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Volumn 8, Issue 1, 2011, Pages 108-119

Applications of peptide coupling reagents - An update

Author keywords

Carbodiimides; Peptide coupling reagents; Peptides; Phosphonium based reagents; Uranium reagents

Indexed keywords

1 (3 DIMETHYLAMINOPROPYL) 3 ETHYLCARBODIIMIDE; 1 HYDROXYBENZOTRIAZOLE; ACID HALOGENATING REAGENT; BENZOTRIAZOLE 1 YLOXY TRIS(DIMETHYLAMINO)EPHOSPHONIUM HEXAFLUOROPHOSPHATE; BROMO TRIS PYRROLIDINO PHOSPHONIUM HEXAFLUOROPHOSPHATE; CHEMICAL COMPOUND; CHLORIDE; CROSS LINKING REAGENT; CYANAMIDE; FLUORIDE; IMIDAZOLE DERIVATIVE; IMMONIUM; N,N DIISOPROPYLCARBODIIMIDE; ORGANOPHOSPHORUS COMPOUND; OXAZOLONE; PEPTIDE COUPLING REAGENT; PHOSPHONIUM DERIVATIVE; PYRIDINIUM DERIVATIVE; REAGENT; UNCLASSIFIED DRUG; URONIUM;

EID: 79957632173     PISSN: None     EISSN: 0976044X     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (18)

References (152)
  • 10
    • 0000782729 scopus 로고
    • Synthesis of peptides with mixed anhydrides
    • Albertson NF. Synthesis of peptides with mixed anhydrides.Org. React. 1962;12: 157.
    • (1962) Org. React , vol.12 , pp. 157
    • Albertson, N.F.1
  • 11
    • 0002944260 scopus 로고
    • The azide method in peptide synthesis
    • Klausner YS, Bodansky M.The azide method in peptide synthesis. Synthesis.1974:549.
    • (1974) Synthesis , pp. 549
    • Klausner, Y.S.1    Bodansky, M.2
  • 12
    • 0000589494 scopus 로고    scopus 로고
    • Peptide Synthesis via amino acid halides
    • Carpino LA et al. Peptide Synthesis via amino acid halides.Acc.Chem.Res.1996; 29: 268.
    • (1996) Acc.Chem.Res , vol.29 , pp. 268
    • Carpino, L.A.1
  • 15
    • 0029799743 scopus 로고    scopus 로고
    • Protecting group strategies in organic synthesis
    • Schelhaas M, Waldmann H. Protecting group strategies in organic synthesis. Angew.Chem. Int. Ed.1996; 35: 2057.
    • (1996) Angew.Chem. Int. Ed , vol.35
    • Schelhaas, M.1    Waldmann, H.2
  • 20
    • 0007193238 scopus 로고    scopus 로고
    • Chemical Synthesis of Natural Product Peptides: Coupling Methods for the Incorporation of Noncoded Amino Acids into Peptides
    • Humphrey JM, Chamberlin AR. Chemical Synthesis of Natural Product Peptides: Coupling Methods for the Incorporation of Noncoded Amino Acids into Peptides. Chem. Rev. 1997; 97: 2243-2266.
    • (1997) Chem. Rev , vol.97 , pp. 2243-2266
    • Humphrey, J.M.1    Chamberlin, A.R.2
  • 21
    • 85004737474 scopus 로고
    • Coupling reagents in peptide synthesis
    • Klausner YS, Bodanszky M. Coupling reagents in peptide synthesis. Synthesis. 1972: 453-463.
    • (1972) Synthesis , pp. 453-463
    • Klausner, Y.S.1    Bodanszky, M.2
  • 25
    • 0030947731 scopus 로고    scopus 로고
    • Certain amino acids are prone to epimerizationj
    • Romoff TT, Goodman M. Certain amino acids are prone to epimerizationj. Pept. Res. 1997;49:281-292.
    • (1997) Pept. Res , vol.49 , pp. 281-292
    • Romoff, T.T.1    Goodman, M.2
  • 26
    • 0031021498 scopus 로고    scopus 로고
    • Synthesis of the host-selective phytotoxin destruxin B. Avoiding diketopiperazine formation from an N-methyl amino acid dipeptide by use of the Boc-hydrazide derivative
    • Ward DE, Lazny R, Pedras MSC. Synthesis of the host-selective phytotoxin destruxin B. Avoiding diketopiperazine formation from an N-methyl amino acid dipeptide by use of the Boc-hydrazide derivative.Tetrahedron Lett. 1997; 38:339-342.
    • (1997) Tetrahedron Lett , vol.38 , pp. 339-342
    • Ward, D.E.1    Lazny, R.2    Pedras, M.S.C.3
  • 27
    • 85004754595 scopus 로고
    • Side Reactions in Peptide Synthesis
    • Bodanszky M, Martinez J. Side Reactions in Peptide Synthesis.Synthesis.1981: 333-356.
    • (1981) Synthesis , pp. 333-356
    • Bodanszky, M.1    Martinez, J.2
  • 28
    • 0032567305 scopus 로고    scopus 로고
    • Use of Onium Salt- Based Coupling Reagents in Peptide Synthesis
    • Albericio F, Bofill JM, El-Faham A, Kates SA. Use of Onium Salt- Based Coupling Reagents in Peptide Synthesis. J. Org. Chem. 1998;63:9678-9683.
    • (1998) J. Org. Chem , vol.63 , pp. 9678-9683
    • Albericio, F.1    Bofill, J.M.2    El-Faham, A.3    Kates, S.A.4
  • 30
    • 0028050122 scopus 로고
    • BOP, as reagent for mild and efficient preparation of esters
    • Kim MH, Patel DV. BOP, as reagent for mild and efficient preparation of esters.Tetrahedron Lett. 1994; 35: 5603-5606.
    • (1994) Tetrahedron Lett , vol.35 , pp. 5603-5606
    • Kim, M.H.1    Patel, D.V.2
  • 31
    • 0029981008 scopus 로고    scopus 로고
    • Reaction of N-trityl amino acids with BOP: Efficient synthesis of t-butyl esters as well as N-trityl serine- and threonine-β-lactones
    • Sliedregt KM, Schouten A, Kroon J, Liskamp RMJ. Reaction of N-trityl amino acids with BOP: Efficient synthesis of t-butyl esters as well as N-trityl serine- and threonine-β-lactones.Tetrahedron Lett. 1996;37: 4237-4240.
    • (1996) Tetrahedron Lett , vol.37 , pp. 4237-4240
    • Sliedregt, K.M.1    Schouten, A.2    Kroon, J.3    Liskamp, R.M.J.4
  • 32
    • 12444283342 scopus 로고
    • A new method of forming peptide bonds
    • Sheehan JC, Hess GPJ.A new method of forming peptide bonds. J.Am. Chem. Soc. 1955;77:1067-1068.
    • (1955) J.Am. Chem. Soc , vol.77 , pp. 1067-1068
    • Sheehan, J.C.1    Hess, G.P.J.2
  • 33
    • 0014704672 scopus 로고
    • A new method for synthesis of peptides:Activation of carboxyl group with DCC using 1-hydroxy benzotriazoles as additives
    • König W, Geiger R.A new method for synthesis of peptides:activation of carboxyl group with DCC using 1-hydroxy benzotriazoles as additives. Chem. Ber. 1970;103:788-798.
