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Volumn 6, Issue , 2015, Pages

Total synthesis of clostrubin

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBIOTIC AGENT; CLOSTRUBIN; UNCLASSIFIED DRUG; ALKENE; ANTIINFECTIVE AGENT; POLYCYCLIC AROMATIC HYDROCARBON; POLYKETIDE; POLYPHENOL;

EID: 84924794981     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms7445     Document Type: Article
Times cited : (50)

References (70)
  • 1
    • 0036682463 scopus 로고    scopus 로고
    • 'Superbug' hurdles key drug barrier
    • Pearson, H. 'Superbug' hurdles key drug barrier. Nature 418, 469-469 (2002).
    • (2002) Nature , vol.418 , pp. 469-469
    • Pearson, H.1
  • 2
    • 84887627398 scopus 로고    scopus 로고
    • Antibiotic resistance - The need for global solutions
    • Laxminarayan, R. et al. Antibiotic resistance - the need for global solutions. Lancet Infect. Dis. 13, 1057-1058 (2013).
    • (2013) Lancet Infect. Dis. , vol.13 , pp. 1057-1058
    • Laxminarayan, R.1
  • 3
    • 33845708150 scopus 로고    scopus 로고
    • New antibiotics from bacterial natural products
    • Clardy, J., Fischbach, M. A. & Walsh, C. T. New antibiotics from bacterial natural products. Nat. Biotechnol. 24, 1541-1550 (2006).
    • (2006) Nat. Biotechnol. , vol.24 , pp. 1541-1550
    • Clardy, J.1    Fischbach, M.A.2    Walsh, C.T.3
  • 4
    • 69549111337 scopus 로고    scopus 로고
    • Antibiotics for emerging pathogens
    • Fischbach, M. A. & Walsh, C. T. Antibiotics for emerging pathogens. Science 325, 1089-1093 (2009).
    • (2009) Science , vol.325 , pp. 1089-1093
    • Fischbach, M.A.1    Walsh, C.T.2
  • 5
    • 33749030702 scopus 로고    scopus 로고
    • Platensimycin, a new antibiotic and "superbug challenger" from nature
    • Häbich, D. & von Nussbaum, F. Platensimycin, a new antibiotic and "superbug challenger" from nature. ChemMedChem 1, 951-954 (2006).
    • (2006) ChemMedChem , vol.1 , pp. 951-954
    • Häbich, D.1    Von Nussbaum, F.2
  • 9
    • 14844340653 scopus 로고    scopus 로고
    • Chemistry and biology of ramoplanin: A lipoglycodepsipeptide with potent antibiotic activity
    • Walker, S. et al. Chemistry and biology of ramoplanin: a lipoglycodepsipeptide with potent antibiotic activity. Chem. Rev. 105, 449-476 (2005).
    • (2005) Chem. Rev. , vol.105 , pp. 449-476
    • Walker, S.1
  • 10
  • 11
    • 34247606516 scopus 로고    scopus 로고
    • Structure and total synthesis of lysobactin (katanosin B)
    • von Nussbaum, F. et al. Structure and total synthesis of lysobactin (katanosin B). Angew. Chem. Int. Ed. 46, 2039-2042 (2007).
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 2039-2042
    • Von Nussbaum, F.1
  • 12
    • 84864342971 scopus 로고    scopus 로고
    • Latent antibiotics and the potential of the arylomycins for broad-spectrum antibacterial activity
    • Tan, Y. X. & Romesberg, F. E. Latent antibiotics and the potential of the arylomycins for broad-spectrum antibacterial activity. Med. Chem. Commun. 3, 916-925 (2012).
    • (2012) Med. Chem. Commun. , vol.3 , pp. 916-925
    • Tan, Y.X.1    Romesberg, F.E.2
  • 13
    • 84876726616 scopus 로고    scopus 로고
    • Total synthesis of daptomycin by cyclization via a chemoselective serine ligation
    • Lam, H. Y. et al. Total synthesis of daptomycin by cyclization via a chemoselective serine ligation. J. Am. Chem. Soc. 135, 6272-6279 (2013).
