Matveenko, M.2    Reekie, T.A.3    Banwell, M.G.4
  • 5
    • 33645677539 scopus 로고    scopus 로고
    • Arene cis-dihydrodiol formation: from biology to application
    • Boyd DR, Bugg TDH. Arene cis-dihydrodiol formation: from biology to application. Org Biomol Chem 2006, 4:181-192.
    • (2006) Org Biomol Chem , vol.4 , pp. 181-192
    • Boyd, D.R.1    Bugg, T.D.H.2
  • 6
    • 5044228492 scopus 로고    scopus 로고
    • Microbial arene oxidations
    • Johnson RA. Microbial arene oxidations. Org React 2004, 63:117-264.
    • (2004) Org React , vol.63 , pp. 117-264
    • Johnson, R.A.1
  • 7
    • 0001846314 scopus 로고    scopus 로고
    • Enzymatic dihydroxylation of aromatics in enantioselective synthesis: expanding asymmetric methodology
    • Hudlický T, Gonzales D, Gibson DT. Enzymatic dihydroxylation of aromatics in enantioselective synthesis: expanding asymmetric methodology. Aldrichimica Acta 1999, 32:35-62.
    • (1999) Aldrichimica Acta , vol.32 , pp. 35-62
    • Hudlický, T.1    Gonzales, D.2    Gibson, D.T.3
  • 8
    • 0002748323 scopus 로고
    • The use of substituted cyclohexadienediols as versatile chiral synthons
    • Widdowson DA, Ribbons DW, Thomas SD. The use of substituted cyclohexadienediols as versatile chiral synthons. Janssen Chimica Acta 1990, 8:3-9.
    • (1990) Janssen Chimica Acta , vol.8 , pp. 3-9
    • Widdowson, D.A.1    Ribbons, D.W.2    Thomas, S.D.3
  • 10
    • 0015236354 scopus 로고
    • Metabolism of benzoic acid by bacteria. Accumulation of (-)-3,5-cyclohexadiene-1,2-diol-1-carboxylic acid by a mutant strain of Alcaligenes eutrophus
    • Reiner AM, Hegeman GD. Metabolism of benzoic acid by bacteria. Accumulation of (-)-3,5-cyclohexadiene-1,2-diol-1-carboxylic acid by a mutant strain of Alcaligenes eutrophus. Biochem 1971, 10:2530-2536.
    • (1971) Biochem , vol.10 , pp. 2530-2536
    • Reiner, A.M.1    Hegeman, G.D.2
  • 11
    • 0022838789 scopus 로고
    • Carbon-13 nuclear magnetic resonance studies in vivo on the metabolism of [1-13C]benzoate by mutants of Pseudomonas putida
    • Cass AEG, Ribbons DW, Rossiter JT, Williams SR. Carbon-13 nuclear magnetic resonance studies in vivo on the metabolism of [1-13C]benzoate by mutants of Pseudomonas putida. Biochem Soc Trans 1986, 14:1268-1269.
    • (1986) Biochem Soc Trans , vol.14 , pp. 1268-1269
    • Cass, A.E.G.1    Ribbons, D.W.2    Rossiter, J.T.3    Williams, S.R.4
  • 12
    • 53249107557 scopus 로고    scopus 로고
    • Microbial production of cis-1,2-dihydroxy-cyclohexa-3,5-diene-1-carboxylate by genetically modified Pseudomonas putida
    • Sun SY, Zhang X, Zhou Q, Chen JC, Chen GQ. Microbial production of cis-1,2-dihydroxy-cyclohexa-3,5-diene-1-carboxylate by genetically modified Pseudomonas putida. Appl Microbiol Biotechnol 2008, 80:977-984.
