메뉴 건너뛰기




Volumn 5, Issue , 2014, Pages

Benzene construction via organocatalytic formal [3+3] cycloaddition reaction

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; ALKENE DERIVATIVE; ALKYL GROUP; BENZENE; CARBENE; CARBONYL DERIVATIVE; NUCLEOPHILE; ORGANIC SOLVENT; TETRAHYDROFURAN; TRANSITION ELEMENT;

EID: 84923253531     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms6027     Document Type: Article
Times cited : (95)

References (57)
  • 1
    • 22244470396 scopus 로고    scopus 로고
    • Structure determination of salvadorin, a novel dimeric dihydroisocoumarin from salvadora oleoides, by NMR spectroscopy
    • Mahmood, T., Ahmed, E. & Malik, A. Structure determination of salvadorin, a novel dimeric dihydroisocoumarin from salvadora oleoides, by NMR spectroscopy. Magn. Reson. Chem. 43, 670-672 (2005).
    • (2005) Magn. Reson. Chem. , vol.43 , pp. 670-672
    • Mahmood, T.1    Ahmed, E.2    Malik, A.3
  • 2
    • 0022512448 scopus 로고
    • 3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. 5. 6-(Fluoren-9-yl)-and 6(Fluoren-9-ylidenyl)-3, 5-dihydroxyhexanoic acids and their lactone derivatives
    • Stokker, G. E., Alberts, A. W., Gilfillan, J. L., Huff, J. W. & Smith, R. L. 3-hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. 5. 6-(Fluoren-9-yl)-and 6(Fluoren-9-ylidenyl)-3, 5-dihydroxyhexanoic acids and their lactone derivatives. J. Med. Chem. 29, 852-855 (1986).
    • (1986) J. Med. Chem. , vol.29 , pp. 852-855
    • Stokker, G.E.1    Alberts, A.W.2    Gilfillan, J.L.3    Huff, J.W.4    Smith, R.L.5
  • 3
    • 84884285185 scopus 로고    scopus 로고
    • 3-Ylidenephthalides as a new class of transient receptor potential channel TRPA1 and TRPM8 modulators
    • Ortar, G. et al. 3-ylidenephthalides as a new class of transient receptor potential channel TRPA1 and TRPM8 modulators. Bioorg. Med. Chem. Lett. 23, 5614-5618 (2013).
    • (2013) Bioorg. Med. Chem. Lett. , vol.23 , pp. 5614-5618
    • Ortar, G.1
  • 4
    • 84885478893 scopus 로고
    • 2,4,6-Tribromobenzoic acid
    • Robison, M. M. & Robison, B. L. 2,4,6-tribromobenzoic acid. Org. Synth. 36, 94-97 (1956).
    • (1956) Org. Synth. , vol.36 , pp. 94-97
    • Robison, M.M.1    Robison, B.L.2
  • 7
    • 84868355670 scopus 로고    scopus 로고
    • Ruthenium (II)-catalyzed C-H bond activation and functionalization
    • Arockiam, P. B., Bruneau, C. & Dixneuf, P. H. Ruthenium (II)-catalyzed C-H bond activation and functionalization. Chem. Rev. 112, 5879-5918 (2012).
    • (2012) Chem. Rev. , vol.112 , pp. 5879-5918
    • Arockiam, P.B.1    Bruneau, C.2    Dixneuf, P.H.3
  • 8
    • 84863446276 scopus 로고    scopus 로고
    • Weak coordination as a powerful means for developing broadly useful C-H functionalization reactions
    • Engle, K. M., Mei, T.-S., Wasa, M. & Yu, J.-Q. Weak coordination as a powerful means for developing broadly useful C-H functionalization reactions. Acc. Chem. Res. 45, 788-802 (2012).
    • (2012) Acc. Chem. Res. , vol.45 , pp. 788-802
    • Engle, K.M.1    Mei, T.-S.2    Wasa, M.3    Yu, J.-Q.4
  • 10
    • 79957713071 scopus 로고    scopus 로고
    • Recent advances in [2 + 2 + 2] cycloaddtion reactions
    • Domínguez, G. & Pérez-Castells, J. Recent advances in [2 + 2 + 2] cycloaddtion reactions. Chem. Soc. Rev. 40, 3430-3444 (2011).