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 6272-6279
    • Lam, H.Y.1
  • 14
    • 84903457328 scopus 로고    scopus 로고
    • Aspergillomarasmine A overcomes metallo-β-lactamase antibiotic resistance
    • King, A. M. et al. Aspergillomarasmine A overcomes metallo-β-lactamase antibiotic resistance. Nature 510, 503-506 (2014).
    • (2014) Nature , vol.510 , pp. 503-506
    • King, A.M.1
  • 15
    • 84904562314 scopus 로고    scopus 로고
    • Discovery of clostrubin, an exceptional polyphenolic polyketide antibiotic from a strictly anaerobic bacterium
    • Pidot, S., Ishida, K., Cyrulies, M. & Hertweck, C. Discovery of clostrubin, an exceptional polyphenolic polyketide antibiotic from a strictly anaerobic bacterium. Angew. Chem. Int. Ed. 53, 7856-7859 (2014).
    • (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 7856-7859
    • Pidot, S.1    Ishida, K.2    Cyrulies, M.3    Hertweck, C.4
  • 16
    • 0035803049 scopus 로고    scopus 로고
    • Total synthesis of variolin B
    • Anderson, R. J. & Morris, J. C. Total synthesis of variolin B. Tetrahedron Lett. 42, 8697-8699 (2001).
    • (2001) Tetrahedron Lett , vol.42 , pp. 8697-8699
    • Anderson, R.J.1    Morris, J.C.2
  • 17
    • 0000635846 scopus 로고
    • The endiandric acid cascade. Electrocyclizations in organic synthesis. 1. Stepwise, stereocontrolled total synthesis of endiandric acids A and B
    • Nicolaou, K. C., Petasis, N. A., Zipkin, R. E. & Uenishi, J. The endiandric acid cascade. Electrocyclizations in organic synthesis. 1. Stepwise, stereocontrolled total synthesis of endiandric acids A and B. J. Am. Chem. Soc. 104, 5555-5557 (1982).
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 5555-5557
    • Nicolaou, K.C.1    Petasis, N.A.2    Zipkin, R.E.3    Uenishi, J.4
  • 18
    • 0000454836 scopus 로고
    • The endiandric acid cascade. Electrocyclizations in organic synthesis. 2. Stepwise, stereocontrolled total synthesis of endiandric acids C-G
    • Nicolaou, K. C., Petasis, N. A., Uenishi, J. & Zipkin, R. E. The endiandric acid cascade. Electrocyclizations in organic synthesis. 2. Stepwise, stereocontrolled total synthesis of endiandric acids C-G. J. Am. Chem. Soc. 104, 5557-5558 (1982).
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 5557-5558
    • Nicolaou, K.C.1    Petasis, N.A.2    Uenishi, J.3    Zipkin, R.E.4
  • 19
    • 0000510718 scopus 로고
    • The endiandric acid cascade. Electrocyclizations in organic synthesis. 3. "Biomimetic" approach to endiandric acids A-G. Synthesis of precursors
    • Nicolaou, K. C., Zipkin, R. E. & Petasis, N. A. The endiandric acid cascade. Electrocyclizations in organic synthesis. 3. "Biomimetic" approach to endiandric acids A-G. Synthesis of precursors. J. Am. Chem. Soc. 104, 5558-5560 (1982).
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 5558-5560
    • Nicolaou, K.C.1    Zipkin, R.E.2    Petasis, N.A.3
  • 20
    • 0001225884 scopus 로고
    • The endiandric acid cascade. Electrocyclizations in organic synthesis. 4. Biomimetic approach to endiandric acids A-G. Total synthesis and thermal studies
    • Nicolaou, K. C., Petasis, N. A. & Zipkin, R. E. The endiandric acid cascade. Electrocyclizations in organic synthesis. 4. Biomimetic approach to endiandric acids A-G. Total synthesis and thermal studies. J. Am. Chem. Soc. 104, 5560-5562 (1982).
