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Volumn 3, Issue 3, 2011, Pages 1102-1118

Methods for synthesis of oxazolones: A review

Author keywords

Carbodiimide; Erlenmeyer plochl reaction; Intramolecular diels alder reaction; Photosensitive

Indexed keywords

1 (2 CHLOROACETYL) 5 METHYL 5 (4 PHENYLCYCLOHEXYL)DIHYDROPYRANO[3,2 D]OXAZOLE 2,6 DIONE; 1 [1 [2 (2,4 DICHLOROPHENYL) 5 OXOOXAZOL 4 YLIDENE]PROPYL]AZETIDINE 2 CARBOXYLIC ACID[1 CARBAMOYL 2 (4 HYDROXYPHENYL)ETHYL]AMIDE; 2 (2 CHLORO 4 NITROPHENYL) 4 FURAN 2 YLMETHYLENE 4H OXAZOL 5 ONE; 2 (4 NITROPHENYL) 4 [4 (1,4,7,10 TETRAOXA 13 AZACYCLOPENTADEC 13 YL)BENZYLIDENE] 4H OXAZOL 5 ONE; 2 METHYL 4 (4 NITROBENZYLIDENE) 4H OXAZOL 5 ONE; 2 OXOBENZOOXAZOL 3 YL) ACETIC ACID (4 CHLOROBENZYLIDENE)HYDRAZIDE; 2 PHENYL 4 (3 PHENYLALLYLIDENE) 4H OXAZOL 5 ONE; 2 PHENYL 5(4H) OXAZOLONE; 4 (3 CHLOROBENZYLIDENE) 2 PHENYL 4H OXAZOL 5 ONE; 4 [3 (4 CHLOROPHENYL) 1 PHENYL 1H PYRAZOL 4 YLMETHYLENE] 2 PHENYL 4H OXAZOL 5 ONE; 4 BENZYLIDENE 2 PHENYL 4H OXAZOL 5 ONE; 4 METHYLOXAZOL 2 ONE; 5 METHYL 1 PHENYL 6 OXA 4 AZASPIRO[2.4]HEPT 4 EN 7 ONE; 5 METHYL 3H BENZOOXAZOL 2 ONE; ALPHA AMINO ACID; BENZALDEHYDE; CARBON DIOXIDE; DIKETONE; GLYCINE; GUANINE; HYDROXYL RADICAL; INDOLE DERIVATIVE; NUCLEOPHILE; OXAZOLE DERIVATIVE; OXAZOLONE; PYRIDINE DERIVATIVE; RUTHENIUM; SAMARIUM; THREONINE; UNCLASSIFIED DRUG; ZINC OXIDE;

EID: 79961152762     PISSN: None     EISSN: 09744290     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (36)