    • (1970) Chem. Ber , vol.103 , pp. 788-798
    • König, W.1    Geiger, R.2
  • 34
    • 0029876180 scopus 로고    scopus 로고
    • Synthesis and Biological Evaluation of C-13 Amide-Linked Paclitaxel (Taxol†) Analogs
    • Chen SH, Farina V, Vyas DM, Doyle TW, Long BH, Fairchild C. Synthesis and Biological Evaluation of C-13 Amide-Linked Paclitaxel (Taxol†) Analogs. J. Org. Chem. 1996;61: 2065-2070.
    • (1996) J. Org. Chem , vol.61 , pp. 2065-2070
    • Chen, S.H.1    Farina, V.2    Vyas, D.M.3    Doyle, T.W.4    Long, B.H.5    Fairchild, C.6
  • 35
    • 0028826185 scopus 로고
    • Macrocyclic Peptide Inhibitors of Serine Proteases. Convergent Total Synthesis of Cyclotheonamides A and B via a Late-Stage Primary Amine Intermediate. Study of Thrombin Inhibition under Diverse Conditions
    • Maryanoff BE, Greco MN, Zhang HC, Andrade Gordon P, Kauffman JA, Nicolaou, KC, et al. Macrocyclic Peptide Inhibitors of Serine Proteases. Convergent Total Synthesis of Cyclotheonamides A and B via a Late-Stage Primary Amine Intermediate. Study of Thrombin Inhibition under Diverse Conditions. J. Am. Chem. Soc. 1995; 117:1225-1239.
    • (1995) J. Am. Chem. Soc , vol.117 , pp. 1225-1239
    • Maryanoff, B.E.1    Greco, M.N.2    Zhang, H.C.3    Andrade Gordon, P.4    Kauffman, J.A.5    Nicolaou, K.C.6
  • 38
    • 0033612107 scopus 로고    scopus 로고
    • The Diisopropylcarbodiimide/1-Hydroxy- 7-azabenzotriazole System: Segment Coupling and Stepwise Peptide Assembly
    • Carpino LA, El-Faham A. The Diisopropylcarbodiimide/1-Hydroxy- 7-azabenzotriazole System: Segment Coupling and Stepwise Peptide Assembly.Tetrahedron. 1999; 55:l6813-6830.
    • (1999) Tetrahedron , vol.55
    • Carpino, L.A.1    El-Faham, A.2
  • 39
    • 0013144515 scopus 로고
    • BDCC and its applications to residue free esterifications,peptide couplings and dehydrations
    • Gibson FS, Park MS, Rapoport H. BDCC and its applications to residue free esterifications,peptide couplings and dehydrations. J. Org. Chem. 1994;59:7503-7507.
    • (1994) J. Org. Chem , vol.59 , pp. 7503-7507
    • Gibson, F.S.1    Park, M.S.2    Rapoport, H.3
  • 40
    • 1342270962 scopus 로고
    • Synthesis of a Heptapeptide Sequence from Bovine Insulin
    • Shields JE, Carpenter FH. Synthesis of a Heptapeptide Sequence from Bovine Insulin. J. Am. Chem. Soc.1961;83:3066-3070.
    • (1961) J. Am. Chem. Soc , vol.83 , pp. 3066-3070
    • Shields, J.E.1    Carpenter, F.H.2
  • 43
    • 0000918830 scopus 로고    scopus 로고
    • Applications of sugar nitrones in synthesis:The total synthesis of(+)-polyoxin
    • Dondoni A, Franco S, Junquera F, Merchán FL, Merino P, tejerot. Applications of sugar nitrones in synthesis:The total synthesis of(+)-polyoxin J. J. Org. Chem. 1997; 62: 5497-5507.
    • (1997) J. J. Org. Chem , vol.62 , pp. 5497-5507
    • Dondoni, A.1    Franco, S.2    Merchán, F.L.3    Merino, P.4    Tejerot5
  • 44
    • 0001082570 scopus 로고
    • Applequist, Poly-β- L-aspartic acid. Synthesis through pentachlorophenyl active ester and conformational studies
    • Kovacs J, Ballina R, Rodin RL, Balasubramanian D, Applequist, Poly-β- L-aspartic acid. Synthesis through pentachlorophenyl active ester and conformational studies J. Am. Chem. Soc. 1965;87:119-120.
    • (1965) J. Am. Chem. Soc , vol.87 , pp. 119-120
    • Kovacs, J.1    Ballina, R.2    Rodin, R.L.3    Balasubramanian, D.4
  • 45
    • 0001012518 scopus 로고    scopus 로고
    • Peptide Coupling in the Presence of Highly Hindered Tertiary aminesj
    • Carpino LA, Ionescu D, El-Faham A. Peptide Coupling in the Presence of Highly Hindered Tertiary aminesj. Org. Chem. 1996; 61: 2460-2465.
    • (1996) Org. Chem , vol.61 , pp. 2460-2465
    • Carpino, L.A.1    Ionescu, D.2    El-Faham, A.3
  • 47
    • 0003068305 scopus 로고
    • Reactions Des Sels De Trisdimethylamino(pseudo) Halophosphonium Sur Les Acides Carboxyliques
    • Castro B, Dormoy JR. Reactions des sels de trisdimethylamino(pseudo) halophosphonium sur les acides carboxyliques.Tetrahedron Lett. 1973:3243-3246.
    • (1973) Tetrahedron Lett , pp. 3243-3246
    • Castro, B.1    Dormoy, J.R.2
  • 50
    • 85007757234 scopus 로고
    • Peptide Coupling Reagents VI1. A Novel, Cheaper Preparation of Benzotriazolyloxytris [dimethylamino] phosphonium Hexafluorophosphate (BOP Reagent)
    • Castro B, Dormoy JR, Dourtoglou B, Evin G, Selve C, Ziebler JC. Peptide Coupling Reagents VI1. A Novel, Cheaper Preparation of Benzotriazolyloxytris [dimethylamino] phosphonium Hexafluorophosphate (BOP Reagent) Synthesis. 1976: 751-752.
    • (1976) Synthesis , pp. 751-752
    • Castro, B.1    Dormoy, J.R.2    Dourtoglou, B.3    Evin, G.4    Selve, C.5    Ziebler, J.C.6
  • 51
    • 0000597775 scopus 로고
    • The reaction of hexamethyl phosphoric triamide (HMPT) with phosphoryl chloride: A reexamination. Application to a novel preparation of BOP reagent for peptide coupling
    • Dormoy JR, Castro B. The reaction of hexamethyl phosphoric triamide (HMPT) with phosphoryl chloride: A reexamination. Application to a novel preparation of BOP reagent for peptide coupling.Tetrahedron Lett. 1979: 3321-3322.
    • (1979) Tetrahedron Lett , pp. 3321-3322
    • Dormoy, J.R.1    Castro, B.2
  • 52
    • 0029795991 scopus 로고    scopus 로고
    • Synthesis of Natural and Modified Trapoxins, Useful Reagents for Exploring Histone Deacetylase Function
    • Taunton J, Collins JL, Schreiber SL. Synthesis of Natural and Modified Trapoxins, Useful Reagents for Exploring Histone Deacetylase Function. J. Am. Chem. Soc.1996; 118: 10412-10422
    • (1996) J. Am. Chem. Soc , vol.118 , pp. 10412-10422
    • Taunton, J.1    Collins, J.L.2    Schreiber, S.L.3
  • 53
    • 0025952348 scopus 로고
    • A new method for rapid solution synthesis of shorter peptides by use ofPyBOP
    • Høeg-Jensen T, Jakobsen M H, Holm A A new method for rapid solution synthesis of shorter peptides by use ofPyBOP. Tetrahedron Lett. 1991;32: 6387-6390.
