메뉴 건너뛰기




Volumn , Issue , 2014, Pages 67-98

DNA-Compatible Chemistry

Author keywords

DNA compatible chemistries; DNA encoded libraries (DELs)

Indexed keywords

LIBRARIES;

EID: 84939823003     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/9781118832738.ch4     Document Type: Chapter
Times cited : (16)

References (70)
  • 1
    • 32344453283 scopus 로고    scopus 로고
    • DNA-templated synthesis in organic solvents
    • Rozenman, M. M., Liu, D. R. (2006). DNA-templated synthesis in organic solvents. ChemBioChem 7, 253-256.
    • (2006) ChemBioChem , vol.7 , pp. 253-256
    • Rozenman, M.M.1    Liu, D.R.2
  • 2
    • 4544357020 scopus 로고    scopus 로고
    • DNA-templated organic synthesis: nature's strategy for controlling chemical reactivity applied to synthetic molecules
    • Li, X., Liu, D. R. (2004). DNA-templated organic synthesis: nature's strategy for controlling chemical reactivity applied to synthetic molecules. Angew. Chem. Int. Ed. 43, 4848-4870.
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 4848-4870
    • Li, X.1    Liu, D.R.2
  • 3
    • 79959878459 scopus 로고    scopus 로고
    • A sequential strand-displacement strategy enables efficient six-step DNA-templated synthesis
    • He, Y., Liu, D. R. (2011). A sequential strand-displacement strategy enables efficient six-step DNA-templated synthesis. J. Am. Chem. Soc. 133, 9972-9975.
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 9972-9975
    • He, Y.1    Liu, D.R.2
  • 5
    • 0036263805 scopus 로고    scopus 로고
    • Expanding the reaction scope of DNA-templated synthesis
    • Gartner, Z. J., Kanan, M. W., Liu, D. R. (2002). Expanding the reaction scope of DNA-templated synthesis. Angew. Chem. Int. Ed. 41, 1796-1800.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 1796-1800
    • Gartner, Z.J.1    Kanan, M.W.2    Liu, D.R.3
  • 10
    • 4644350506 scopus 로고    scopus 로고
    • DNA-templated organic synthesis and selection of a library of macrocycles
    • Gartner, Z. J., Tse, B. N., Grubina, R., Doyon, J. B., Snyder, T. M., Liu, D. R. (2004). DNA-templated organic synthesis and selection of a library of macrocycles. Science 305, 1601-1605.
    • (2004) Science , vol.305 , pp. 1601-1605
    • Gartner, Z.J.1    Tse, B.N.2    Grubina, R.3    Doyon, J.B.4    Snyder, T.M.5    Liu, D.R.6
  • 11
    • 79251640637 scopus 로고    scopus 로고
    • A biomolecule-compatible visiblelight- induced azide reduction from a DNA-encoded reaction-discovery system
    • Chen, Y., Kamlet, A. S., Steinman, J. B., Liu, D. R. (2011). A biomolecule-compatible visiblelight- induced azide reduction from a DNA-encoded reaction-discovery system. Nat. Chem. 3, 146-153.
    • (2011) Nat. Chem. , vol.3 , pp. 146-153
    • Chen, Y.1    Kamlet, A.S.2    Steinman, J.B.3    Liu, D.R.4
  • 14
    • 36849070953 scopus 로고    scopus 로고
    • Development and initial application of a hybridization-independent, DNA-encoded reaction discovery system compatible with organic solvents
    • Rozenman, M. M., Kanan, M. W., Liu, D. R. (2007). Development and initial application of a hybridization-independent, DNA-encoded reaction discovery system compatible with organic solvents. J. Am. Chem. Soc. 129, 14933-14938.
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 14933-14938
    • Rozenman, M.M.1    Kanan, M.W.2    Liu, D.R.3
  • 15
    • 55249121613 scopus 로고    scopus 로고
    • Design and synthesis of a novel DNA-encoded chemical library using Diels-Alder cycloadditions
    • Buller, F., Mannocci, L., Zhang, Y., Dumelin, C. E., Scheuermann, J., Neri, D. (2008). Design and synthesis of a novel DNA-encoded chemical library using Diels-Alder cycloadditions. Bioorg. Med. Chem. Lett. 18, 5926-5931.