    • (2008) Appl Microbiol Biotechnol , vol.80 , pp. 977-984
    • Sun, S.Y.1    Zhang, X.2    Zhou, Q.3    Chen, J.C.4    Chen, G.Q.5
  • 13
    • 79955364998 scopus 로고    scopus 로고
    • Expanding the chiral pool: oxidation of meta-bromobenzoic acid by R. eutrophus B9 allows access to new reaction manifolds
    • Griffen JA, le Coz AM, Kociok-Köhn G, Ali Khan M, Stewart AJW, Lewis SE. Expanding the chiral pool: oxidation of meta-bromobenzoic acid by R. eutrophus B9 allows access to new reaction manifolds. Org Biomol Chem 2011, 9:3920-3928.
    • (2011) Org Biomol Chem , vol.9 , pp. 3920-3928
    • Griffen, J.A.1    le Coz, A.M.2    Kociok-Köhn, G.3    Ali Khan, M.4    Stewart, A.J.W.5    Lewis, S.E.6
  • 14
    • 0018830469 scopus 로고
    • Adaptation of Alcaligenes eutrophus B9 and Pseudomonas sp. B13 to 2-fluorobenzoate as growth substrate
    • Engesser KH, Schmidt E, Knackmuss HJ. Adaptation of Alcaligenes eutrophus B9 and Pseudomonas sp. B13 to 2-fluorobenzoate as growth substrate. Appl Environ Microbiol 1980, 39:68-73.
    • (1980) Appl Environ Microbiol , vol.39 , pp. 68-73
    • Engesser, K.H.1    Schmidt, E.2    Knackmuss, H.J.3
  • 15
    • 0001964564 scopus 로고
    • Cis-dihydrodiols microbially produced from halo- and methylbenzoic acids
    • Reineke W, Otting W, Knackmuss HJ. Cis-dihydrodiols microbially produced from halo- and methylbenzoic acids. Tetrahedron 1978, 34:1707-1714.
    • (1978) Tetrahedron , vol.34 , pp. 1707-1714
    • Reineke, W.1    Otting, W.2    Knackmuss, H.J.3
  • 16
    • 0018128525 scopus 로고
    • Chemical structure and biodegradability of halogenated aromatic compounds. Substituent effects on 1,2-dioxygenation of benzoic acid
    • Reineke W, Knackmuss HJ. Chemical structure and biodegradability of halogenated aromatic compounds. Substituent effects on 1,2-dioxygenation of benzoic acid. Biochim Biophys Acta 1978, 542:412-423.
    • (1978) Biochim Biophys Acta , vol.542 , pp. 412-423
    • Reineke, W.1    Knackmuss, H.J.2
  • 17
    • 0015767379 scopus 로고
    • Effect of chloro substituents on the oxygenation of benzoate by Alcaligenes eutrophus B9
    • Knackmuss HJ, Reineke W. Effect of chloro substituents on the oxygenation of benzoate by Alcaligenes eutrophus B9. Chemosphere 1973, 2:225-230.
    • (1973) Chemosphere , vol.2 , pp. 225-230
    • Knackmuss, H.J.1    Reineke, W.2
  • 18
    • 37049066438 scopus 로고
    • Synthetic application of biotransformations: absolute stereochemistry and Diels-Alder reactions of the (1S,2R)-1,2-dihydroxycyclohexa-3,5-diene-1-carboxylic acid from Pseudomonas putida
    • Jenkins GN, Ribbons DW, Widdowson DA, Slawin AMZ, Williams DJ. Synthetic application of biotransformations: absolute stereochemistry and Diels-Alder reactions of the (1S,2R)-1,2-dihydroxycyclohexa-3,5-diene-1-carboxylic acid from Pseudomonas putida. J Chem Soc Perkin Trans 1 1995, 2647-2655.
    • (1995) J Chem Soc Perkin Trans 1 , pp. 2647-2655
    • Jenkins, G.N.1    Ribbons, D.W.2    Widdowson, D.A.3    Slawin, A.M.Z.4    Williams, D.J.5
  • 19
    • 77955772060 scopus 로고    scopus 로고
    • Intramolecular Diels-Alder cyclization of biodihydroxylated benzoic acid derivatives towards novel heterocyclic scaffolds
    • Fischer TCM, Leisch HG, Mihovilovic MD. Intramolecular Diels-Alder cyclization of biodihydroxylated benzoic acid derivatives towards novel heterocyclic scaffolds. Monatsh Chem 2010, 141:699-707.