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 5560-5562
    • Nicolaou, K.C.1    Petasis, N.A.2    Zipkin, R.E.3
  • 21
    • 30744456247 scopus 로고    scopus 로고
    • Biosynthetic and biomimetic electrocyclizations
    • Beaudry, C. M., Malerich, J. P. & Trauner, D. Biosynthetic and biomimetic electrocyclizations. Chem. Rev. 105, 4757-4778 (2005).
    • (2005) Chem. Rev. , vol.105 , pp. 4757-4778
    • Beaudry, C.M.1    Malerich, J.P.2    Trauner, D.3
  • 22
    • 0037019536 scopus 로고    scopus 로고
    • Stereoselective formal [3 + 3] cycloaddition approach to cis-1-azadecalins and synthesis of (-)-4a,8a-diepi-pumiliotoxin C. Evidence for the first highly stereoselective 6π-electron electrocyclic ring closures of 1-azatrienes
    • Sklenicka, H. M. et al. Stereoselective formal [3 + 3] cycloaddition approach to cis-1-azadecalins and synthesis of (-)-4a,8a-diepi-pumiliotoxin C. Evidence for the first highly stereoselective 6π-electron electrocyclic ring closures of 1-azatrienes. J. Am. Chem. Soc. 124, 10435-10442 (2002).
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 10435-10442
    • Sklenicka, H.M.1
  • 23
    • 0242416942 scopus 로고    scopus 로고
    • Total synthesis of the quinone epoxide dimer (+)-torreyanic acid: Application of a biomimetic oxidation/electrocyclization/Diels-Alder dimerization cascade
    • Li, C., Johnson, R. P. & Porco, J. A. Total synthesis of the quinone epoxide dimer (+)-torreyanic acid: application of a biomimetic oxidation/electrocyclization/Diels-Alder dimerization cascade. J. Am. Chem. Soc. 125, 5095-5106 (2003).
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 5095-5106
    • Li, C.1    Johnson, R.P.2    Porco, J.A.3
  • 24
    • 10344248926 scopus 로고    scopus 로고
    • The Total synthesis of (-)-SNF4435 C and (+)-SNF4435 D
    • Parker, K. A. & Lim, Y.-H. The Total synthesis of (-)-SNF4435 C and (+)-SNF4435 D. J. Am. Chem. Soc. 126, 15968-15969 (2004).
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 15968-15969
    • Parker, K.A.1    Lim, Y.-H.2
  • 25
    • 22744446475 scopus 로고    scopus 로고
    • Mining the tetraene manifold: Total synthesis of complex pyrones from Placobranchus ocellatus
    • Miller, A. K. & Trauner, D. Mining the tetraene manifold: total synthesis of complex pyrones from Placobranchus ocellatus. Angew. Chem. Int. Ed. 44, 4602-4606 (2005).
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 4602-4606
    • Miller, A.K.1    Trauner, D.2
  • 26
    • 49949089657 scopus 로고    scopus 로고
    • Biomimetic synthesis of the IDO inhibitors exiguamine A and B
    • Volgraf, M. et al. Biomimetic synthesis of the IDO inhibitors exiguamine A and B. Nat. Chem. Biol. 4, 535-537 (2008).
    • (2008) Nat. Chem. Biol. , vol.4 , pp. 535-537
    • Volgraf, M.1
  • 27
    • 58249124539 scopus 로고    scopus 로고
    • 3)-H activation/electrocyclization strategy: Total synthesis of coralydine
    • 3)-H activation/electrocyclization strategy: total synthesis of coralydine. Angew. Chem. Int. Ed. 48, 179-182 (2009).
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 179-182
    • Chaumontet, M.1    Piccardi, R.2    Baudoin, O.3
  • 28
    • 79959864466 scopus 로고    scopus 로고
    • Total synthesis and absolute stereochemical assignment of kibdelone C
    • Sloman, D. L., Bacon, J. W. & Porco, J. A. Total synthesis and absolute stereochemical assignment of kibdelone C. J. Am. Chem. Soc. 133, 9952-9955 (2011).