References (74)
  • 2
    • 0013474892 scopus 로고
    • The Erlenmeyer synthesis of amino-acids
    • Lamb J., and Robson W., The Erlenmeyer synthesis of amino-acids, Biochemical Journal, 1931, 25, 1231-1236.
    • (1931) Biochemical Journal , vol.25 , pp. 1231-1236
    • Lamb, J.1    Robson, W.2
  • 3
    • 0041968924 scopus 로고
    • Physical characteristics and polarographic reduction mechanism of some oxazolones
    • Ismail M.I., Physical characteristics and polarographic reduction mechanism of some oxazolones, Canadian Journal of Chemistry, 1991, 69, 1886-1892.
    • (1991) Canadian Journal of Chemistry , vol.69 , pp. 1886-1892
    • Ismail, M.I.1
  • 4
    • 0032564536 scopus 로고    scopus 로고
    • Photoinduced one pot transformation of 2- phenyl-4-ethylidene-5(4H)-oxazolone and allylic alcohols to γ, δ-unsaturated N-benzoyl amides
    • Park B.S., Min Oh C., Chun K.H., and Lee J.O., Photoinduced one pot transformation of 2- phenyl-4-ethylidene-5(4H)-oxazolone and allylic alcohols to γ, δ-unsaturated N-benzoyl amides, Tetrahedron Letters, 1998, 39, 9711-9714.
    • (1998) Tetrahedron Letters , vol.39 , pp. 9711-9714
    • Park, B.S.1    Min, O.C.2    Chun, K.H.3    Lee, J.O.4
  • 5
    • 67649872667 scopus 로고    scopus 로고
    • Spectral properties of novel 1,3- oxazol-5(4H)-ones with substituted benzylidene and phenyl rings
    • Palcut M., Spectral properties of novel 1,3- oxazol-5(4H)-ones with substituted benzylidene and phenyl rings, Acta Chimica Slovenica, 2009, 56, 362-368.
    • (2009) Acta Chimica Slovenica , vol.56 , pp. 362-368
    • Palcut, M.1
  • 6
    • 0030986896 scopus 로고    scopus 로고
    • Resolution of racemic carboxylic acid derivatives by Ti-TADDOLate mediated esterification reactions: A general method for the preparation of enantiopure compounds
    • Seebach D., Jaeschke G., Gottwald K., Matsuda K., Formisano R., and Chaplin D.A., Resolution of racemic carboxylic acid derivatives by Ti-TADDOLate mediated esterification reactions: a general method for the preparation of enantiopure compounds, Tetrahedron, 1997, 53, 7539-7556.
    • (1997) Tetrahedron , vol.53 , pp. 7539-7556
    • Seebach, D.1    Jaeschke, G.2    Gottwald, K.3    Matsuda, K.4    Formisano, R.5    Chaplin, D.A.6
  • 7
    • 0033556055 scopus 로고    scopus 로고
    • Ring opening with kinetic resolution of azlactones by Ti- TADDOLates
    • Gottwald K., and Seebach D., Ring opening with kinetic resolution of azlactones by Ti- TADDOLates, Tetrahedron, 1999, 55, 723-738.
    • (1999) Tetrahedron , vol.55 , pp. 723-738
    • Gottwald, K.1    Seebach, D.2
  • 8
    • 22544463937 scopus 로고    scopus 로고
    • Synthetic utility of five-membered heterocycles-chiral functionalization and applications
    • Matsunaga H., Ishizuka T., and Kunieda T., Synthetic utility of five-membered heterocycles-chiral functionalization and applications, Tetrahedron, 2005, 61, 8073-8094.
    • (2005) Tetrahedron , vol.61 , pp. 8073-8094
    • Matsunaga, H.1    Ishizuka, T.2    Kunieda, T.3
  • 9
    • 0037399052 scopus 로고    scopus 로고
    • Kinetic study of alkaline induced hydrolysis of the skeletal muscle relaxant chlorzoxazone using ratio spectra first derivative Spectrophotometry
    • Ellaithy M.M., El-Ragehy N.A., and El- Ghobashy M.A., Kinetic study of alkaline induced hydrolysis of the skeletal muscle relaxant chlorzoxazone using ratio spectra first derivative Spectrophotometry, IL Farmaco, 2003, 58, 337-342.
    • (2003) IL Farmaco , vol.58 , pp. 337-342
    • Ellaithy, M.M.1    El-Ragehy, N.A.2    El-Ghobashy, M.A.3
  • 10
    • 34447267965 scopus 로고    scopus 로고
    • Aktay G., and Ozalp M., 1- Acylthiosemicarbazides, 1,2,4-triazole-5(4H)- thiones,1,3,4-thiadiazoles and hydrazones containing 5-methyl-2-benzoxazolinones: Synthesis, analgesic-anti-inflammatory and antimicrobial activities
    • Goksen U.S., Kelekci N.G., Goktas O., Koysal Y., Kilic E., Isik S., Aktay G., and Ozalp M., 1- Acylthiosemicarbazides, 1,2,4-triazole-5(4H)- thiones,1,3,4-thiadiazoles and hydrazones containing 5-methyl-2-benzoxazolinones: synthesis, analgesic-anti-inflammatory and antimicrobial activities, Bioorganic & Medicinal Chemistry, 2007, 15, 5738-5751.
    • (2007) Bioorganic & Medicinal Chemistry , vol.15 , pp. 5738-5751
    • Goksen, U.S.1    Kelekci, N.G.2    Goktas, O.3    Koysal, Y.4    Kilic, E.5    Isik, S.6
  • 11
    • 17044441347 scopus 로고    scopus 로고
    • Anti-nociceptive and anti-inflammatory activity of some (2- benzoxazolone-3-yl and 2-benzothiazolone-3- yl) acetic acid derivatives
    • Dogruer D.S., Unlu S., Sahin M.F., and Yesilada E., Anti-nociceptive and anti-inflammatory activity of some (2- benzoxazolone-3-yl and 2-benzothiazolone-3- yl) acetic acid derivatives, IL Farmaco, 1998, 53, 80-84.
    • (1998) IL Farmaco , vol.53 , pp. 80-84
    • Dogruer, D.S.1    Unlu, S.2    Sahin, M.F.3    Yesilada, E.4
  • 12
    • 67651120410 scopus 로고    scopus 로고