    • (2008) Bioorg. Med. Chem. Lett. , vol.18 , pp. 5926-5931
    • Buller, F.1    Mannocci, L.2    Zhang, Y.3    Dumelin, C.E.4    Scheuermann, J.5    Neri, D.6
  • 17
    • 84860132285 scopus 로고    scopus 로고
    • Consecutive signal amplification for DNA detection based on de novo fluorophore synthesis and host-guest chemistry
    • Chen, X. -H., Roloff, A., Seitz, O. (2012). Consecutive signal amplification for DNA detection based on de novo fluorophore synthesis and host-guest chemistry. Angew. Chem. Int. Ed. 51, 4479-4483.
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 4479-4483
    • Chen, X.-H.1    Roloff, A.2    Seitz, O.3
  • 18
    • 0034829726 scopus 로고    scopus 로고
    • The generality of DNA-templated synthesis as a basis for evolving non-natural small molecules
    • Gartner, Z. J., Liu, D. R. (2001). The generality of DNA-templated synthesis as a basis for evolving non-natural small molecules. J. Am. Chem. Soc. 123, 6961-6963.
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 6961-6963
    • Gartner, Z.J.1    Liu, D.R.2
  • 19
    • 1942456806 scopus 로고    scopus 로고
    • Translation of DNA into synthetic N-acyloxazolidines
    • Li, X., Gartner, Z. J., Tse, B. N., Liu, D. R. (2004). Translation of DNA into synthetic N-acyloxazolidines. J. Am. Chem. Soc. 126, 5090-5092.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 5090-5092
    • Li, X.1    Gartner, Z.J.2    Tse, B.N.3    Liu, D.R.4
  • 20
    • 4944255180 scopus 로고    scopus 로고
    • Reaction discovery enabled by DNA-templated synthesis and in vitro selection
    • Kanan, M. W., Rozenman, M. M., Sakurai, K., Snyder, T. M., Liu, D. R., (2004). Reaction discovery enabled by DNA-templated synthesis and in vitro selection. Nature 431, 545-549.
    • (2004) Nature , vol.431 , pp. 545-549
    • Kanan, M.W.1    Rozenman, M.M.2    Sakurai, K.3    Snyder, T.M.4    Liu, D.R.5
  • 22
    • 0000234211 scopus 로고
    • Transamidation reactions using β-lactams. The synthesis of homaline
    • Wasserman, H. H., Berger, G. D., Cho, K. R. (1982). Transamidation reactions using β-lactams. The synthesis of homaline. Tetrahedron Lett. 23, 465-468.
    • (1982) Tetrahedron Lett. , vol.23 , pp. 465-468
    • Wasserman, H.H.1    Berger, G.D.2    Cho, K.R.3
  • 23
    • 24044470646 scopus 로고    scopus 로고
    • Organic reactions in aqueous media with a focus on carbon-carbon bond formations: a decade update
    • Li, C. -J. (2005). Organic reactions in aqueous media with a focus on carbon-carbon bond formations: a decade update. Chem. Rev. 105, 3095-3165.
    • (2005) Chem. Rev. , vol.105 , pp. 3095-3165
    • Li, C.-J.1
  • 24
    • 56549128663 scopus 로고    scopus 로고
    • Transition-metal-catalyzed cross-couplings going green:in water at room temperature
    • Lipshutz, B. H., Ghorai, S. (2008). Transition-metal-catalyzed cross-couplings going green:in water at room temperature. Aldrichim. Acta 41, 59-72.
    • (2008) Aldrichim. Acta , vol.41 , pp. 59-72
    • Lipshutz, B.H.1    Ghorai, S.2
  • 25
    • 64549117824 scopus 로고    scopus 로고
    • Organic synthesis "on water"
    • Chanda, A., Fokin, V. V. (2009). Organic synthesis "on water". Chem. Rev. 109, 725-748.
    • (2009) Chem. Rev. , vol.109 , pp. 725-748
    • Chanda, A.1    Fokin, V.V.2
  • 26
    • 70449345895 scopus 로고    scopus 로고
    • Organocatalytic reactions in water
    • Raj, M., Singh, V. K. (2009). Organocatalytic reactions in water. Chem. Commun. 2009, 6687-6703.