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 9952-9955
    • Sloman, D.L.1    Bacon, J.W.2    Porco, J.A.3
  • 29
    • 80052946499 scopus 로고    scopus 로고
    • A synthetic approach to kingianin A based on biosynthetic speculation
    • Sharma, P., Ritson, D. J., Burnley, J. & Moses, J. E. A synthetic approach to kingianin A based on biosynthetic speculation. Chem. Commun. 47, 10605-10607 (2011).
    • (2011) Chem. Commun. , vol.47 , pp. 10605-10607
    • Sharma, P.1    Ritson, D.J.2    Burnley, J.3    Moses, J.E.4
  • 30
    • 84868350389 scopus 로고    scopus 로고
    • A torquoselective 6π electrocyclization approach to reserpine alkaloids
    • Barcan, G. A., Patel, A., Houk, K. N. & Kwon, O. A torquoselective 6π electrocyclization approach to reserpine alkaloids. Org. Lett. 14, 5388-5391 (2012).
    • (2012) Org. Lett. , vol.14 , pp. 5388-5391
    • Barcan, G.A.1    Patel, A.2    Houk, K.N.3    Kwon, O.4
  • 32
    • 84872556766 scopus 로고    scopus 로고
    • Total synthesis of kingianin A
    • Lim, H. N. & Parker, K. A. Total synthesis of kingianin A. Org. Lett. 15, 398-401 (2013).
    • (2013) Org. Lett. , vol.15 , pp. 398-401
    • Lim, H.N.1    Parker, K.A.2
  • 34
    • 4544302358 scopus 로고    scopus 로고
    • Concise total synthesis and structure assignment of TAN-1085
    • Ohmori, K. et al. Concise total synthesis and structure assignment of TAN-1085. Angew. Chem. Int. Ed. 43, 3167-3171 (2004).
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 3167-3171
    • Ohmori, K.1
  • 37
    • 33646155347 scopus 로고    scopus 로고
    • Synthesis of indoles via 6π-electrocyclic ring closures of trienecarbamates
    • Greshock, T. J. & Funk, R. L. Synthesis of indoles via 6π-electrocyclic ring closures of trienecarbamates. J. Am. Chem. Soc. 128, 4946-4947 (2006).
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 4946-4947
    • Greshock, T.J.1    Funk, R.L.2
  • 38
    • 33745580304 scopus 로고    scopus 로고
    • An approach to the total synthesis of welwistatin
    • Greshock, T. J. & Funk, R. L. An approach to the total synthesis of welwistatin. Org. Lett. 8, 2643-2645 (2006).
    • (2006) Org. Lett. , vol.8 , pp. 2643-2645
    • Greshock, T.J.1    Funk, R.L.2
  • 39
    • 33746867893 scopus 로고    scopus 로고
    • Total syntheses of (±)-cis-trikentrin A and (±)-cis-trikentrin B via electrocyclic ring closures of 2,3-divinylpyrrolines
    • Huntley, R. J. & Funk, R. L. Total syntheses of (±)-cis-trikentrin A and (±)-cis-trikentrin B via electrocyclic ring closures of 2,3-divinylpyrrolines. Org. Lett. 8, 3403-3406 (2006).
    • (2006) Org. Lett. , vol.8 , pp. 3403-3406
    • Huntley, R.J.1    Funk, R.L.2
  • 40
    • 33750380198 scopus 로고    scopus 로고
    • A Strategy for the total synthesis of dragmacidin E. Construction of the core ring system
    • Huntley, R. J. & Funk, R. L. A Strategy for the total synthesis of dragmacidin E. Construction of the core ring system. Org. Lett. 8, 4775-4778 (2006).
    • (2006) Org. Lett. , vol.8 , pp. 4775-4778
    • Huntley, R.J.1    Funk, R.L.2
  • 41
    • 33748787678 scopus 로고    scopus 로고
    • Gold(I)-catalyzed cyclizations of silyl enol ethers: Application to the synthesis of (+)-lycopladine A
    • Staben, S. T. et al. Gold(I)-catalyzed cyclizations of silyl enol ethers: application to the synthesis of (+)-lycopladine A. Angew. Chem. Int. Ed. 45, 5991-5994 (2006).