    • (1991) Tetrahedron Lett , vol.32 , pp. 6387-6390
    • Høeg-Jensen, T.1    Jakobsen, M.H.2    Holm, A.3
  • 54
    • 0026010908 scopus 로고
    • PyBOP® and PyBroP: Two reagents for the difficult coupling of the α,α-dialkyl amino acid, Aib
    • Frérot E, Coste J, Pantaloni A, Dufour MN, Jouin P. PyBOP® and PyBroP: Two reagents for the difficult coupling of the α,α-dialkyl amino acid, Aib. Tetrahedron.1991 47: 259-270.
    • (1991) Tetrahedron , vol.47 , pp. 259-270
    • Frérot, E.1    Coste, J.2    Pantaloni, A.3    Dufour, M.N.4    Jouin, P.5
  • 55
    • 0000791501 scopus 로고
    • N, N'-CARBONYLDIIMIDAZOLE, A NEW REAGENT FOR PEPTIDE SYNTHESIS
    • Anderson GW, Paul R. N, N'-CARBONYLDIIMIDAZOLE, A NEW REAGENT FOR PEPTIDE SYNTHESIS. J. Am. Chem. Soc. 1958; 80: 4423.
    • (1958) J. Am. Chem. Soc , vol.80 , pp. 4423
    • Anderson, G.W.1    Paul, R.2
  • 56
    • 0026645155 scopus 로고
    • Anchoring of Fmoc amino acid to 4-alkoxybenzyl alcohol resin using a new esterification reagent
    • Akaji K, Kuriyama N, Kimura T, Fujiwara Y, Kiso Y Anchoring of Fmoc amino acid to 4-alkoxybenzyl alcohol resin using a new esterification reagent. Tetrahedron Lett. 1992;33: 3177-3180.
    • (1992) Tetrahedron Lett , vol.33 , pp. 3177-3180
    • Akaji, K.1    Kuriyama, N.2    Kimura, T.3    Fujiwara, Y.4    Kiso, Y.5
  • 57
    • 0028956590 scopus 로고
    • Synthesis and biological activities of metabolites of mosapride, a new gastroprokinetic agent
    • Kato S, Morie T, Yoshida N. Synthesis and biological activities of metabolites of mosapride, a new gastroprokinetic agent. Chem. Pharm. Bull. 1995;43: 699-702.
    • (1995) Chem. Pharm. Bull , vol.43 , pp. 699-702
    • Kato, S.1    Morie, T.2    Yoshida, N.3
  • 58
    • 0034670570 scopus 로고    scopus 로고
    • Total Synthesis of Cyclosporin O Both in Solution and in the Solid Phase Using Novel Thiazolium-, Immonium-, and Pyridinium-Type Coupling Reagents: BEMT, BDMP, and BEP
    • Li P, Xu JC. Total Synthesis of Cyclosporin O Both in Solution and in the Solid Phase Using Novel Thiazolium-, Immonium-, and Pyridinium-Type Coupling Reagents: BEMT, BDMP, and BEP.Tetrahedron.2000; 56: 9949-9955.
    • (2000) Tetrahedron , vol.56 , pp. 9949-9955
    • Li, P.1    Xu, J.C.2
  • 60
    • 0342656979 scopus 로고    scopus 로고
    • Total Synthesis of Cyclosporin O Both in Solution and in the Solid Phase Using Novel Thiazolium, Immonium-, and Pyridinium-Type Coupling Reagents: BEMT, BDMP, and BEP
    • Li P, Xu JC Total Synthesis of Cyclosporin O Both in Solution and in the Solid Phase Using Novel Thiazolium, Immonium-, and Pyridinium-Type Coupling Reagents: BEMT, BDMP, and BEP. J. Org. Chem. 2000; 65: 2951-2958.
    • (2000) J. Org. Chem , vol.65 , pp. 2951-2958
    • Li, P.1    Xu, J.C.2
  • 61
    • 0037693678 scopus 로고    scopus 로고
    • Improved Procedure for the Synthesis of Thiazolium-Type Peptide Coupling Reagents: BMTB as a New Efficient Reagent
    • Wischnat R, Rudolph J, Hanke R, Kaese R, May A, Theis H, et al. Improved Procedure for the Synthesis of Thiazolium-Type Peptide Coupling Reagents: BMTB as a New Efficient Reagent.Tetrahedron Lett. 2003;44:4393-4394.
    • (2003) Tetrahedron Lett , vol.44 , pp. 4393-4394
    • Wischnat, R.1    Rudolph, J.2    Hanke, R.3    Kaese, R.4    May, A.5    Theis, H.6
  • 62
    • 0000791684 scopus 로고
    • 1,1'-Carbonylbis(3- methylimidazolium) triflate: An efficient reagent for aminoacylations
    • Saha AK, Schultz P, Rapoport H. 1,1'-Carbonylbis(3- methylimidazolium) triflate: an efficient reagent for aminoacylations J. Am. Chem. Soc.1989; 111: 4856-4859.
    • (1989) J. Am. Chem. Soc , vol.111 , pp. 4856-4859
    • Saha, A.K.1    Schultz, P.2    Rapoport, H.3
  • 63
    • 0013518757 scopus 로고
    • Carboxy Terminus Coupling Using 1,1'- Carbonylbis(3-methylimidazolium triflate) (CBMIT) in the Presence of Cu(II) Salts
    • Gibson FS, Rapoport, H. Carboxy Terminus Coupling Using 1,1'- Carbonylbis(3-methylimidazolium triflate) (CBMIT) in the Presence of Cu(II) Salts. J. Org. Chem. 1995; 60:2615-2617.
    • (1995) J. Org. Chem , vol.60 , pp. 2615-2617
    • Gibson, F.S.1    Rapoport, H.2
  • 64
    • 0015520853 scopus 로고
    • Diphenylphosphoryl azide. New convenient reagent for a modified Curtius reaction and for peptide synthesis
    • Shioiri T, Ninomiya K, Yamada S Diphenylphosphoryl azide. New convenient reagent for a modified Curtius reaction and for peptide synthesis. J. Am. Chem. Soc.1972; 94: 6203-6205.
    • (1972) J. Am. Chem. Soc , vol.94 , pp. 6203-6205
    • Shioiri, T.1    Ninomiya, K.2    Yamada, S.3
  • 66
    • 84985681782 scopus 로고
    • Activation of 2-Alkenoic Acids as Mixed Anhydrides with Diphenylphosphinic Acid for the Formation of Carboxamides
    • Bernasconi S, Comini A, Corbella A, Gariboldi P, Sisti M. Activation of 2-Alkenoic Acids as Mixed Anhydrides with Diphenylphosphinic Acid for the Formation of Carboxamides.Synthesis.1980: 385-387.
    • (1980) Synthesis , pp. 385-387
    • Bernasconi, S.1    Comini, A.2    Corbella, A.3    Gariboldi, P.4    Sisti, M.5
  • 67
    • 0011850124 scopus 로고
    • A New Reagent for Activating Carboxyl Groups; Preparation and Reactions of N,N-Bis[2-oxo-3-oxazolidinyl] phosphorodiamidic Chloride
    • Diago-Meseguer J, Palomo-Coll AL. A New Reagent for Activating Carboxyl Groups; Preparation and Reactions of N,N-Bis[2-oxo-3-oxazolidinyl] phosphorodiamidic Chloride.Synthesis.1980:547-551.