    • (2009) Chem. Commun. , vol.2009 , pp. 6687-6703
    • Raj, M.1    Singh, V.K.2
  • 27
    • 78650156215 scopus 로고    scopus 로고
    • Catalysis in aqueous media for the synthesis of drug-like molecules
    • Lombardo, M., Trombini, C. (2010). Catalysis in aqueous media for the synthesis of drug-like molecules. Curr. Opin. Drug Discov. Devel. 13, 717-732.
    • (2010) Curr. Opin. Drug Discov. Devel. , vol.13 , pp. 717-732
    • Lombardo, M.1    Trombini, C.2
  • 28
    • 35548991545 scopus 로고    scopus 로고
    • Gold-catalyzed multicomponent synthesis of aminoindolizines from aldehydes, amines, and alkynes under solvent-free conditions or in water
    • Yan, B., Liu, Y. (2007). Gold-catalyzed multicomponent synthesis of aminoindolizines from aldehydes, amines, and alkynes under solvent-free conditions or in water. Org. Lett. 9, 4323-4326.
    • (2007) Org. Lett. , vol.9 , pp. 4323-4326
    • Yan, B.1    Liu, Y.2
  • 29
    • 0037213014 scopus 로고    scopus 로고
    • InCl3-catalyzed reaction of aromatic amines with cyclic hemiacetals in water: facile synthesis of 1,2,3,4-tetrahydroquinoline derivatives
    • Li, Z., Zhang, J., Li, C.-J. (2003). InCl3-catalyzed reaction of aromatic amines with cyclic hemiacetals in water: facile synthesis of 1,2,3,4-tetrahydroquinoline derivatives. Tetrahedron Lett. 44, 153-156.
    • (2003) Tetrahedron Lett. , vol.44 , pp. 153-156
    • Li, Z.1    Zhang, J.2    Li, C.-J.3
  • 30
    • 43949108252 scopus 로고    scopus 로고
    • Synthesis of substituted 1,2,3,4-tetrahydroquinones by the Povarov reaction. New potentials of the classical reaction
    • Glushkov, V. A., Tolstikov, A. G. (2008). Synthesis of substituted 1,2,3,4-tetrahydroquinones by the Povarov reaction. New potentials of the classical reaction. Russ. Chem. Rev. 77, 137-159.
    • (2008) Russ. Chem. Rev. , vol.77 , pp. 137-159
    • Glushkov, V.A.1    Tolstikov, A.G.2
  • 31
    • 5444270367 scopus 로고
    • 2nd Edition, John Wiley & Sons, Inc. New York
    • Gilman, H., Blatt, A. H. (1941). Organic Syntheses, Collective, Volume I, 2nd Edition, John Wiley & Sons, Inc. New York, pp. 77-80.
    • (1941) Organic Syntheses, Collective , vol.1 , pp. 77-80
    • Gilman, H.1    Blatt, A.H.2
  • 32
    • 0001464392 scopus 로고    scopus 로고
    • A novel 1,5-benzoheteroazepine synthesis via a one-pot coupling-isomerization-cyclocondensation sequence
    • Braun, R. U., Zeitler, K., Müller, T. J. J. (2000). A novel 1,5-benzoheteroazepine synthesis via a one-pot coupling-isomerization-cyclocondensation sequence. Org. Lett. 2, 4181-4184.
    • (2000) Org. Lett. , vol.2 , pp. 4181-4184
    • Braun, R.U.1    Zeitler, K.2    Müller, T.J.J.3
  • 33
    • 34047146356 scopus 로고    scopus 로고
    • A simple, efficient, and green procedure for the 1,4-addition of thiols to conjugated alkenes and alkynes catalyzed by sodium acetate in aqueous medium
    • Ranu, B. C., Mandal, T. (2007). A simple, efficient, and green procedure for the 1,4-addition of thiols to conjugated alkenes and alkynes catalyzed by sodium acetate in aqueous medium. Aust. J. Chem. 60, 223-227.
    • (2007) Aust. J. Chem. , vol.60 , pp. 223-227
    • Ranu, B.C.1    Mandal, T.2
  • 34
    • 44349151476 scopus 로고    scopus 로고
    • 'On water' synthesis of 2,4-diaryl-2,3- dihydro-1,5-benzothiazepines catalysed by sodium dodecyl sulfate (SDS)
    • Sharma, G., Kumar, R., Chakraborti, A. K. (2008). 'On water' synthesis of 2,4-diaryl-2,3- dihydro-1,5-benzothiazepines catalysed by sodium dodecyl sulfate (SDS). Tetrahedron Lett. 49, 4269-4271.