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 5991-5994
    • Staben, S.T.1
  • 42
  • 43
    • 84918836604 scopus 로고    scopus 로고
    • Total synthesis of hapalindole-type natural products
    • Lu, Z., Yang, M., Chen, P., Xiong, X. & Li, A. Total synthesis of hapalindole-type natural products. Angew. Chem. Int. Ed. 53, 13840-13844 (2014).
    • (2014) Angew. Chem. Int. Ed. , vol.53 , pp. 13840-13844
    • Lu, Z.1    Yang, M.2    Chen, P.3    Xiong, X.4    Li, A.5
  • 44
    • 84925444061 scopus 로고    scopus 로고
    • Synthesis of indole terpenoid mimics via a functionality-tolerated Eu(fod)3-catalyzed conjugate addition
    • Xiong, X. et al. Synthesis of indole terpenoid mimics via a functionality-tolerated Eu(fod)3-catalyzed conjugate addition. Chem. Asian J. doi:10.1002/asia.201403312.
    • Chem. Asian J.
    • Xiong, X.1
  • 45
    • 84862084794 scopus 로고    scopus 로고
    • Total syntheses of anominine and tubingensin A
    • Bian, M. et al. Total syntheses of anominine and tubingensin A. J. Am. Chem. Soc. 134, 8078-8081 (2012).
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 8078-8081
    • Bian, M.1
  • 46
    • 84881117009 scopus 로고    scopus 로고
    • Total synthesis of the Daphniphyllum alkaloid daphenylline
    • Lu, Z., Li, Y., Deng, J. & Li, A. Total synthesis of the Daphniphyllum alkaloid daphenylline. Nat. Chem. 5, 679-684 (2013).
    • (2013) Nat. Chem. , vol.5 , pp. 679-684
    • Lu, Z.1    Li, Y.2    Deng, J.3    Li, A.4
  • 47
    • 84924786125 scopus 로고    scopus 로고
    • Total synthesis and antiviral activity of indolosesquiterpenoids from the xiamycin and oridamycin families
    • Meng, Z. et al. Total synthesis and antiviral activity of indolosesquiterpenoids from the xiamycin and oridamycin families. Nat. Commun. 6, 6096 (2015).
    • (2015) Nat. Commun. , vol.6 , pp. 6096
    • Meng, Z.1
  • 48
    • 84914129269 scopus 로고    scopus 로고
    • Total synthesis of rubriflordilactone A
    • Li, J., Yang, P., Yao, M., Deng, J. & Li, A. Total synthesis of rubriflordilactone A. J. Am. Chem. Soc. 136, 16477-16480 (2014).
    • (2014) J. Am. Chem. Soc. , vol.136 , pp. 16477-16480
    • Li, J.1    Yang, P.2    Yao, M.3    Deng, J.4    Li, A.5
  • 49
    • 84977245108 scopus 로고
    • Einwirkungen von aliphatischen diazoverbindungen auf thioketone
    • Staudinger, H. & Siegwart, J. Einwirkungen von aliphatischen diazoverbindungen auf thioketone. Helv. Chim. Acta 3, 833-840 (1920).
    • (1920) Helv. Chim. Acta , vol.3 , pp. 833-840
    • Staudinger, H.1    Siegwart, J.2
  • 50
    • 37049129921 scopus 로고
    • Olefin synthesis by twofold extrusion processes
    • Barton, D. H. R. & Willis, B. J. Olefin synthesis by twofold extrusion processes. J. Chem. Soc. D 1225-1226 (1970).
    • (1970) J. Chem. Soc. D , pp. 1225-1226
    • Barton, D.H.R.1    Willis, B.J.2
  • 51
    • 0002956574 scopus 로고
    • Thiocarbonyl ylides. An approach to "tetravalent sulfur" compounds
    • Kellogg, R. M. & Wassenaar, S. Thiocarbonyl ylides. An approach to "tetravalent sulfur" compounds. Tetrahedron Lett. 11, 1987-1990 (1970).