    • (1980) Synthesis , pp. 547-551
    • Diago-Meseguer, J.1    Palomo-Coll, A.L.2
  • 68
    • 33845377031 scopus 로고
    • Bis(2-oxo-3-oxazolidinyl)phosphinic chloride (1) as a coupling reagent for N-alkyl amino acids
    • Tung RD, Rich DH. Bis(2-oxo-3-oxazolidinyl)phosphinic chloride (1) as a coupling reagent for N-alkyl amino acids. J. Am. Chem. Soc.1985; 107: 4342-4343.
    • (1985) J. Am. Chem. Soc , vol.107 , pp. 4342-4343
    • Tung, R.D.1    Rich, D.H.2
  • 70
    • 0030012287 scopus 로고    scopus 로고
    • (-)-Sandramycin: Total Synthesis and Characterization of DNA Binding Properties
    • Boger DL, Chen JH, Saionz KW. (-)-Sandramycin: Total Synthesis and Characterization of DNA Binding Properties. J. Am. Chem. Soc.1996; 118: 1629-1644.
    • (1996) J. Am. Chem. Soc , vol.118 , pp. 1629-1644
    • Boger, D.L.1    Chen, J.H.2    Saionz, K.W.3
  • 71
    • 0020455349 scopus 로고
    • An Extensive Survey by the Use of High Performance Liquid Chromatography on Racemization during the Coupling of Benzyloxycarbonyl-L-phenylalanyl-L-valine with LProline tert-Butyl Ester
    • Takuma S, Hamada Y, Shioiri T. An Extensive Survey by the Use of High Performance Liquid Chromatography on Racemization during the Coupling of Benzyloxycarbonyl-L-phenylalanyl-L-valine with LProline tert-Butyl Ester. Chem. Pharm. Bull.1982; 30: 3147-3153.
    • (1982) Chem. Pharm. Bull , vol.30 , pp. 3147-3153
    • Takuma, S.1    Hamada, Y.2    Shioiri, T.3
  • 72
    • 49549162927 scopus 로고
    • Diethylphosphoryl cyanide. A new reagent for the synthesis of amides
    • Yamada SI, Kasai Y, Shioiri T. Diethylphosphoryl cyanide. A new reagent for the synthesis of amides.Tetrahedron Lett. 1973: 1595-1598.
    • (1973) Tetrahedron Lett , pp. 1595-1598
    • Yamada, S.I.1    Kasai, Y.2    Shioiri, T.3
  • 74
    • 0029079727 scopus 로고
    • A highly efficient synthesis of the anthelmintic cyclooctadepsipeptide PF1022A
    • Scherkenbeck J, Plant A, Harder A, Mencke N. A highly efficient synthesis of the anthelmintic cyclooctadepsipeptide PF1022A.Tetrahedron.1995; 51: 8459-8470.
    • (1995) Tetrahedron , vol.51 , pp. 8459-8470
    • Scherkenbeck, J.1    Plant, A.2    Harder, A.3    Mencke, N.4
  • 75
    • 0025990560 scopus 로고
    • Pentafluorophenyl diphenylphosphinate a new efficient coupling reagent in peptide chemistry
    • Chen S, Xu J. Pentafluorophenyl diphenylphosphinate a new efficient coupling reagent in peptide chemistry. Tetrahedron Lett. 1991; 32:6711-6714.
    • (1991) Tetrahedron Lett , vol.32 , pp. 6711-6714
    • Chen, S.1    Xu, J.2
  • 76
    • 0031597446 scopus 로고    scopus 로고
    • An Efficient Synthesis of Alterobactin A; A Super Siderophore of Marine Origin
    • Deng J, Hamada Y, Shioiri T. An Efficient Synthesis of Alterobactin A; A Super Siderophore of Marine Origin. Synthesis. 1998: 627-638.
    • (1998) Synthesis , pp. 627-638
    • Deng, J.1    Hamada, Y.2    Shioiri, T.3
  • 77
    • 0027305209 scopus 로고
    • 3-dimethylphosphinothioyl-2(3H)-oxazolone (MPTO), a promising new reagent for racemization-free coupling
    • Katoh T, Ueki M. 3-dimethylphosphinothioyl-2(3H)-oxazolone (MPTO), a promising new reagent for racemization-free coupling.Int. J. Pept. Protein Res. 1993; 42:264-269.
    • (1993) Int. J. Pept. Protein Res , vol.42 , pp. 264-269
    • Katoh, T.1    Ueki, M.2
  • 78
    • 37049106538 scopus 로고
    • An 'active ester'- type mixed anhydride method for peptide synthesis. Use of the new reagent, norborn-5-ene-2,3-dicarboximido diphenyl phosphate (NDPP)
    • Kisoy, Miyazaki T, Satomi M, Hiraiwa H, Akita T. An 'active ester'- type mixed anhydride method for peptide synthesis. Use of the new reagent, norborn-5-ene-2,3-dicarboximido diphenyl phosphate (NDPP).J. Chem. Soc., Chem. Commun. 1980: 1029-1030.
    • (1980) J. Chem. Soc., Chem. Commun , pp. 1029-1030
    • Kisoy, M.T.1    Satomi, M.2    Hiraiwa, H.3    Akita, T.4
  • 79
    • 0005983615 scopus 로고
    • A new reagent for the mediation of amide bond formation in peptide synthesis
    • Ramage R, Ashton CP, Hopton D, Parrott MJ. A new reagent for the mediation of amide bond formation in peptide synthesis. Tetrahedron Lett. 1984; 25: 4825-4828.
    • (1984) Tetrahedron Lett , vol.25 , pp. 4825-4828
    • Ramage, R.1    Ashton, C.P.2    Hopton, D.3    Parrott, M.J.4
  • 81
    • 0002799045 scopus 로고
    • A convenient method for the synthesis of carboxamides and peptides by the use of tetrabutylammonium salts
    • Watanabe Y, Mukaiyama T. A convenient method for the synthesis of carboxamides and peptides by the use of tetrabutylammonium salts. Chem. Lett. 1981: 285-288.
    • (1981) Chem. Lett , pp. 285-288
    • Watanabe, Y.1    Mukaiyama, T.2
  • 82
    • 1342334654 scopus 로고
    • One-pot cyclization of a peptide by the use of (5-nitropyridyl)diphenyl phosphinate: The synthesis of cyclic decapeptide gramicidin s
    • Mukaiyama T, Kamekawa K, Watanabe Y. One-pot cyclization of a peptide by the use of (5-nitropyridyl)diphenyl phosphinate: the synthesis of cyclic decapeptide gramicidin s.Chem. Lett.1981:367-1370.
    • (1981) Chem. Lett , pp. 367-1370
    • Mukaiyama, T.1    Kamekawa, K.2    Watanabe, Y.3
  • 84
    • 0000659765 scopus 로고
    • 1,2-Benzisoxazol-3-yl diphenyl phosphate: A new, reactive activating agent for the synthesis of amides, esters, and peptides via condensation J
    • Ueda M, Oikawa H. 1,2-Benzisoxazol-3-yl diphenyl phosphate: a new, reactive activating agent for the synthesis of amides, esters, and peptides via condensation J. Org. Chem. 1985; 50: 760-763.
    • (1985) Org. Chem , vol.50 , pp. 760-763
    • Ueda, M.1    Oikawa, H.2
  • 85
    • 0029918444 scopus 로고    scopus 로고
    • A novel organophosphorus compound as a coupling reagent for peptide synthesis Synth
    • Fan CX, Hao XL, Ye YH. A novel organophosphorus compound as a coupling reagent for peptide synthesis Synth. Commun. 1996; 26:1455-1460.