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 3430-3444
    • Domínguez, G.1    Pérez-Castells, J.2
  • 12
    • 4143051292 scopus 로고    scopus 로고
    • Nucleophilic carbenes in asymmetric organocatalysis
    • Enders, D. & Balensiefer, T. Nucleophilic carbenes in asymmetric organocatalysis. Acc. Chem. Res. 37, 534-541 (2004).
    • (2004) Acc. Chem. Res. , vol.37 , pp. 534-541
    • Enders, D.1    Balensiefer, T.2
  • 13
    • 28244479394 scopus 로고    scopus 로고
    • Extending mechanistic routes in heterazolium catalysis-promising concepts for versatile synthetic methods
    • Zeitler, K. Extending mechanistic routes in heterazolium catalysis-promising concepts for versatile synthetic methods. Angew. Chem. Int. Ed. 44, 7506-7510 (2005).
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 7506-7510
    • Zeitler, K.1
  • 15
    • 56549104231 scopus 로고    scopus 로고
    • Recent advances in carbon-carbon bond-forming reactions involving homoenolates generated by NHC catalysis
    • Nair, V., Vellalath, S. & Babu, B. P. Recent advances in carbon-carbon bond-forming reactions involving homoenolates generated by NHC catalysis. Chem. Soc. Rev. 37, 2691-2698 (2008).
    • (2008) Chem. Soc. Rev. , vol.37 , pp. 2691-2698
    • Nair, V.1    Vellalath, S.2    Babu, B.P.3
  • 16
    • 79958213157 scopus 로고    scopus 로고
    • Asymmetric N-heterocyclic Carbene (NHC) catalyzed acyl anion reactions
    • Vora, H. U. & Rovis, T. Asymmetric N-heterocyclic Carbene (NHC) catalyzed acyl anion reactions. Aldrichim. Acta 44, 3-11 (2011).
    • (2011) Aldrichim. Acta , vol.44 , pp. 3-11
    • Vora, H.U.1    Rovis, T.2
  • 17
    • 84864286666 scopus 로고    scopus 로고
    • NHCs in asymmetric organocatalysis: Recent advances in azolium enolate generation and reactivity
    • Douglas, J., Churchill, G. & Smith, A. D. NHCs in asymmetric organocatalysis: recent advances in azolium enolate generation and reactivity. Synthesis. (Mass). 44, 2295-2309 (2012).
    • (2012) Synthesis. (Mass) , vol.44 , pp. 2295-2309
    • Douglas, J.1    Churchill, G.2    Smith, A.D.3
  • 18
    • 77950278547 scopus 로고    scopus 로고
    • Discovering new reactions with N-heterocyclic carbene catalysis
    • Phillips, E. M., Chan, A. & Scheidt, K. A. Discovering new reactions with N-heterocyclic carbene catalysis. Aldrichim. Acta 42, 55-66 (2009).
    • (2009) Aldrichim. Acta , vol.42 , pp. 55-66
    • Phillips, E.M.1    Chan, A.2    Scheidt, K.A.3
  • 19
    • 84869460648 scopus 로고    scopus 로고
    • A continuum of progress: Applications of N-hetereocyclic carbene catalysis in total synthesis
    • Izquierdo, J., Hutson, G. E., Cohen, D. T. & Scheidt, K. A. A continuum of progress: applications of N-hetereocyclic carbene catalysis in total synthesis. Angew. Chem. Int. Ed. 51, 11686-11698 (2012).
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 11686-11698
    • Izquierdo, J.1    Hutson, G.E.2    Cohen, D.T.3    Scheidt, K.A.4
  • 20
    • 84875799416 scopus 로고    scopus 로고
    • Acyl anion free N-heterocyclic carbene organocatalysis
    • Ryan, S. J., Candish, L. & Lupton, D. W. Acyl anion free N-heterocyclic carbene organocatalysis. Chem. Soc. Rev. 42, 4906-4917 (2013).
    • (2013) Chem. Soc. Rev. , vol.42 , pp. 4906-4917
    • Ryan, S.J.1    Candish, L.2    Lupton, D.W.3
  • 21
    • 79957777084 scopus 로고    scopus 로고
    • N-mesityl substituted chiral triazolium salts: Opening a new world of N-heterocyclic carbene catalysis
    • Chiang, P.-C. & Bode, J. W. N-mesityl substituted chiral triazolium salts: opening a new world of N-heterocyclic carbene catalysis. TCI Mail 149, 2-17 (2011).
    • (2011) TCI Mail , vol.149 , pp. 2-17
    • Chiang, P.-C.1    Bode, J.W.2
  • 22
    • 84884881290 scopus 로고    scopus 로고
    • Carbene catalysis: An internal affair
    • Bode, J. W. Carbene catalysis: an internal affair. Nat. Chem. 5, 813-815 (2013).