    • (2010) Monatsh Chem , vol.141 , pp. 699-707
    • Fischer, T.C.M.1    Leisch, H.G.2    Mihovilovic, M.D.3
  • 20
    • 4444356681 scopus 로고    scopus 로고
    • Microwave-mediated intramolecular Diels-Alder cyclization of biodihydroxylated benzoic acid derivatives
    • Mihovilovic MD, Leisch HG, Mereiter K. Microwave-mediated intramolecular Diels-Alder cyclization of biodihydroxylated benzoic acid derivatives. Tetrahedron Lett 2004, 45:7087-7090.
    • (2004) Tetrahedron Lett , vol.45 , pp. 7087-7090
    • Mihovilovic, M.D.1    Leisch, H.G.2    Mereiter, K.3
  • 21
    • 5644245155 scopus 로고    scopus 로고
    • Synthesis of carba-β-L-fructopyranose and carbacyclic analogs of topiramate, an anticonvulsant agent
    • Parker MH, Maryanoff BE, Reitz AB. Synthesis of carba-β-L-fructopyranose and carbacyclic analogs of topiramate, an anticonvulsant agent. Synlett 2004, 2095-2098.
    • (2004) Synlett , pp. 2095-2098
    • Parker, M.H.1    Maryanoff, B.E.2    Reitz, A.B.3
  • 22
    • 79953701655 scopus 로고    scopus 로고
    • "Inosaminoacids": novel inositol-amino acid hybrid structures accessed by microbial arene oxidation
    • Pilgrim S, Kociok-Köhn G, Lloyd MD, Lewis SE. "Inosaminoacids": novel inositol-amino acid hybrid structures accessed by microbial arene oxidation. Chem Commun 2011, 47:4799-4801.
    • (2011) Chem Commun , vol.47 , pp. 4799-4801
    • Pilgrim, S.1    Kociok-Köhn, G.2    Lloyd, M.D.3    Lewis, S.E.4
  • 23
    • 0035818010 scopus 로고    scopus 로고
    • Synthesis of a broad array of highly functionalized, enantiomerically pure cyclohexanecarboxylic acid derivatives by microbial dihydroxylation of benzoic acid and subsequent oxidative and rearrangement reactions
    • Myers AG, Siegel DR, Buzard DJ, Charest MG. Synthesis of a broad array of highly functionalized, enantiomerically pure cyclohexanecarboxylic acid derivatives by microbial dihydroxylation of benzoic acid and subsequent oxidative and rearrangement reactions. Org Lett 2001, 3:2923-2926.
    • (2001) Org Lett , vol.3 , pp. 2923-2926
    • Myers, A.G.1    Siegel, D.R.2    Buzard, D.J.3    Charest, M.G.4
  • 24
    • 17244375099 scopus 로고    scopus 로고
    • A convergent enantioselective route to structurally diverse 6-deoxytetracycline antibiotics
    • Charest MG, Lerner CD, Brubaker JD, Siegel DR, Myers AG. A convergent enantioselective route to structurally diverse 6-deoxytetracycline antibiotics. Science 2005, 308:395-398.
    • (2005) Science , vol.308 , pp. 395-398
    • Charest, M.G.1    Lerner, C.D.2    Brubaker, J.D.3    Siegel, D.R.4    Myers, A.G.5
  • 27
    • 79958806255 scopus 로고    scopus 로고
    • Total synthesis of (+)-grandifloracin by iron complexation of a microbial arene oxidation product
    • Palframan MJ, Kociok-Köhn G, Lewis SE. Total synthesis of (+)-grandifloracin by iron complexation of a microbial arene oxidation product. Org Lett 2011, 13:3150-3153.