    • (1996) Commun , vol.26 , pp. 1455-1460
    • Fan, C.X.1    Hao, X.L.2    Ye, Y.H.3
  • 86
    • 0035991443 scopus 로고    scopus 로고
    • Synthesis of cyclopentapeptides and cycloheptapeptides by DEPBT and the influence of some factors on Cyclisation
    • Tang YC, Xie HB, Tian GL,Ye YH. Synthesis of cyclopentapeptides and cycloheptapeptides by DEPBT and the influence of some factors on Cyclisation J. Pept. Res.2002; 60: 95-103.
    • (2002) J. Pept. Res , vol.60 , pp. 95-103
    • Tang, Y.C.1    Xie, H.B.2    Tian, G.L.3    Ye, Y.H.4
  • 87
    • 20344399399 scopus 로고    scopus 로고
    • DEPBT as an efficient coupling reagent for amide bond formation with remarkable resistance to racemization
    • Yun-hua Ye, Haitao Li, Xiahu Jiang. DEPBT as an efficient coupling reagent for amide bond formation with remarkable resistance to racemization. Peptide Science.2004;80:172-178.
    • (2004) Peptide Science , vol.80 , pp. 172-178
    • Yun-Hua, Y.1    Li, H.2    Jiang, X.3
  • 88
    • 0030065343 scopus 로고    scopus 로고
    • Acidic coupling and aminolytic TFA cleavage approaches in a new synthesis of an L-sarcolysin containing antitumor tripeptide ester
    • Weisz I, Roboz J, Bekesi G. Acidic coupling and aminolytic TFA cleavage approaches in a new synthesis of an L-sarcolysin containing antitumor tripeptide ester. Tetrahedron Lett. 1996; 37:563-566.
    • (1996) Tetrahedron Lett , vol.37 , pp. 563-566
    • Weisz, I.1    Roboz, J.2    Bekesi, G.3
  • 89
    • 0028918734 scopus 로고
    • Asymmetric Synthesis of the Volatile Anesthetic 1,2,2,2- Tetrafluoroethyl Chlorofluoromethyl Ether Using a Stereospecific Decarboxylation of Unusual Stereochemical Outcome
    • Rozov LA, Rafalko PW, Evans SM, Brockunier L, Ramig K. Asymmetric Synthesis of the Volatile Anesthetic 1,2,2,2- Tetrafluoroethyl Chlorofluoromethyl Ether Using a Stereospecific Decarboxylation of Unusual Stereochemical Outcome.J. Org. Chem. 1995; 60: 1319-1325.
    • (1995) J. Org. Chem , vol.60 , pp. 1319-1325
    • Rozov, L.A.1    Rafalko, P.W.2    Evans, S.M.3    Brockunier, L.4    Ramig, K.5
  • 90
    • 33845375891 scopus 로고
    • (Fluoren-9-ylmethoxy)carbonyl (Fmoc) amino acid chlorides. Synthesis, characterization, and application to the rapid synthesis of short peptide segments
    • Carpino LA, Cohen BJ, Stephens KE Jr, Sadat-Aalaee Y, Tien JH, Langridge DC. (Fluoren-9-ylmethoxy)carbonyl (Fmoc) amino acid chlorides. Synthesis, characterization, and application to the rapid synthesis of short peptide segments.J. Org. Chem.1986; 51: 3732-3734.
    • (1986) J. Org. Chem , vol.51 , pp. 3732-3734
    • Carpino, L.A.1    Cohen, B.J.2    Stephens Jr., K.E.3    Sadat-Aalaee, Y.4    Tien, J.H.5    Langridge, D.C.6
  • 91
    • 0030962376 scopus 로고    scopus 로고
    • The enantiospecific synthesis of an isoxazoline. A RGD mimic platelet gpiib/iiia antagonist
    • Zhang LH, Chung JC, Costello TD, Valvis I, Ma P, Kauffman S, Ward R. The enantiospecific synthesis of an isoxazoline. A RGD mimic platelet gpiib/iiia antagonist.J. Org. Chem. 1997; 62: 2466-2470.
    • (1997) J. Org. Chem , vol.62 , pp. 2466-2470
    • Zhang, L.H.1    Chung, J.C.2    Costello, T.D.3    Valvis, I.4    Ma, P.5    Kauffman, S.6    Ward, R.7
  • 94
    • 0001452427 scopus 로고
    • Reaction oftert -butyldimethyl-silyl esters with oxalyl chlorides dimethylformamide: Preparation of carboxylic acids under neutral conditions
    • Wissner A, Grudzinskas CV. Reaction oftert -butyldimethyl-silyl esters with oxalyl chlorides dimethylformamide: preparation of carboxylic acids under neutral conditions J. Org. Chem. 1978; 43:3972-3974.
    • (1978) J. Org. Chem , vol.43 , pp. 3972-3974
    • Wissner, A.1    Grudzinskas, C.V.2
  • 95
    • 0000755105 scopus 로고
    • Cyanuric chloride- An useful reagent for converting carboxylic acids into chlorides, esters, anhydrides and peptides
    • Venkataraman K, Wagle D.R. Cyanuric chloride- An useful reagent for converting carboxylic acids into chlorides, esters,anhydrides and peptides. Tetrahedron Lett. 1979; 20:3037-3040.
    • (1979) Tetrahedron Lett , vol.20 , pp. 3037-3040
    • Venkataraman, K.1    Wagle, D.R.2
  • 96
    • 0023640194 scopus 로고
    • 2-Chloro-4,6-dimethoxy-1,3,5-triazine. A new coupling reagent for peptide synthesis
    • Kaminski ZJ. 2-Chloro-4,6-dimethoxy-1,3,5-triazine. A new coupling reagent for peptide synthesis. Synthesis. 1987: 917-920.
    • (1987) Synthesis , pp. 917-920
    • Kaminski, Z.J.1
  • 97
    • 0033041516 scopus 로고    scopus 로고
    • In situ generation of Fmocamino acid chlorides using bis(trichloromethyl) carbonate and its utilization for difficult couplings in solid-phase peptide synthesis
    • Falb E, Yechezkel T, Salitra Y, Gilon C. In situ generation of Fmocamino acid chlorides using bis(trichloromethyl) carbonate and its utilization for difficult couplings in solid-phase peptide synthesis.J. Pept. Res. 1999; 53: 507-517.
    • (1999) J. Pept. Res , vol.53 , pp. 507-517
    • Falb, E.1    Yechezkel, T.2    Salitra, Y.3    Gilon, C.4
  • 99
    • 0037043020 scopus 로고    scopus 로고
    • Triphosgene as highly efficient reagent for the solid-phase coupling of N-alkylated amino acids - total synthesis of cyclosporin O
    • Thern B, Rudolph J, Jung G. Triphosgene as highly efficient reagent for the solid-phase coupling of N-alkylated amino acids - total synthesis of cyclosporin O.Tetrahedron Lett. 2002;43:5013-5016.
    • (2002) Tetrahedron Lett , vol.43 , pp. 5013-5016
    • Thern, B.1    Rudolph, J.2    Jung, G.3
  • 100
    • 33751498929 scopus 로고
    • Tert-Butyloxycarbonyl and benzyloxycarbonyl amino acid fluorides. New, stable rapidacting acylating agents for peptide synthesis
    • Carpino LA, Mansour EME, Sadat-Aalaee D. Tert-Butyloxycarbonyl and benzyloxycarbonyl amino acid fluorides. New, stable rapidacting acylating agents for peptide synthesis. J. Org.Chem. 1991; 56: 2611-2614.