    • (2008) Tetrahedron Lett. , vol.49 , pp. 4269-4271
    • Sharma, G.1    Kumar, R.2    Chakraborti, A.K.3
  • 35
    • 0032222978 scopus 로고    scopus 로고
    • Cycloaddition reaction of benzoheteroazepine: synthesis of 4a,5,6,12-tetrahydro-1H-1,3-oxazino[3,2-d][1,5] benzothiazepin-1-ones and 1H,7H-1,3- oxazino[3,2-d][1,5]benzodiazepin-1-ones
    • Xu, J., Jin, S., Xing, Q. (1998). Cycloaddition reaction of benzoheteroazepine: synthesis of 4a,5,6,12-tetrahydro-1H-1,3-oxazino[3,2-d][1,5] benzothiazepin-1-ones and 1H,7H-1,3- oxazino[3,2-d][1,5]benzodiazepin-1-ones. Phosphorus Sulfur 141, 57-70.
    • (1998) Phosphorus Sulfur , vol.141 , pp. 57-70
    • Xu, J.1    Jin, S.2    Xing, Q.3
  • 36
    • 0032380839 scopus 로고    scopus 로고
    • Preparation and utility of novel water-tolerant higher-order lanthanoid alkoxide complexes as a base catalyst
    • Kamaura, M., Daikai, K., Hanamoto, T., Inanaga, J. (1998). Preparation and utility of novel water-tolerant higher-order lanthanoid alkoxide complexes as a base catalyst. Chem. Lett. 27, 697-698.
    • (1998) Chem. Lett. , vol.27 , pp. 697-698
    • Kamaura, M.1    Daikai, K.2    Hanamoto, T.3    Inanaga, J.4
  • 37
    • 0037463462 scopus 로고    scopus 로고
    • Direct organocatalytic asymmetric Mannich-type reactions in aqueous media: one-pot Mannich-allylation reactions
    • Córdova, A., Barbas, C. F. III. (2003). Direct organocatalytic asymmetric Mannich-type reactions in aqueous media: one-pot Mannich-allylation reactions. Tetrahedron Lett. 44, 1923-1926.
    • (2003) Tetrahedron Lett. , vol.44 , pp. 1923-1926
    • Córdova, A.1    Barbas, C.F.2
  • 38
    • 0037613482 scopus 로고    scopus 로고
    • The first conjugate addition reaction of terminal alkynes catalytic in copper: conjugate addition of alkynes in water
    • Knöpfel, T. F., Carreira, E. M. (2003). The first conjugate addition reaction of terminal alkynes catalytic in copper: conjugate addition of alkynes in water. J. Am. Chem. Soc. 125, 6054-6055.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 6054-6055
    • Knöpfel, T.F.1    Carreira, E.M.2
  • 39
    • 1542268871 scopus 로고    scopus 로고
    • Facile and selective copper-palladium catalyzed addition of terminal alkynes to activated alkynes in water
    • Chen, L., Li, C. -J. (2004). Facile and selective copper-palladium catalyzed addition of terminal alkynes to activated alkynes in water. Tetrahedron Lett. 45, 2771-2774.
    • (2004) Tetrahedron Lett. , vol.45 , pp. 2771-2774
    • Chen, L.1    Li, C.-J.2
  • 40
    • 9144270060 scopus 로고    scopus 로고
    • The first palladium-catalyzed 1,4-addition of terminal alkynes to conjugated enones
    • Chen, L., Li, C. -J. (2004). The first palladium-catalyzed 1,4-addition of terminal alkynes to conjugated enones. Chem. Commun., 2362-2364.
    • (2004) Chem. Commun. , pp. 2362-2364
    • Chen, L.1    Li, C.-J.2
  • 41
    • 0037907937 scopus 로고    scopus 로고
    • An unexpected coupling-isomerization sequence as an entry to novel three-component-pyrazoline syntheses
    • Müller, T. J. J., Ansorge, M., Aktah, D. (2000). An unexpected coupling-isomerization sequence as an entry to novel three-component-pyrazoline syntheses. Angew. Chem. Int. Ed. 39, 1253-1256.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 1253-1256
    • Müller, T.J.J.1    Ansorge, M.2    Aktah, D.3
  • 42
    • 84855663353 scopus 로고    scopus 로고
    • Synthesis of carbo- and heterocycles via coupling-isomerization reactions
    • Review
    • Review: Müller, T. J. J. (2012). Synthesis of carbo- and heterocycles via coupling-isomerization reactions. Synthesis 44, 159-174.