    • (2011) Org Lett , vol.13 , pp. 3150-3153
    • Palframan, M.J.1    Kociok-Köhn, G.2    Lewis, S.E.3
  • 28
    • 0038675898 scopus 로고
    • Microbial oxidation in synthesis: preparation of novel 3-substituted cis-cyclohexa-3,5-diene-1,2-diol derivatives from (1S,2S)-3-bromocyclohexa-3,5-diene-1,2-diol
    • Ley SV, Redgrave AJ, Taylor SC, Ahmed S, Ribbons DW. Microbial oxidation in synthesis: preparation of novel 3-substituted cis-cyclohexa-3,5-diene-1,2-diol derivatives from (1S,2S)-3-bromocyclohexa-3,5-diene-1,2-diol. Synlett 1991, 741-742.
    • (1991) Synlett , pp. 741-742
    • Ley, S.V.1    Redgrave, A.J.2    Taylor, S.C.3    Ahmed, S.4    Ribbons, D.W.5
  • 29
    • 0030951756 scopus 로고    scopus 로고
    • New metabolites from toluene dioxygenase dihydroxylation of oxygenated biphenyls
    • Gonzalez D, Schapiro V, Seoane G, Hudlický T. New metabolites from toluene dioxygenase dihydroxylation of oxygenated biphenyls. Tetrahedron: Asymmetry 1997, 8:975-977.
    • (1997) Tetrahedron: Asymmetry , vol.8 , pp. 975-977
    • Gonzalez, D.1    Schapiro, V.2    Seoane, G.3    Hudlický, T.4
  • 30
    • 53849125067 scopus 로고    scopus 로고
    • Diversity-oriented synthesis of enantiomerically pure steroidal tetracycles employing Stille/Diels-Alder reaction sequences
    • Sünnemann HW, Banwell MG, de Meijere A. Diversity-oriented synthesis of enantiomerically pure steroidal tetracycles employing Stille/Diels-Alder reaction sequences. Chem Eur J 2008, 14:7236-7249.
    • (2008) Chem Eur J , vol.14 , pp. 7236-7249
    • Sünnemann, H.W.1    Banwell, M.G.2    de Meijere, A.3
  • 32
    • 0002224233 scopus 로고
    • Transition metal mediated asymmetric synthesis. VII. 6-Methoxycyclohexadienyliron complexes: access to synthetic equivalents of cyclohexadiene dications
    • Howard PW, Stephenson GR, Taylor SC. Transition metal mediated asymmetric synthesis. VII. 6-Methoxycyclohexadienyliron complexes: access to synthetic equivalents of cyclohexadiene dications. J Organomet Chem 1988, 339:C5-C8.
    • (1988) J Organomet Chem , vol.339
    • Howard, P.W.1    Stephenson, G.R.2    Taylor, S.C.3
  • 34
    • 0011620916 scopus 로고
    • Transition metal mediated asymmetric synthesis. X. Homochiral π-complexes with planar chirality: synthetic equivalents of chiral cyclohexadiene dications
    • Howard PW, Stephenson GR, Taylor SC. Transition metal mediated asymmetric synthesis. X. Homochiral π-complexes with planar chirality: synthetic equivalents of chiral cyclohexadiene dications. J Organomet Chem 1989, 370:97-109.
    • (1989) J Organomet Chem , vol.370 , pp. 97-109
    • Howard, P.W.1    Stephenson, G.R.2    Taylor, S.C.3
  • 35
    • 37049071369 scopus 로고
    • Evidence for an anomalous microbial oxidation of acetophenone: new access to optically active tricarbonyliron complexes
    • Howard PW, Stephenson GR, Taylor SC. Evidence for an anomalous microbial oxidation of acetophenone: new access to optically active tricarbonyliron complexes. J Chem Soc Chem Commun 1990, 1182-1184.