    • (2013) Nat. Chem. , vol.5 , pp. 813-815
    • Bode, J.W.1
  • 23
    • 84859747983 scopus 로고    scopus 로고
    • Organocatalytic umpolung: N-heterocyclic carbenes and beyond
    • Bugaut, X. & Glorius, F. Organocatalytic umpolung: N-heterocyclic carbenes and beyond. Chem. Soc. Rev. 41, 3511-3522 (2012).
    • (2012) Chem. Soc. Rev. , vol.41 , pp. 3511-3522
    • Bugaut, X.1    Glorius, F.2
  • 25
    • 0025370313 scopus 로고
    • A new and versatile route for the synthesis of highly substituted benzenoids
    • Robl, J. A. A new and versatile route for the synthesis of highly substituted benzenoids. Tetrahedron Lett. 31, 3421-3424 (1990).
    • (1990) Tetrahedron Lett. , vol.31 , pp. 3421-3424
    • Robl, J.A.1
  • 26
    • 0002505045 scopus 로고    scopus 로고
    • Benzoin-type condensations of formaldehyde catalyzed by stable carbenes
    • Teles, J. H. et al. Benzoin-type condensations of formaldehyde catalyzed by stable carbenes. Helv. Chim. Acta 79, 61-83 (1996).
    • (1996) Helv. Chim. Acta , vol.79 , pp. 61-83
    • Teles, J.H.1
  • 27
    • 0342953575 scopus 로고    scopus 로고
    • Synthesis and reactivities of 1,3-dimentyl-2-(α-hydroxybenzyl) imidazolium and 1,3-dimentyl-2-(α-hydroxybenzyl) benzimidazolium iodides
    • Miyashita, A. et al. Synthesis and reactivities of 1,3-dimentyl-2-(α-hydroxybenzyl) imidazolium and 1,3-dimentyl-2-(α-hydroxybenzyl) benzimidazolium iodides. Heterocyles 44, 417-426 (1997).
    • (1997) Heterocyles , vol.44 , pp. 417-426
    • Miyashita, A.1
  • 28
    • 84874593137 scopus 로고    scopus 로고
    • Mechanistic insights into the trazolylidene-catalysed Stetter and benzoin reactions: Role of the N-aryl substituent
    • Collett, C. J. et al. Mechanistic insights into the trazolylidene-catalysed Stetter and benzoin reactions: role of the N-aryl substituent. Chem. Sci. 4, 1514-1522 (2013).
    • (2013) Chem. Sci. , vol.4 , pp. 1514-1522
    • Collett, C.J.1
  • 29
    • 78649563244 scopus 로고    scopus 로고
    • NHC-catalyzed michael addition to α,β-unsaturated aldehydes by redox activation
    • Sarkar, S. D. & Studer, A. NHC-catalyzed michael addition to α,β-unsaturated aldehydes by redox activation. Angew. Chem. Int. Ed. 49, 9266-9269 (2010).
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 9266-9269
    • Sarkar, S.D.1    Studer, A.2
  • 30
    • 79961050463 scopus 로고    scopus 로고
    • Enantioselective N-heterocyclic carbene-catalyzed michael addition to α,β-unsaturated aldehydes by redox oxidation
    • Rong, Z.-Q., Jia, M.-Q. & You, S.-L. Enantioselective N-heterocyclic carbene-catalyzed michael addition to α,β-unsaturated aldehydes by redox oxidation. Org. Lett. 13, 4080-4083 (2011).
    • (2011) Org. Lett. , vol.13 , pp. 4080-4083
    • Rong, Z.-Q.1    Jia, M.-Q.2    You, S.-L.3
  • 31
    • 84870485888 scopus 로고    scopus 로고
    • N-heterocyclic-carbene-catalyzed asymmetric oxidative hetero-Diels- Alder reactions with simple aliphatic aldehydes
    • Zhao, X., Ruhl, K. E. & Rovis, T. N-heterocyclic-carbene-catalyzed asymmetric oxidative hetero-Diels- Alder reactions with simple aliphatic aldehydes. Angew. Chem. Int. Ed. 51, 12330-12333 (2012).