    • (2012) Synthesis , vol.44 , pp. 159-174
    • Müller, T.J.J.1
  • 43
    • 85088232022 scopus 로고
    • The preparation and spectral properties of some monosubstituted 1,3,5-triphenyl-2-pyrazolines
    • Rivett, D. E., Rosevear, J., Wilshire, J. F. K. (1979). The preparation and spectral properties of some monosubstituted 1,3,5-triphenyl-2-pyrazolines. Aust. J. Chem. 32, 1601-1612.
    • (1979) Aust. J. Chem. , vol.32 , pp. 1601-1612
    • Rivett, D.E.1    Rosevear, J.2    Wilshire, J.F.K.3
  • 44
    • 33748735147 scopus 로고    scopus 로고
    • Clean three-step synthesis of 4,5-dihydro-1H-pyrazoles starting from alcohols using polymer supported reagents
    • Haunert, F., Bolli, M. H., Hinzen, B., Ley, S. V. (1998). Clean three-step synthesis of 4,5-dihydro-1H-pyrazoles starting from alcohols using polymer supported reagents. J. Chem. Soc. Perk. Trans. 1, 2235-2238.
    • (1998) J. Chem. Soc. Perk. Trans. , vol.1 , pp. 2235-2238
    • Haunert, F.1    Bolli, M.H.2    Hinzen, B.3    Ley, S.V.4
  • 45
    • 85178410073 scopus 로고
    • Influence of constitution on the transformation of phenylhydrazones of unsaturated compounds into pyrazolines. II
    • von Auwers, K., Kreuder, A. (1925). Influence of constitution on the transformation of phenylhydrazones of unsaturated compounds into pyrazolines. II. Ber. Dtsch. Chem. Ges., 58B, 1974-1986.
    • (1925) Ber. Dtsch. Chem. Ges. , vol.58B , pp. 1974-1986
    • von Auwers, K.1    Kreuder, A.2
  • 46
    • 0034729575 scopus 로고    scopus 로고
    • A novel three-component one-pot pyrimidine synthesis based upon a coupling-isomerization sequence
    • Müller, T. J. J., Braun, R., Ansorge, M. (2000). A novel three-component one-pot pyrimidine synthesis based upon a coupling-isomerization sequence. Org. Lett. 2, 1967-1970.
    • (2000) Org. Lett. , vol.2 , pp. 1967-1970
    • Müller, T.J.J.1    Braun, R.2    Ansorge, M.3
  • 47
    • 3042717901 scopus 로고    scopus 로고
    • Synthesis of multitopic verdazyl radical ligands. Paramagnetic supramolecular synthons
    • Hicks, R. G., Koivisto, B. D., Lemaire, M. T. (2004). Synthesis of multitopic verdazyl radical ligands. Paramagnetic supramolecular synthons. Org. Lett. 6, 1887-1890.
    • (2004) Org. Lett. , vol.6 , pp. 1887-1890
    • Hicks, R.G.1    Koivisto, B.D.2    Lemaire, M.T.3
  • 49
    • 79955703521 scopus 로고    scopus 로고
    • Palladium-catalyzed asymmetric conjugate addition of arylboronic acids to five-, six-, and seven-membered β-substituted cyclic enones: enantioselective construction of all-carbon quaternary stereocenters
    • Kikushima, K., Holder, J. C., Gatti, M., Stoltz, B. M. (2011). Palladium-catalyzed asymmetric conjugate addition of arylboronic acids to five-, six-, and seven-membered β-substituted cyclic enones: enantioselective construction of all-carbon quaternary stereocenters. J. Am. Chem. Soc. 133, 6902-6905.