    • (1970) Tetrahedron Lett , vol.11 , pp. 1987-1990
    • Kellogg, R.M.1    Wassenaar, S.2
  • 53
    • 0026597417 scopus 로고
    • A synthesis of (+)-nonactic acid by means of the sulfur-ylide rearrangement
    • Honda, T. et al. A synthesis of (+)-nonactic acid by means of the sulfur-ylide rearrangement. Tetrahedron 48, 79-88 (1992).
    • (1992) Tetrahedron , vol.48 , pp. 79-88
    • Honda, T.1
  • 55
    • 0034852829 scopus 로고    scopus 로고
    • In control of motion: From molecular switches to molecular motors
    • Feringa, B. L. In control of motion: from molecular switches to molecular motors. Acc. Chem. Res. 34, 504-513 (2001).
    • (2001) Acc. Chem. Res. , vol.34 , pp. 504-513
    • Feringa, B.L.1
  • 56
    • 66149167198 scopus 로고    scopus 로고
    • Expeditious synthesis of contorted hexabenzocoronenes
    • Plunkett, K. N. et al. Expeditious synthesis of contorted hexabenzocoronenes. Org. Lett. 11, 2225-2228 (2009).
    • (2009) Org. Lett. , vol.11 , pp. 2225-2228
    • Plunkett, K.N.1
  • 57
    • 78650267549 scopus 로고    scopus 로고
    • Synthesis, self-assembly, and charge transporting property of contorted tetrabenzocoronenes
    • Zhang, X. et al. Synthesis, self-assembly, and charge transporting property of contorted tetrabenzocoronenes. J. Org. Chem. 75, 8069-8077 (2010).
    • (2010) J. Org. Chem. , vol.75 , pp. 8069-8077
    • Zhang, X.1
  • 58
    • 0031871450 scopus 로고    scopus 로고
    • Rapid conversion of phenols to p-benzoquinones under acidic conditions with lead dioxide
    • Omura, K. Rapid conversion of phenols to p-benzoquinones under acidic conditions with lead dioxide. Synthesis (Mass). 1145-1148 (1998).
    • (1998) Synthesis (Mass) , pp. 1145-1148
    • Omura, K.1
  • 59
    • 0003002473 scopus 로고
    • γ-Sulphenylation of αβ-unsaturated aldehydes, ketones, and esters: The use of O-silylated dienolates
    • Fleming, I., Goldhill, J. & Paterson, I. γ-Sulphenylation of αβ-unsaturated aldehydes, ketones, and esters: the use of O-silylated dienolates. Tetrahedron Lett. 20, 3205-3208 (1979).
    • (1979) Tetrahedron Lett , vol.20 , pp. 3205-3208
    • Fleming, I.1    Goldhill, J.2    Paterson, I.3
  • 60
    • 49249152005 scopus 로고
    • Regiospecific syntheses of quinones using vinylketene acetals derived from unsaturated esters
    • Savard, J. & Brassard, P. Regiospecific syntheses of quinones using vinylketene acetals derived from unsaturated esters. Tetrahedron Lett. 20, 4911-4914 (1979).
    • (1979) Tetrahedron Lett , vol.20 , pp. 4911-4914
    • Savard, J.1    Brassard, P.2
  • 61
    • 7144259775 scopus 로고    scopus 로고
    • A convergent total synthesis of the michellamines
    • Bringmann, G. et al. A convergent total synthesis of the michellamines. J. Org. Chem. 63, 1090-1097 (1998).
    • (1998) J. Org. Chem. , vol.63 , pp. 1090-1097
    • Bringmann, G.1
  • 62
    • 0000295971 scopus 로고    scopus 로고
    • Syntheses of anthracenones. 2. Preparation of 1,8-dimethoxy-(dimethylanthralin) and 4,5-dihydroxy-9(10H)-anthracenone (isoanthralin): A revision
    • Prinz, H., Burgemeister, T., Wiegrebe, W. & Müller, K. Syntheses of anthracenones. 2. Preparation of 1,8-dimethoxy-(dimethylanthralin) and 4,5-dihydroxy-9(10H)-anthracenone (isoanthralin): a revision. J. Org. Chem. 61, 2857-2860 (1996).