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 12330-12333
    • Zhao, X.1    Ruhl, K.E.2    Rovis, T.3
  • 32
    • 84865856031 scopus 로고    scopus 로고
    • Enantioselective, NHC-catalyzed annulations of trisubstituted enals and cyclic N-sulfonylimines via α,β-unsaturated acyl azoliums
    • Kravina, A. G., Mahatthananchai, J. & Bode, J. W. Enantioselective, NHC-catalyzed annulations of trisubstituted enals and cyclic N-sulfonylimines via α,β-unsaturated acyl azoliums. Angew. Chem. Int. Ed. 51, 9433-9436 (2012).
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 9433-9436
    • Kravina, A.G.1    Mahatthananchai, J.2    Bode, J.W.3
  • 33
    • 84861633806 scopus 로고    scopus 로고
    • Oxidative γ-addition of enals to trifuoromethyl ketones: Enantioselectivity control via Lewis acid/N-heterocyclic carbene cooperative catalysis
    • Mo, J., Chen, X. & Chi, Y. R. Oxidative γ-addition of enals to trifuoromethyl ketones: enantioselectivity control via Lewis acid/N-heterocyclic carbene cooperative catalysis. J. Am. Chem. Soc. 134, 8810-8813 (2012).
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 8810-8813
    • Mo, J.1    Chen, X.2    Chi, Y.R.3
  • 34
    • 80052008516 scopus 로고    scopus 로고
    • N-heterocyclic carbene-catalyzed cyclization of unsaturated acyl chlorides and ketones
    • Shen, L.-T., Shao, P.-L. & Ye, S. N-heterocyclic carbene-catalyzed cyclization of unsaturated acyl chlorides and ketones. Adv. Synth. Catal. 353, 1943-1948 (2011).
    • (2011) Adv. Synth. Catal. , vol.353 , pp. 1943-1948
    • Shen, L.-T.1    Shao, P.-L.2    Ye, S.3
  • 35
    • 84885096747 scopus 로고    scopus 로고
    • Organocatalytic enantioselective γ-aminoalkylation of unsaturated ester: Access to pipecolic acid derivatives
    • Xu, J., Jin, Z. & Chi, Y. R. Organocatalytic enantioselective γ-aminoalkylation of unsaturated ester: access to pipecolic acid derivatives. Org. Lett. 15, 5028-5031 (2013).
    • (2013) Org. Lett. , vol.15 , pp. 5028-5031
    • Xu, J.1    Jin, Z.2    Chi, Y.R.3
  • 36
    • 33745940097 scopus 로고    scopus 로고
    • N-heterocyclic carbene-catalyzed reaction of chalcones and enals via homoenolate: An efficient synthesis of 1,4,5-Trisubstituted cyclopentenes
    • Nair, V., Vellalath, S., Poonoth, M. & Suresh, E. N-heterocyclic carbene-catalyzed reaction of chalcones and enals via homoenolate: an efficient synthesis of 1,4,5-Trisubstituted cyclopentenes. J. Am. Chem. Soc. 128, 8736-8737 (2006).
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 8736-8737
    • Nair, V.1    Vellalath, S.2    Poonoth, M.3    Suresh, E.4
  • 37
    • 67650551310 scopus 로고    scopus 로고
    • α′-hydroxyenones as mechanistic probes and scope-expanding surrogates for α,β-Unsaturated aldehydes in N-heterocyclic carbene- catalyzed reactions
    • Chiang, P.-C., Rommel, M. & Bode, J. W. α′-hydroxyenones as mechanistic probes and scope-expanding surrogates for α,β-Unsaturated aldehydes in N-heterocyclic carbene- catalyzed reactions. J. Am. Chem. Soc. 131, 8714-8718 (2009).
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 8714-8718
    • Chiang, P.-C.1    Rommel, M.2    Bode, J.W.3
  • 38
    • 77951079080 scopus 로고    scopus 로고
    • Cooperative N-heterocyclic carbene/Lewis acid catalysis for highly stereoselective annulation reactions with homoenolates
    • Cardinal-David, B., Raup, D. E. A. & Scheidt, K. A. Cooperative N-heterocyclic carbene/Lewis acid catalysis for highly stereoselective annulation reactions with homoenolates. J. Am. Chem. Soc. 132, 5345-5347 (2010).
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 5345-5347
    • Cardinal-David, B.1    Raup, D.E.A.2    Scheidt, K.A.3
  • 39
    • 79953853387 scopus 로고    scopus 로고
    • N-heterocyclic carbene-catalyzed (4 + 2) cycloaddtion/ decarboxylation of silyl dienol ethers with α,β-unsaturated acid fluorides
    • Ryan, S. J., Candish, L. & Lupton, D. W. N-heterocyclic carbene-catalyzed (4 + 2) cycloaddtion/ decarboxylation of silyl dienol ethers with α,β-unsaturated acid fluorides. J. Am. Chem. Soc. 133, 4694-4697 (2011).