    • (2011) J. Am. Chem. Soc. , vol.133 , pp. 6902-6905
    • Kikushima, K.1    Holder, J.C.2    Gatti, M.3    Stoltz, B.M.4
  • 50
    • 0037157090 scopus 로고    scopus 로고
    • Enantioselective direct-addition of terminal alkynes to imines catalyzed by copper(I)pybox complex in water and in toluene
    • Wei, C., Li, C.-J. (2002). Enantioselective direct-addition of terminal alkynes to imines catalyzed by copper(I)pybox complex in water and in toluene. J. Am. Chem. Soc. 124, 5638-5639.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 5638-5639
    • Wei, C.1    Li, C.-J.2
  • 51
    • 1942469512 scopus 로고    scopus 로고
    • Cu(I)-catalyzed direct addition and asymmetric addition of terminal alkynes to imines
    • Wei, C., Mague, J. T., Li C. -J. (2004). Cu(I)-catalyzed direct addition and asymmetric addition of terminal alkynes to imines. Proc. Natl. Acad. Sci. U.S.A. 101, 5749-5754.
    • (2004) Proc. Natl. Acad. Sci. U.S.A. , vol.101 , pp. 5749-5754
    • Wei, C.1    Mague, J.T.2    Li, C.-J.3
  • 52
    • 84987393269 scopus 로고
    • An efficient procedure for the Hantzsch dihydropyridine synthesis
    • Watanabe, Y., Shiota, K., Hoshiko, T., Ozaki, S. (1983). An efficient procedure for the Hantzsch dihydropyridine synthesis. Synthesis, 761.
    • (1983) Synthesis , pp. 761
    • Watanabe, Y.1    Shiota, K.2    Hoshiko, T.3    Ozaki, S.4
  • 53
    • 79952439764 scopus 로고    scopus 로고
    • Reaction between N-isocyaniminotriphenylphosphorane, aldimines, Meldrum's aid and water: diastereoselective synthesis of 3,4-disubstituted N-aminopyrrolidine-2,5-diones
    • Adib, M., Ansari, S., Bijanzadeh, H. R. (2011). Reaction between N-isocyaniminotriphenylphosphorane, aldimines, Meldrum's aid and water: diastereoselective synthesis of 3,4-disubstituted N-aminopyrrolidine-2,5-diones. Synlett, 619-622.
    • (2011) Synlett , pp. 619-622
    • Adib, M.1    Ansari, S.2    Bijanzadeh, H.R.3
  • 54
    • 84863717561 scopus 로고    scopus 로고
    • Copper(II) triflate-sodium dodecyl sulfate catalyzed preparation of 1,2-diphenyl-2,3-dihydro-4-pyridones in aqueous acidic medium
    • Lanari, D., Piermatti, O., Pizzo, F., Vaccaro, L. (2012). Copper(II) triflate-sodium dodecyl sulfate catalyzed preparation of 1,2-diphenyl-2,3-dihydro-4-pyridones in aqueous acidic medium. Synthesis 44, 2181-2184.
    • (2012) Synthesis , vol.44 , pp. 2181-2184
    • Lanari, D.1    Piermatti, O.2    Pizzo, F.3    Vaccaro, L.4
  • 55
    • 77950196954 scopus 로고    scopus 로고
    • Spiroheterocycles via regioselective cycloaddition reactions of nitrile oxides with 5-methylene-1H-pyrrol-2(5 h)-ones
    • Beattie, N. J., Francis, C. L., Liepa, A. J., Savage, G. P. (2010). Spiroheterocycles via regioselective cycloaddition reactions of nitrile oxides with 5-methylene-1H-pyrrol-2(5 h)-ones. Aust. J. Chem. 63, 445-451.
    • (2010) Aust. J. Chem. , vol.63 , pp. 445-451
    • Beattie, N.J.1    Francis, C.L.2    Liepa, A.J.3    Savage, G.P.4
  • 57
    • 0242497237 scopus 로고    scopus 로고
    • Practical olefin metathesis in protic media under an air atmosphere
    • Connon, S. J., Rivard, M., Zaja, M., Blechert, S. (2003). Practical olefin metathesis in protic media under an air atmosphere. Adv. Synth. Catal. 345, 572-575.
    • (2003) Adv. Synth. Catal. , vol.345 , pp. 572-575
    • Connon, S.J.1    Rivard, M.2    Zaja, M.3    Blechert, S.4
  • 58
    • 36348949214 scopus 로고    scopus 로고
    • Olefin metathesis in homogeneous aqueous media catalyzed by conventional ruthenium catalysts
    • Binder, J. B., Blank, J. J., Raines, R. T. (2007). Olefin metathesis in homogeneous aqueous media catalyzed by conventional ruthenium catalysts. Org. Lett. 9, 4885-4888.