    • (1991) J. Org.Chem , vol.56 , pp. 2611-2614
    • Carpino, L.A.1    Mansour, E.M.E.2    Sadat-Aalaee, D.3
  • 101
    • 0033616097 scopus 로고    scopus 로고
    • Danishefsky. Total Synthesis of 5-N-Acetylardeemin and Amauromine: Practical Routes to Potential MDR Reversal Agents
    • Depew KM, Marsden SP, Zatorska D, Zatorski A, Bornmann WG, Danishefsky. Total Synthesis of 5-N-Acetylardeemin and Amauromine: Practical Routes to Potential MDR Reversal Agents.J. Am. Chem. Soc. 1999;121:11953-11963.
    • (1999) J. Am. Chem. Soc , vol.121 , pp. 11953-11963
    • Depew, K.M.1    Marsden, S.P.2    Zatorska, D.3    Zatorski, A.4    Bornmann, W.G.5
  • 102
    • 0029109071 scopus 로고
    • Tetramethylfluoroformamidinium Hexafluoro phosphate: A Rapid-Acting Peptide Coupling Reagent for Solution and Solid Phase Peptide Synthesis
    • Carpino LA, El-Faham A. Tetramethylfluoroformamidinium Hexafluoro phosphate: A Rapid-Acting Peptide Coupling Reagent for Solution and Solid Phase Peptide Synthesis J. Am. Chem. Soc. 1995; 117:5401-5402.
    • (1995) J. Am. Chem. Soc , vol.117 , pp. 5401-5402
    • Carpino, L.A.1    El-Faham, A.2
  • 103
    • 0032363794 scopus 로고    scopus 로고
    • Bis(tetramethylene)fluoroformamidinium Hexafluorophosphate (BTFFH): A Convenient Coupling Reagent for Solid Phase Peptide Synthesis
    • El-Faham A. Bis(tetramethylene)fluoroformamidinium Hexafluorophosphate (BTFFH): A Convenient Coupling Reagent for Solid Phase Peptide Synthesis.Chem. Lett. 1998: 671-672.
    • (1998) Chem. Lett , pp. 671-672
    • El-Faham, A.1
  • 104
    • 0037450911 scopus 로고    scopus 로고
    • Studies toward a synthesis of C3-epimauritine D: Construction of the macrocycle
    • Kim YA, Shin HN, Park MS, Cho SH, Han SY. Studies toward a synthesis of C3-epimauritine D: construction of the macrocycle. Tetrahedron Lett.2003;44: 2557-2560.
    • (2003) Tetrahedron Lett , vol.44 , pp. 2557-2560
    • Kim, Y.A.1    Shin, H.N.2    Park, M.S.3    Cho, S.H.4    Han, S.Y.5
  • 105
    • 85015356069 scopus 로고
    • Synthetic Methods and Reactions;IV.1 Fluorination of Carboxylic Acids with Cyanuric Fluoride
    • Olah GA, Nojima M, Kerekes I. Synthetic Methods and Reactions;IV.1 Fluorination of Carboxylic Acids with Cyanuric Fluoride. Synthesis. 1973;487-488.
    • (1973) Synthesis , pp. 487-488
    • Olah, G.A.1    Nojima, M.2    Kerekes, I.3
  • 106
    • 0001475687 scopus 로고
    • Amino Acid Fluorides as Reactive Peptide Coupling Reagents
    • Carpino LA, Mansour EME, El-Faham A. Amino Acid Fluorides as Reactive Peptide Coupling Reagents.J. Org. Chem. 1993; 58: 4162-4164.
    • (1993) J. Org. Chem , vol.58 , pp. 4162-4164
    • Carpino, L.A.1    Mansour, E.M.E.2    El-Faham, A.3
  • 107
    • 0028318527 scopus 로고
    • Synthesis of Nalkoxycarbonyl amino acid N-carboxyanhydrides and N,Ndialkoxycarbonyl amino acid fluorides, and the behavior of these amino acid derivatives
    • Savrda J, Chertanova L, Wakselman M. Synthesis of Nalkoxycarbonyl amino acid N-carboxyanhydrides and N,Ndialkoxycarbonyl amino acid fluorides, and the behavior of these amino acid derivatives. Tetrahedron. 1994; 50:5309-5322.
    • (1994) Tetrahedron , vol.50 , pp. 5309-5322
    • Savrda, J.1    Chertanova, L.2    Wakselman, M.3
  • 108
    • 0034692406 scopus 로고    scopus 로고
    • Comparative study of cyanuric fluoride and BOP-Cl carbonyl activators in peptide coupling reactions
    • Kim YA, Han SY. Comparative study of cyanuric fluoride and BOP-Cl carbonyl activators in peptide coupling reactions. Bull. Kor. Chem.Soc. 2000; 21: 943-946.
    • (2000) Bull. Kor. Chem.Soc , vol.21 , pp. 943-946
    • Kim, Y.A.1    Han, S.Y.2
  • 109
    • 0030605880 scopus 로고    scopus 로고
    • Fmoc amino acid fluorides in peptide synthesis - Extension of the method to extremely hindered amino acids
    • Wenschuh H, Beyermann M,Winter R, Blenert M, Ionescu D, Carpino LA. Fmoc amino acid fluorides in peptide synthesis - Extension of the method to extremely hindered amino acids. Tetrahedron Lett. 1996; 37:5483-5486.
    • (1996) Tetrahedron Lett , vol.37 , pp. 5483-5486
    • Wenschuh, H.1    Beyermann, M.2    Winter, R.3    Blenert, M.4    Ionescu, D.5    Carpino, L.A.6
  • 110
    • 49349126081 scopus 로고
    • L'hexafluorophosphate de Obenzotriazolyl- N,N-tetramethyluronium: Un reactif de couplage peptidique nouveau et efficace
    • Dourtoglou V, Ziegler JC, Gross B. L'hexafluorophosphate de Obenzotriazolyl- N,N-tetramethyluronium: Un reactif de couplage peptidique nouveau et efficace. Tetrahedron Lett.1978: 1269-1272.
    • (1978) Tetrahedron Lett , pp. 1269-1272
    • Dourtoglou, V.1    Ziegler, J.C.2    Gross, B.3
  • 111
    • 0021159751 scopus 로고
    • O-Benzotriazolyl-N,N,N′,N′- tetramethyluronium Hexafluorophosphate as Coupling Reagent for the Synthesis of Peptides of Biological Interest
    • Dourtoglou V, Ziegler JC, Gross B. O-Benzotriazolyl-N,N,N′,N′- tetramethyluronium Hexafluorophosphate as Coupling Reagent for the Synthesis of Peptides of Biological Interest. Synthesis. 1984: 572-574.
    • (1984) Synthesis , pp. 572-574
    • Dourtoglou, V.1    Ziegler, J.C.2    Gross, B.3
  • 113
    • 0036462499 scopus 로고    scopus 로고
    • The Uronium/Guanidinium Peptide Coupling Reagents: Finally the True Uronium Salts Angew
    • Carpino LA, Imazumi H, El-Faham A, Ferrer FJ, Zhang C, Lee Y,et al. The Uronium/Guanidinium Peptide Coupling Reagents: Finally the True Uronium Salts Angew. Chem. Int. Ed. 2002;41: 441-445.