    • (1990) J Chem Soc Chem Commun , pp. 1182-1184
    • Howard, P.W.1    Stephenson, G.R.2    Taylor, S.C.3
  • 36
    • 0000793694 scopus 로고
    • Regioselective access to tricarbonyliron complexes: controlled preparation and reactions of trifluoromethyl substituted complexes
    • Howard PW, Stephenson GR, Taylor SC. Regioselective access to tricarbonyliron complexes: controlled preparation and reactions of trifluoromethyl substituted complexes. J Organomet Chem 1991, 419:C14-C17.
    • (1991) J Organomet Chem , vol.419
    • Howard, P.W.1    Stephenson, G.R.2    Taylor, S.C.3
  • 37
    • 37049079698 scopus 로고
    • Assignment of absolute configurations from the circular dichroism spectra of cyclic η4-diene complexes of iron tricarbonyl
    • Stephenson GR, Howard PW, Taylor SC. Assignment of absolute configurations from the circular dichroism spectra of cyclic η4-diene complexes of iron tricarbonyl. J Chem Soc Chem Commun 1991, 127-129.
    • (1991) J Chem Soc Chem Commun , pp. 127-129
    • Stephenson, G.R.1    Howard, P.W.2    Taylor, S.C.3
  • 38
    • 37049071277 scopus 로고
    • Circular dichroism spectra of tricarbonyliron π-complexes
    • Stephenson GR, Howard PW. Circular dichroism spectra of tricarbonyliron π-complexes. J Chem Soc Perkin Trans 1 1994, 2873-2880.
    • (1994) J Chem Soc Perkin Trans 1 , pp. 2873-2880
    • Stephenson, G.R.1    Howard, P.W.2
  • 39
    • 79955411852 scopus 로고    scopus 로고
    • Biphenyl-cis-diol chemistry to access enantiopure aryl-substituted organoiron complexes
    • Stephenson GR, Anson CE, Swinson GJ. Biphenyl-cis-diol chemistry to access enantiopure aryl-substituted organoiron complexes. Tetrahedron Lett 2011, 52:3547-3550.
    • (2011) Tetrahedron Lett , vol.52 , pp. 3547-3550
    • Stephenson, G.R.1    Anson, C.E.2    Swinson, G.J.3
  • 40
    • 0000346419 scopus 로고
    • Preparation of optically pure tricarbonylcyclohexadienyliron complexes: use of a trifluoromethyl group as a regiodirector during hydride abstraction
    • Pearson AJ, Gelormini AM, Pinkerton AA. Preparation of optically pure tricarbonylcyclohexadienyliron complexes: use of a trifluoromethyl group as a regiodirector during hydride abstraction. Organometallics 1992, 11:936-938.
    • (1992) Organometallics , vol.11 , pp. 936-938
    • Pearson, A.J.1    Gelormini, A.M.2    Pinkerton, A.A.3
  • 41
    • 0036027111 scopus 로고    scopus 로고
    • Asymmetric synthesis of C2-symmetric 5,6-bis(benzyloxy)cyclohexa-1,3-diene and a tricarbonyliron complex
    • Watanabe A, Kamahori T, Aso M, Suemune H. Asymmetric synthesis of C2-symmetric 5,6-bis(benzyloxy)cyclohexa-1,3-diene and a tricarbonyliron complex. J Chem Soc Perkin Trans 1 2002, 2539-2543.
    • (2002) J Chem Soc Perkin Trans 1 , pp. 2539-2543
    • Watanabe, A.1    Kamahori, T.2    Aso, M.3    Suemune, H.4
  • 43
    • 0027394827 scopus 로고
    • Hippeastrine synthesis: a combined bio-dioxygenation/organoiron chirality relay approach
    • Astley ST, Meyer M, Stephenson GR. Hippeastrine synthesis: a combined bio-dioxygenation/organoiron chirality relay approach. Tetrahedron Lett 1993, 34:2035-2038.