    • (1996) J. Org. Chem. , vol.61 , pp. 2857-2860
    • Prinz, H.1    Burgemeister, T.2    Wiegrebe, W.3    Müller, K.4
  • 64
    • 33845223512 scopus 로고
    • Synthesis of polyfluoroaromatic magnesium compounds through the exchange reaction
    • Tamborski, C. & Moore, G. J. Synthesis of polyfluoroaromatic magnesium compounds through the exchange reaction. J. Organomet. Chem. 26, 153-156 (1971).
    • (1971) J. Organomet. Chem. , vol.26 , pp. 153-156
    • Tamborski, C.1    Moore, G.J.2
  • 65
    • 0000937249 scopus 로고
    • Preparation of pyridyl Grignard reagents and cross coupling reactions with sulfoxides bearing azaheterocycles
    • Furukawa, N., Shibutani, T. & Fujihara, H. Preparation of pyridyl Grignard reagents and cross coupling reactions with sulfoxides bearing azaheterocycles. Tetrahedron Lett. 28, 5845-5848 (1987).
    • (1987) Tetrahedron Lett , vol.28 , pp. 5845-5848
    • Furukawa, N.1    Shibutani, T.2    Fujihara, H.3
  • 66
    • 0141645562 scopus 로고    scopus 로고
    • Highly functionalized organomagnesium reagents prepared through halogen-metal exchange
    • Knochel, P. et al. Highly functionalized organomagnesium reagents prepared through halogen-metal exchange. Angew. Chem. Int. Ed. 42, 4302 (2003).
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 4302
    • Knochel, P.1
  • 67
    • 0002856892 scopus 로고
    • Condensation of a chiral tetrahydro-2-furanthione with diazocarbonyl compounds
    • Takano, S., Tomita, S., Takahashi, M. & Ogasawara, K. Condensation of a chiral tetrahydro-2-furanthione with diazocarbonyl compounds. Synthesis (Mass). 1116-1117 (1987).
    • (1987) Synthesis (Mass) , pp. 1116-1117
    • Takano, S.1    Tomita, S.2    Takahashi, M.3    Ogasawara, K.4
  • 68
    • 84954241151 scopus 로고
    • Generaton of thiocarbonyl ylides from the rhodium(II)-catalyzed cyclization of diazothiocarbonyl compounds
    • Padwa, A., Kinder, F. R. & Zhi, L. Generaton of thiocarbonyl ylides from the rhodium(II)-catalyzed cyclization of diazothiocarbonyl compounds. Synlett 287-288 (1991).
    • (1991) Synlett , pp. 287-288
    • Padwa, A.1    Kinder, F.R.2    Zhi, L.3
  • 69
    • 0000984982 scopus 로고
    • Glyconothio-O-lactones part II. Cycloaddition to dienes, diazomethane, and carbenoids
    • Hürzeler, M., Bernet, B., Mäder, T. & Vasella, A. Glyconothio-O-lactones part II. cycloaddition to dienes, diazomethane, and carbenoids. Helv. Chim. Acta 76, 1779-1801 (1993).
    • (1993) Helv. Chim. Acta , vol.76 , pp. 1779-1801
    • Hürzeler, M.1    Bernet, B.2    Mäder, T.3    Vasella, A.4
  • 70
    • 0029988230 scopus 로고    scopus 로고
    • Carbenoid reactions of dimethyl diazomalonate with aromatic thioketones and 1,3-thiazole-5(4H)-thiones
    • Mlostón, G. & Heimgartner, H. Carbenoid reactions of dimethyl diazomalonate with aromatic thioketones and 1,3-thiazole-5(4H)-thiones. Helv. Chim. Acta 79, 1785-1792 (1996).
    • (1996) Helv. Chim. Acta , vol.79 , pp. 1785-1792
    • Mlostón, G.1    Heimgartner, H.2


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