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 4694-4697
    • Ryan, S.J.1    Candish, L.2    Lupton, D.W.3
  • 40
    • 79960078229 scopus 로고    scopus 로고
    • Palladium-catalyzed aerobic dehydrogeneation of substituted cyclohexanones to phenols
    • Izawa, Y., Pun, D. & Stahl, S. S. Palladium-catalyzed aerobic dehydrogeneation of substituted cyclohexanones to phenols. Science 333, 209-213 (2011).
    • (2011) Science , vol.333 , pp. 209-213
    • Izawa, Y.1    Pun, D.2    Stahl, S.S.3
  • 41
    • 84868350371 scopus 로고    scopus 로고
    • Pd-catalyzed synthesis of aryl amines via oxidative aromatization of cyclic ketones and amines with molecular oxygen
    • Girard, S. A. et al. Pd-catalyzed synthesis of aryl amines via oxidative aromatization of cyclic ketones and amines with molecular oxygen. Org. Lett. 14, 5606-5609 (2012).
    • (2012) Org. Lett. , vol.14 , pp. 5606-5609
    • Girard, S.A.1
  • 42
    • 68949096781 scopus 로고    scopus 로고
    • Metathesis in the synthesis of aromatic compounds
    • van Otterlo, W. A. & de Koning, C. B. Metathesis in the synthesis of aromatic compounds. Chem. Rev. 109, 3743-3782 (2009).
    • (2009) Chem. Rev. , vol.109 , pp. 3743-3782
    • Van Otterlo, W.A.1    De Koning, C.B.2
  • 43
    • 24044495219 scopus 로고    scopus 로고
    • One-step assembly of functionalized γ-butyrolactones from benzoins or benzaldehydes via an N-heterocyclic carbene-mediated tandem reaction
    • Ye, W., Cai, G., Zhuang, Z., Jia, X. & Zhai, H. One-step assembly of functionalized γ-butyrolactones from benzoins or benzaldehydes via an N-heterocyclic carbene-mediated tandem reaction. Org. Lett. 7, 3769-3771 (2005).
    • (2005) Org. Lett. , vol.7 , pp. 3769-3771
    • Ye, W.1    Cai, G.2    Zhuang, Z.3    Jia, X.4    Zhai, H.5
  • 44
    • 10044249952 scopus 로고    scopus 로고
    • Organocatalyzed conjugate umpolung of α,β-Unsaturated aldehydes for the synthesis of γ-butyrolactones
    • Burstein, C. & Glorius, F. Organocatalyzed conjugate umpolung of α,β-Unsaturated aldehydes for the synthesis of γ-butyrolactones. Angew. Chem. Int. Ed. 43, 6205-6208 (2004).
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 6205-6208
    • Burstein, C.1    Glorius, F.2
  • 45
    • 3543074145 scopus 로고    scopus 로고
    • Conversion of α-haloaldehydes into acylating agents by and internal redox reaction catalyzed by nucleophilic carbenes
    • Reynolds, N. T., de Alaniz, J. R. & Rovis, T. Conversion of α-haloaldehydes into acylating agents by and internal redox reaction catalyzed by nucleophilic carbenes. J. Am. Chem. Soc. 126, 9518-9519 (2004).
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 9518-9519
    • Reynolds, N.T.1    De Alaniz, J.R.2    Rovis, T.3
  • 46
    • 36148946729 scopus 로고    scopus 로고
    • N-heterocyclic carbene-catalyzed redox amidations of α-functionalized aldehydes with amines
    • Bode, J. W. & Sohn, S. S. N-heterocyclic carbene-catalyzed redox amidations of α-functionalized aldehydes with amines. J. Am. Chem. Soc. 129, 13798-13799 (2007).
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 13798-13799
    • Bode, J.W.1    Sohn, S.S.2
  • 47
    • 0037667546 scopus 로고
    • Acyloin condensation by thiazolium ion catalysis: Butyroin
    • Stetter, H. & Kulmann, H. Acyloin condensation by thiazolium ion catalysis: butyroin. Org. Synth. 62, 170-174 (1984).