    • (1993) Tetrahedron Lett , vol.34 , pp. 2035-2038
    • Astley, S.T.1    Meyer, M.2    Stephenson, G.R.3
  • 44
    • 0037010674 scopus 로고    scopus 로고
    • Enzymatic and chemoenzymatic synthesis of arene trans-dihydrodiols
    • Boyd DR, Sharma ND. Enzymatic and chemoenzymatic synthesis of arene trans-dihydrodiols. J Mol Catal B 2002, 19-20:31-42.
    • (2002) J Mol Catal B , vol.19-20 , pp. 31-42
    • Boyd, D.R.1    Sharma, N.D.2
  • 45
    • 73649140240 scopus 로고    scopus 로고
    • Iron(0) tricarbonyl complexes of microbially derived cyclohexadiene ligands containing quaternary stereocentres
    • Ali Khan M, Mahon MF, Stewart AJW, Lewis SE. Iron(0) tricarbonyl complexes of microbially derived cyclohexadiene ligands containing quaternary stereocentres. Organometallics 2010, 29:199-204.
    • (2010) Organometallics , vol.29 , pp. 199-204
    • Ali Khan, M.1    Mahon, M.F.2    Stewart, A.J.W.3    Lewis, S.E.4
  • 46
    • 33847089938 scopus 로고
    • Preparation of the endo-6-acetoxy and endo-6-hydroxy derivatives of η5-(1,3-cyclohexadienyl)iron tricarbonyl fluoroborate
    • Ashworth RW, Berchtold GA. Preparation of the endo-6-acetoxy and endo-6-hydroxy derivatives of η5-(1,3-cyclohexadienyl)iron tricarbonyl fluoroborate. J Am Chem Soc 1977, 99:5200-5201.
    • (1977) J Am Chem Soc , vol.99 , pp. 5200-5201
    • Ashworth, R.W.1    Berchtold, G.A.2
  • 47
    • 0040399097 scopus 로고
    • Comparison of isolobal fragments: bonding of tricarbonyliron and cyclopentadienylcobalt to cyclobutadiene and cyclopentadienone
    • Chinn JW, Hall MB. Comparison of isolobal fragments: bonding of tricarbonyliron and cyclopentadienylcobalt to cyclobutadiene and cyclopentadienone. Organometallics 1984, 3:284-288.
    • (1984) Organometallics , vol.3 , pp. 284-288
    • Chinn, J.W.1    Hall, M.B.2
  • 48
    • 49049145329 scopus 로고
    • Transition metal activation of π-complexed benzene: double nucleophilic additions
    • Lai YH, Tam W, Vollhardt KPC. Transition metal activation of π-complexed benzene: double nucleophilic additions. J Organomet Chem 1981, 216:97-103.
    • (1981) J Organomet Chem , vol.216 , pp. 97-103
    • Lai, Y.H.1    Tam, W.2    Vollhardt, K.P.C.3
  • 49
    • 37049110173 scopus 로고
    • The selective reduction of benzene to cyclohexene mediated by platinum metal complexes: x-ray crystal structure of (2-6-η-1-nitromethylcyclohexadienyl)(1-5-η-pentamethylcyclopentadienyl)iridium(III) tetrafluoroborate
    • Grundy SL, Smith AJ, Adams H, Maitlis PM. The selective reduction of benzene to cyclohexene mediated by platinum metal complexes: x-ray crystal structure of (2-6-η-1-nitromethylcyclohexadienyl)(1-5-η-pentamethylcyclopentadienyl)iridium(III) tetrafluoroborate. J Chem Soc Dalton Trans 1984, 1747-1754.
    • (1984) J Chem Soc Dalton Trans , pp. 1747-1754
    • Grundy, S.L.1    Smith, A.J.2    Adams, H.3    Maitlis, P.M.4
  • 50
    • 84944438568 scopus 로고
    • On enantiomorph-polarity estimation
    • Flack HD. On enantiomorph-polarity estimation. Acta Cryst 1983, A39:876-881.