    • (2007) Org. Lett. , vol.9 , pp. 4885-4888
    • Binder, J.B.1    Blank, J.J.2    Raines, R.T.3
  • 60
    • 0017302121 scopus 로고
    • Synthesis of thymidine oligonucleotides by phosphite triester intermediates
    • Letsinger, R. L., Lunsford, W. B. (1976). Synthesis of thymidine oligonucleotides by phosphite triester intermediates. J. Am. Chem. Soc. 98, 3655-3661.
    • (1976) J. Am. Chem. Soc. , vol.98 , pp. 3655-3661
    • Letsinger, R.L.1    Lunsford, W.B.2
  • 61
    • 33748699338 scopus 로고    scopus 로고
    • Synthetic use of molecular iodine for organic synthesis
    • General review
    • General review: Togo, H., Iida, S. (2006). Synthetic use of molecular iodine for organic synthesis. Synlett, 2159-2175.
    • (2006) Synlett , pp. 2159-2175
    • Togo, H.1    Iida, S.2
  • 62
    • 0033771038 scopus 로고    scopus 로고
    • Aromatization of Hantzsch 1,4-dihydropyridines with I2-MeOH
    • Yadav, J. S., Reddy, B. V. S., Sabitha, G., Reddy, G. S. K. K. (2000). Aromatization of Hantzsch 1,4-dihydropyridines with I2-MeOH. Synthesis, 1532-1534.
    • (2000) Synthesis , pp. 1532-1534
    • Yadav, J.S.1    Reddy, B.V.S.2    Sabitha, G.3    Reddy, G.S.K.K.4
  • 63
    • 33745008887 scopus 로고    scopus 로고
    • The convenient synthesis of benzimidazole derivatives catalyzed by I2 in aqueous media
    • Sun, P., Hu, Z. (2006). The convenient synthesis of benzimidazole derivatives catalyzed by I2 in aqueous media. J. Heterocycl. Chem. 43, 773-775.
    • (2006) J. Heterocycl. Chem. , vol.43 , pp. 773-775
    • Sun, P.1    Hu, Z.2
  • 64
    • 84954665927 scopus 로고
    • 2nd Edition, John Wiley & Sons, Inc. New York
    • Gilman, H., Blatt, A. H. (1941). Organic Syntheses, Collective, Volume I, 2nd Edition, John Wiley & Sons, Inc. New York, pp. 240-241.
    • (1941) Organic Syntheses, Collective , vol.1 , pp. 240-241
    • Gilman, H.1    Blatt, A.H.2
  • 66
    • 0345453464 scopus 로고
    • 2nd Edition, John Wiley & Sons, Inc. New York
    • Gilman, H., Blatt, A. H. (1941). Organic Syntheses, Collective, Volume I, 2nd Edition, John Wiley & Sons, Inc. New York, pp. 101-102.
    • (1941) Organic Syntheses, Collective , vol.1 , pp. 101-102
    • Gilman, H.1    Blatt, A.H.2
  • 68
    • 61349145601 scopus 로고
    • Synthesis of 2,3-dideoxy-D-arabino-heptono-1,4-lactone via a Wittig reaction of unprotected D-arabinose
    • Lyga, J. W. (1992). Synthesis of 2,3-dideoxy-D-arabino-heptono-1,4-lactone via a Wittig reaction of unprotected D-arabinose. Org. Prep. Proced. Int. 24, 73-76.
    • (1992) Org. Prep. Proced. Int. , vol.24 , pp. 73-76
    • Lyga, J.W.1
  • 70
    • 2142811462 scopus 로고    scopus 로고
    • Synthesis of 6I-amino-6I-deoxy-2I-VII,3I-VII-tetradeca-O-methyl-cyclomaltoheptaose
    • Carofiglio, T., Cordioli, M., Fornasier, R., Jicsinszky, L., Tonellato, U. (2004). Synthesis of 6I-amino-6I-deoxy-2I-VII,3I-VII-tetradeca-O-methyl-cyclomaltoheptaose. Carbohydr. Res. 339, 1361-1366.
    • (2004) Carbohydr. Res. , vol.339 , pp. 1361-1366
    • Carofiglio, T.1    Cordioli, M.2    Fornasier, R.3    Jicsinszky, L.4    Tonellato, U.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.