    • (2002) Chem. Int. Ed , vol.41 , pp. 441-445
    • Carpino, L.A.1    Imazumi, H.2    El-Faham, A.3    Ferrer, F.J.4    Zhang, C.5    Lee, Y.6
  • 115
    • 0026341239 scopus 로고
    • Sequence-selective recognition of DNA by strand displacement with a thyminesubstituted polyamide
    • Nielsen PE, Egholm M, Berg RH, Buchardt O. Sequence-selective recognition of DNA by strand displacement with a thyminesubstituted polyamide. Science. 1991; 254: 1497-1500.
    • (1991) Science , vol.254 , pp. 1497-1500
    • Nielsen, P.E.1    Egholm, M.2    Berg, R.H.3    Buchardt, O.4
  • 116
    • 0037077790 scopus 로고    scopus 로고
    • Racemization of chiral pnas during solid-phase synthesis: Effect of the coupling conditions on enantiomeric purity
    • Tedeschi T, Corradini R, Marchelli R, Pushl A, Nielsen PE. Racemization of chiral pnas during solid-phase synthesis: effect of the coupling conditions on enantiomeric purity. Tetrahedron: Asymmetry. 2002; 13:1629-1636.
    • (2002) Tetrahedron: Asymmetry , vol.13 , pp. 1629-1636
    • Tedeschi, T.1    Corradini, R.2    Marchelli, R.3    Pushl, A.4    Nielsen, P.E.5
  • 117
    • 0034740937 scopus 로고    scopus 로고
    • Epimerization of peptide nucleic acids analogs during solid-phase synthesis: Optimization of the coupling conditions for increasing the optical purity
    • Corradini R, Sforza S, Dossena A, Palla G, Rocchi R, Filira F, et al. Epimerization of peptide nucleic acids analogs during solid-phase synthesis: optimization of the coupling conditions for increasing the optical purity. Perkin Trans, 2001;1: 2690-2696.
    • (2001) Perkin Trans , vol.1 , pp. 2690-2696
    • Corradini, R.1    Sforza, S.2    Dossena, A.3    Palla, G.4    Rocchi, R.5    Filira, F.6
  • 119
    • 0026598905 scopus 로고
    • A new coupling reagent for peptide synthesis. Benzotriazolvyloxy-bus (pyrroltdino) -carbonium hexaflouorophosphate (BBC)
    • Chen, S.; Xu, J. A new coupling reagent for peptide synthesis. Benzotriazolvyloxy-bus (pyrroltdino) -carbonium hexaflouorophosphate (BBC).Tetrahedron Lett. 1992, 33, 647-650.
    • (1992) Tetrahedron Lett , vol.33 , pp. 647-650
    • Chen, S.1    Xu, J.2
  • 121
    • 0033605816 scopus 로고    scopus 로고
    • Understanding the structure/reactivity of aminium/uronium salts as coupling reagents in peptide synthesis
    • Bofill JM, Fernando A. Understanding the structure/reactivity of aminium/uronium salts as coupling reagents in peptide synthesis.Tetrahedron Lett.1999; 40: 2641-2644.
    • (1999) Tetrahedron Lett , vol.40 , pp. 2641-2644
    • Bofill, J.M.1    Fernando, A.2
  • 123
    • 0030470879 scopus 로고    scopus 로고
    • Cyclization of all-L-Pentapeptides by Means of 1-Hydroxy-7- azabenzotriazole-Derived Uronium and Phosphonium Reagents
    • Ehrlich A, Heyne HU, Winter R, Beyermann M, Haber H, Carpino LA Cyclization of all-L-Pentapeptides by Means of 1-Hydroxy-7- azabenzotriazole-Derived Uronium and Phosphonium Reagents J. Org. Chem. 1996;61: 8831-8838.
    • (1996) J. Org. Chem , vol.61 , pp. 8831-8838
    • Ehrlich, A.1    Heyne, H.U.2    Winter, R.3    Beyermann, M.4    Haber, H.5    Carpino, L.A.6
  • 124
    • 0037198760 scopus 로고    scopus 로고
    • Synthetic Route to the GE3 Cyclodepsipeptide
    • Hale KJ, Lazarides L. Synthetic Route to the GE3 Cyclodepsipeptide. Org. Lett. 2002;4: 1903-1906.
    • (2002) Org. Lett , vol.4 , pp. 1903-1906
    • Hale, K.J.1    Lazarides, L.2
  • 128
    • 0024507836 scopus 로고
    • Synthesis of the cyclodepsipeptide nordidemnin B, a cytotoxic minor product isolated from the sea tunicate Trididemnum cyanophorum
    • Jouin P, Poncet J, Dufour MN, Pantaloni A, Castro B. Synthesis of the cyclodepsipeptide nordidemnin B, a cytotoxic minor product isolated from the sea tunicate Trididemnum cyanophorum. J.Org. Chem. 1989; 54: 617-627.
    • (1989) J.Org. Chem , vol.54 , pp. 617-627
    • Jouin, P.1    Poncet, J.2    Dufour, M.N.3    Pantaloni, A.4    Castro, B.5
  • 130
    • 0023724253 scopus 로고
    • Total synthesis of didemnins- 2,synthesis of didemnins A,Band C
    • Schmidt U, Kroner M, Griesser H. Total synthesis of didemnins- 2,synthesis of didemnins A,Band C. Tetrahedron Lett. 1988; 29:4407-4408.
    • (1988) Tetrahedron Lett , vol.29 , pp. 4407-4408
    • Schmidt, U.1    Kroner, M.2    Griesser, H.3
  • 131
    • 0031045880 scopus 로고    scopus 로고
    • Total synthesis of dehydrodidemnin B. Use ot uronium and phosphonium salt coupling reagents in peptide synthesis in solution
    • Jou G, González I, Albericio F, Lloyd-Williams P, Giralt E. Total synthesis of dehydrodidemnin B. Use ot uronium and phosphonium salt coupling reagents in peptide synthesis in solution. J. Org. Chem. 1997; 62: 354-366.
    • (1997) J. Org. Chem , vol.62 , pp. 354-366
    • Jou, G.1    González, I.2    Albericio, F.3    Lloyd-Williams, P.4    Giralt, E.5
  • 132
    • 41649091460 scopus 로고    scopus 로고
    • Morpholine-Based Immonium and Halogeno amidinium Salts as Coupling Reagents in Peptide synthesis
    • El-Faham A, Albericio F Morpholine-Based Immonium and Halogeno amidinium Salts as Coupling Reagents in Peptide synthesis. J. Org. Chem. 2008; 73: 2731.
    • (2731) J. Org. Chem , vol.2008 , pp. 73
    • El-Faham, A.1    Albericio, F.2
  • 133
    • 70349275493 scopus 로고    scopus 로고
    • Xyma: An Efficient Additive for Peptide Synthesis to Replace the Benzotriazole-Based hobt and hoat with a Lower Risk of Explosion
    • Subirós-Funosas R, Prohens R, Barbas R, El-Faham A, Albericio F. xyma: An Efficient Additive for Peptide Synthesis to Replace the Benzotriazole-Based hobt and hoat with a Lower Risk of Explosion.Chem. Eur. J. 2009;15: 9394.
    • (2009) Chem. Eur. J , vol.15 , pp. 9394
    • Subirós-Funosas, R.1    Prohens, R.2    Barbas, R.3    El-Faham, A.4    Albericio, F.5
  • 134
    • 70349277032 scopus 로고    scopus 로고
    • COMU: A Safer and More Effective Replacement for Benzotriazole-Based Uronium Coupling Reagents
    • El-Faham A, Subirós-Funosas R, Prohens R, Albericio F.COMU: A Safer and More Effective Replacement for Benzotriazole-Based Uronium Coupling Reagents. Chem. Eur. J. 2009; 15: 9404.