    • (1983) Acta Cryst , vol.A39 , pp. 876-881
    • Flack, H.D.1
  • 51
    • 78649819135 scopus 로고    scopus 로고
    • Accessing the antipodal series in microbial arene oxidation: a novel diene rearrangement induced by tricarbonyliron(0) complexation
    • Ali Khan M, Lowe JP, Johnson AL, Stewart AJW, Lewis SE. Accessing the antipodal series in microbial arene oxidation: a novel diene rearrangement induced by tricarbonyliron(0) complexation. Chem Commun 2011, 47:215-217.
    • (2011) Chem Commun , vol.47 , pp. 215-217
    • Ali Khan, M.1    Lowe, J.P.2    Johnson, A.L.3    Stewart, A.J.W.4    Lewis, S.E.5
  • 52
    • 0000723362 scopus 로고
    • An unprecedented propellane-to-spirofused skeletal rearrangement upon oxidative demetalation of cyclopentadienyl cobalt-complexed polycyclic dienes: synthesis of a pentacyclic, potential precursor to strychnine
    • Grotjahn DB, Vollhardt KPC. An unprecedented propellane-to-spirofused skeletal rearrangement upon oxidative demetalation of cyclopentadienyl cobalt-complexed polycyclic dienes: synthesis of a pentacyclic, potential precursor to strychnine. J Am Chem Soc 1990, 112:5653-5654.
    • (1990) J Am Chem Soc , vol.112 , pp. 5653-5654
    • Grotjahn, D.B.1    Vollhardt, K.P.C.2
  • 53
    • 0000420509 scopus 로고
    • [2+2+2] Cycloadditions of alkynes to furans and thiophenes: A cobalt-mediated "enol ether walk"
    • Boese R, Harvey DF, Malaska MJ, Vollhardt KPC. [2+2+2] Cycloadditions of alkynes to furans and thiophenes: A cobalt-mediated "enol ether walk". J Am Chem Soc 1994, 116:11153-11154.
    • (1994) J Am Chem Soc , vol.116 , pp. 11153-11154
    • Boese, R.1    Harvey, D.F.2    Malaska, M.J.3    Vollhardt, K.P.C.4
  • 54
    • 0034632432 scopus 로고    scopus 로고
    • The formal total synthesis of (±)-strychnine via a cobalt-mediated [2+2+2] cycloaddition
    • Eichberg MJ, Dorta RL, Lamottke K, Vollhardt KPC. The formal total synthesis of (±)-strychnine via a cobalt-mediated [2+2+2] cycloaddition. Org Lett 2000, 2:2479-2481.
    • (2000) Org Lett , vol.2 , pp. 2479-2481
    • Eichberg, M.J.1    Dorta, R.L.2    Lamottke, K.3    Vollhardt, K.P.C.4
  • 55
    • 0035955025 scopus 로고    scopus 로고
    • Approaches to the synthesis of (±)-strychnine via the cobalt-mediated [2+2+2] cycloaddition: rapid assembly of a classic framework
    • Eichberg MJ, Dorta RL, Grotjahn DB, Lamottke K, Schmidt M, Vollhardt KPC. Approaches to the synthesis of (±)-strychnine via the cobalt-mediated [2+2+2] cycloaddition: rapid assembly of a classic framework. J Am Chem Soc 2001, 123:9324-9337.
    • (2001) J Am Chem Soc , vol.123 , pp. 9324-9337
    • Eichberg, M.J.1    Dorta, R.L.2    Grotjahn, D.B.3    Lamottke, K.4    Schmidt, M.5    Vollhardt, K.P.C.6
  • 56
    • 0000114230 scopus 로고
    • Synthese und reaktionen von η5-cyclopentadienylbis(ethen)cobalt
    • Jonas K, Deffense E, Habermann D. Synthese und reaktionen von η5-cyclopentadienylbis(ethen)cobalt. Angew Chem 1983, 95:729.
    • (1983) Angew Chem , vol.95 , pp. 729
    • Jonas, K.1    Deffense, E.2    Habermann, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.