    • (1984) Org. Synth. , vol.62 , pp. 170-174
    • Stetter, H.1    Kulmann, H.2
  • 48
    • 33846644953 scopus 로고
    • Nitrobenzene aldehyde oxidations catalyzed by the conjugate bases of thiazolium ions
    • Castells, J., Llitjos, H. & Moreno-Manas, M. Nitrobenzene aldehyde oxidations catalyzed by the conjugate bases of thiazolium ions. Tetrahedron Lett. 2, 205-206 (1977).
    • (1977) Tetrahedron Lett. , vol.2 , pp. 205-206
    • Castells, J.1    Llitjos, H.2    Moreno-Manas, M.3
  • 49
    • 33747192855 scopus 로고    scopus 로고
    • Synthesis of fluorenones based on a '[3 + 3] cyclization/Suzuki cross-coupling/Friedel-Crafts acylation' strategy
    • Reim, S., Lau, M. & Langer, P. Synthesis of fluorenones based on a '[3 + 3] cyclization/Suzuki cross-coupling/Friedel-Crafts acylation' strategy. Tetrahedron Lett. 47, 6903-6905 (2006).
    • (2006) Tetrahedron Lett. , vol.47 , pp. 6903-6905
    • Reim, S.1    Lau, M.2    Langer, P.3
  • 50
    • 83055177179 scopus 로고    scopus 로고
    • Trifluoromethylation of arenes and heteroarenes by means of photoredox catalysis
    • Nagib, D. A. & Macmillan, D. W. C. Trifluoromethylation of arenes and heteroarenes by means of photoredox catalysis. Nature 480, 224-228 (2011).
    • (2011) Nature , vol.480 , pp. 224-228
    • Nagib, D.A.1    Macmillan, D.W.C.2
  • 51
    • 84870541226 scopus 로고    scopus 로고
    • Practical and innate carbon-hydrogen functionalization of heterocycles
    • Fujiwara, Y. et al. Practical and innate carbon-hydrogen functionalization of heterocycles. Nature 492, 96-99 (2012).
    • (2012) Nature , vol.492 , pp. 96-99
    • Fujiwara, Y.1
  • 52
    • 84887566303 scopus 로고    scopus 로고
    • Profound methyl effects in drug discovery and a call for new C-H methylation reactions
    • Schönherr, H. & Cernak, T. Profound methyl effects in drug discovery and a call for new C-H methylation reactions. Angew. Chem. Int. Ed. 52, 12256-12267 (2013).
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 12256-12267
    • Schönherr, H.1    Cernak, T.2
  • 53
    • 33947644069 scopus 로고    scopus 로고
    • 3C-H bonds in simple carboxylid acids
    • 3C-H bonds in simple carboxylid acids. J. Am. Chem. Soc. 129, 3510-3511 (2007).
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 3510-3511
    • Giri, R.1
  • 54
    • 84880146997 scopus 로고    scopus 로고
    • C-H functionalization logic enables synthesis of (+)-Hongoquercin A and related compounds
    • Rosen, B. R. et al. C-H functionalization logic enables synthesis of (+)-Hongoquercin A and related compounds. Angew. Chem. Int. Ed. 52, 7317-7320 (2013).
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 7317-7320
    • Rosen, B.R.1
  • 55
    • 20244377229 scopus 로고    scopus 로고
    • 2-like Dopamine receptor agonists
    • 2-like Dopamine receptor agonists. J. Med. Chem. 48, 2646-2654 (2005).
    • (2005) J. Med. Chem. , vol.48 , pp. 2646-2654
    • Antonio, D.S.1
  • 56
    • 0033566092 scopus 로고    scopus 로고
    • 2,7-Disubstituted amdofluorenone derivatives as inhibitors of human telomerase
    • Perry, P. J. et al. 2,7-Disubstituted amdofluorenone derivatives as inhibitors of human telomerase. J. Med. Chem. 42, 2679-2684 (1999).
    • (1999) J. Med. Chem. , vol.42 , pp. 2679-2684
    • Perry, P.J.1
  • 57
    • 72249117763 scopus 로고    scopus 로고
    • Nonpeptide Urotesin-II receptor antagonist: A new ligand class based on piperazino-phthalimide and piperazino-isoindolinone subunits
    • Lawson, E. C. et al. Nonpeptide Urotesin-II receptor antagonist: a new ligand class based on piperazino-phthalimide and piperazino-isoindolinone subunits. J. Med. Chem. 52, 7432-7445 (2009).
    • (2009) J. Med. Chem. , vol.52 , pp. 7432-7445
    • Lawson, E.C.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.