    • (2009) Chem. Eur. J , vol.15 , pp. 9404
    • El-Faham, A.1    Subirós-Funosas, R.2    Prohens, R.3    Albericio, F.4
  • 136
    • 0037450911 scopus 로고    scopus 로고
    • Studies toward a synthesis of C3-epimauritine D: Construction of the macrocycle
    • Kimya, Shin HN, Park MS, Cho SH, Han SY. Studies toward a synthesis of C3-epimauritine D: construction of the macrocycle.Tetrahedron Lett.2003;44: 2557-2560.
    • (2003) Tetrahedron Lett , vol.44 , pp. 2557-2560
    • Kimya, S.H.N.1    Park, M.S.2    Cho, S.H.3    Han, S.Y.4
  • 137
    • 33947459491 scopus 로고
    • Acylalkylcarbonates as acylating agents for the synthesis of peptides
    • Vaughan JR. Acylalkylcarbonates as acylating agents for the synthesis of peptides.J. Am. Chem. Soc. 1951; 73: 3547.
    • (1951) J. Am. Chem. Soc , vol.73 , pp. 3547
    • Vaughan, J.R.1
  • 141
    • 0029045120 scopus 로고
    • A new approach to the asymmetric synthesis of carbacephams
    • Berrien JF, Billion MA, Husson HP. A new approach to the asymmetric synthesis of carbacephams. J. Org. Chem. 1995; 60: 2922-2924.
    • (1995) J. Org. Chem , vol.60 , pp. 2922-2924
    • Berrien, J.F.1    Billion, M.A.2    Husson, H.P.3
  • 142
    • 0034612979 scopus 로고    scopus 로고
    • 1-Ethyl 2-halopyridinium salts, highly efficient coupling reagents for hindered peptide synthesis both in solution and the solid-phase
    • Li P, Xu JC. 1-Ethyl 2-halopyridinium salts, highly efficient coupling reagents for hindered peptide synthesis both in solution and the solid-phase.Tetrahedron. 2000; 56: 8119-8131.
    • (2000) Tetrahedron , vol.56 , pp. 8119-8131
    • Li, P.1    Xu, J.C.2
  • 143
    • 0034335649 scopus 로고    scopus 로고
    • 2-Bromo-1-ethyl Pyridinium Tetrafluoroborate (BEP): A Powerful Coupling Reagent for N-Methylated Peptide Synthesis
    • Li P, Xu JC. 2-Bromo-1-ethyl Pyridinium Tetrafluoroborate (BEP): A Powerful Coupling Reagent for N-Methylated Peptide Synthesis. Chem. Lett. 2000:204-205.
    • (2000) Chem. Lett , pp. 204-205
    • Li, P.1    Xu, J.C.2
  • 144
    • 0032887355 scopus 로고    scopus 로고
    • Di-tert-Butyl Dicarbonate: A Novel Reagent for the Efficient Synthesis of Dipeptides Under Mild Conditions
    • Mohapatra DK, Datta A. Di-tert-Butyl Dicarbonate: A Novel Reagent for the Efficient Synthesis of Dipeptides Under Mild Conditions J. Org. Chem. 1999;64:6879-6880.
    • (1999) J. Org. Chem , vol.64 , pp. 6879-6880
    • Mohapatra, D.K.1    Datta, A.2
  • 145
    • 0033963499 scopus 로고    scopus 로고
    • 4-(4,6-Dimethoxy- 1,3,5-triazin-2-yl)-4-methyl-morpholinium chloride. A Valuable Alternative to pybop for Solid Phase Peptide Synthesis
    • Falchi A., Giacomelli G, Porcheddu A, Taddei M. 4-(4,6-Dimethoxy- 1,3,5-triazin-2-yl)-4-methyl-morpholinium chloride. A Valuable Alternative to pybop for Solid Phase Peptide Synthesis. Synlett.2000: 275-277.
    • (2000) Synlett , pp. 275-277
    • Falchi, A.1    Giacomelli, G.2    Porcheddu, A.3    Taddei, M.4
  • 148
    • 0032211333 scopus 로고    scopus 로고
    • Synthesis and application of a novel coupling reagent, ethyl 1-hydroxy- 1H-1,2,3-triazole-4-carboxylate
    • Jiang L, Davision A, Tennant G, Ramage R. Synthesis and application of a novel coupling reagent, ethyl 1-hydroxy- 1H-1,2,3-triazole-4-carboxylate. Tetrahedron. 1998; 54:14233-14254.
    • (1998) Tetrahedron , vol.54 , pp. 14233-14254
    • Jiang, L.1    Davision, A.2    Tennant, G.3    Ramage, R.4
  • 149
    • 0041902735 scopus 로고    scopus 로고
    • Tetramethylfluoroformamidinium hexafluorophosphate: A rapid-acting peptide coupling reagent for solution and solid phase peptide synthesis
    • Carpino LA, Ionescu D, El-Faham A Beyermann M, Henklein P, Hanay C Tetramethylfluoroformamidinium hexafluorophosphate: a rapid-acting peptide coupling reagent for solution and solid phase peptide synthesis. Org.Lett. 2003; 5: 975-977.
    • (2003) Org.Lett , vol.5 , pp. 975-977
    • Carpino, L.A.1    Ionescu, D.2    El-Faham, A.3    Beyermann, M.4    Henklein, P.5    Hanay, C.6
  • 150
    • 0032928186 scopus 로고    scopus 로고
    • A racemization-free coupling method for peptides having Nmethylamino acids at the carboxy-termini
    • Nishiyama Y, Tanaka M, Saito S, Ishizuka S, Mori T, Kurita, K. A racemization-free coupling method for peptides having Nmethylamino acids at the carboxy-termini.Chem. Pharm. Bull. 1999; 47: 576-578
    • (1999) Chem. Pharm. Bull , vol.47 , pp. 576-578
    • Nishiyama, Y.1    Tanaka, M.2    Saito, S.3    Ishizuka, S.4    Mori, T.5    Kurita, K.6
  • 151
    • 0035842149 scopus 로고    scopus 로고
    • O-(7-Azabenzotriazol-1-yl)-1,1,3,3- Tetra methyluronium hexafluorophosphate--1-hydroxy-7- azabenzotriazole-copper(II) chloride: A promising epimerizationfree segment coupling system for peptide synthesis
    • Nishiyama Y, Ishizuka S, Kurita K.O-(7-Azabenzotriazol-1-yl)-1,1,3,3- Tetra methyluronium hexafluorophosphate--1-hydroxy-7- azabenzotriazole-copper(II) chloride: a promising epimerizationfree segment coupling system for peptide synthesis. Tetrahedron Lett.2001; 42: 8789-8791
    • (2001) Tetrahedron Lett , vol.42 , pp. 8789-8791
    • Nishiyama, Y.1    Ishizuka, S.2
  • 152
    • 0035063449 scopus 로고    scopus 로고
    • Cu(obt)2 and Cu(oat)2, copper(II)-based racemization suppressors ready for use in fully automated solid-phase peptide synthesis
    • Van den Nest W, Yuval S, Albericio F. Cu(obt)2 and Cu(oat)2, copper(II)-based racemization suppressors ready for use in fully automated solid-phase peptide synthesis. J. Pept. Sci. 2001;7: 115-120.
    • (2001) J. Pept. Sci , vol.7 , pp. 115-120
    • van den Nest, W.1    Yuval, S.2    Albericio, F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.