    • Zinc Oxide (ZnO): An efficient catalyst for the synthesis of 4- arylmethylidene-2-phenyl-5-(4H)-oxazolones having antimicrobial activity
    • Pasha M.A., Jayashankara V.P., Venugopala K.N., and Rao G.K., Zinc Oxide (ZnO): an efficient catalyst for the synthesis of 4- arylmethylidene-2-phenyl-5-(4H)-oxazolones having antimicrobial activity, Journal of Pharmacology and Toxicology, 2007, 2, 264-270.
    • (2007) Journal of Pharmacology and Toxicology , vol.2 , pp. 264-270
    • Pasha, M.A.1    Jayashankara, V.P.2    Venugopala, K.N.3    Rao, G.K.4
  • 14
    • 78650998155 scopus 로고
    • The antibacterial activity of some synthetic compounds related to penicillin
    • Brownlee G., and Woodbine M., The antibacterial activity of some synthetic compounds related to penicillin, British Journal of Pharmacology, 1948, 3, 305-308.
    • (1948) British Journal of Pharmacology , vol.3 , pp. 305-308
    • Brownlee, G.1    Woodbine, M.2
  • 15
    • 0035540414 scopus 로고    scopus 로고
    • New novel synthesis and antibacterial activity of 1- (substituted phenyl)-2-phenyl-4-(3'-halo, 4'- hydroxy 5'-methoxy benzylidene)-imidazole-5- ones
    • Siddiqui S.A., Bhusare S.R., Jarikote D.V., Pawar R.P., and Vibhute Y.B., New novel synthesis and antibacterial activity of 1- (substituted phenyl)-2-phenyl-4-(3'-halo, 4'- hydroxy 5'-methoxy benzylidene)-imidazole-5- ones, Bulletin of the Korean Chemical Society, 2001, 22, 1033-1036.
    • (2001) Bulletin of the Korean Chemical Society , vol.22 , pp. 1033-1036
    • Siddiqui, S.A.1    Bhusare, S.R.2    Jarikote, D.V.3    Pawar, R.P.4    Vibhute, Y.B.5
  • 17
    • 79961144680 scopus 로고    scopus 로고
    • Pesticidal effects of some imidazolidine and oxazolone derivatives
    • Abdel-Aty A.S., Pesticidal effects of some imidazolidine and oxazolone derivatives, World Journal of Agricultural Sciences, 2009, 5, 105-113.
    • (2009) World Journal of Agricultural Sciences , vol.5 , pp. 105-113
    • Abdel-Aty, A.S.1
  • 18
    • 42049105094 scopus 로고    scopus 로고
    • Microwave assisted improved method for the synthesis of pyrazole containing 2,4,- disubstitute oxazole-5-one and their antimicrobial activity
    • Argade N.D., Kalrale B.K., and Gill C.H., Microwave assisted improved method for the synthesis of pyrazole containing 2,4,- disubstitute oxazole-5-one and their antimicrobial activity, European Journal of Chemistry, 2008, 5, 120-129.
    • (2008) European Journal of Chemistry , vol.5 , pp. 120-129
    • Argade, N.D.1    Kalrale, B.K.2    Gill, C.H.3
  • 19
    • 33751335837 scopus 로고    scopus 로고
    • Indolocarbazole natural products: Occurrence, biosynthesis and biological activity
    • Sanchez C., Mendez C., and Salas J.A., Indolocarbazole natural products: occurrence, biosynthesis and biological activity, Natural Product Reports, 2006, 23, 1007-1045.
    • (2006) Natural Product Reports , vol.23 , pp. 1007-1045
    • Sanchez, C.1    Mendez, C.2    Salas, J.A.3
  • 20
    • 79961163915 scopus 로고    scopus 로고
    • Part I. A 2- nitroimidazole indocyanine green dye derivative tumor imaging agent. Part II. A dichlorination-reductive-dechlorination route to N-acetyl-2-oxazolone. Part III. Intramolecular Diels-Alder approach to the synthesis of pancratistatin
    • AAT 3289509
    • Gaenzler and Corbo F., Part I. A 2- nitroimidazole indocyanine green dye derivative tumor imaging agent. Part II. A dichlorination-reductive-dechlorination route to N-acetyl-2-oxazolone. Part III. Intramolecular Diels-Alder approach to the synthesis of pancratistatin, ProQuest and Dissertations Theses, 2007, AAT 3289509, pp. 163.
    • (2007) ProQuest and Dissertations Theses , pp. 163
    • Gaenzler1    Corbo, F.2
  • 21
    • 0033053280 scopus 로고    scopus 로고
    • Inhibition of human immunodeficiency virus type (HIV-1) replication by some diversely functionalized spirocyclopropyl derivatives
    • Witvrouw M., Pannecouque C., Clercq E.D., Fernandez-Alvarez, E. and Marco J.L., Inhibition of human immunodeficiency virus type (HIV-1) replication by some diversely functionalized spirocyclopropyl derivatives, Arch. Pharm. Pharm. Med. Chem, 1999, 352, 163-166.
    • (1999) Arch. Pharm. Pharm. Med. Chem , vol.352 , pp. 163-166
    • Witvrouw, M.1    Pannecouque, C.2    Clercq, E.D.3    Fernandez-Alvarez, E.4    Marco, J.L.5
  • 23
    • 77956091918 scopus 로고    scopus 로고
    • Facile synthesis of acyclic analogues of carbocyclic nucleoside as potential anti-HIV prodrug
    • Siddiqui I R., Singh P.K., Srivastava V., and Singh J., Facile synthesis of acyclic analogues of carbocyclic nucleoside as potential anti-HIV prodrug, Indian Journal of Chemistry 2010, 49B, 512-520.
    • (2010) Indian Journal of Chemistry , vol.49 B , pp. 512-520
    • Siddiqui, I.R.1    Singh, P.K.2    Srivastava, V.3    Singh, J.4
  • 25
    • 0036913298 scopus 로고    scopus 로고
    • Simple one-step syntheses of heterocyclic systems from (4Z)-2-phenyl-4- (thien-2-ylmethylene)-1,3(4H)-oxazol-5-one
    • Madkour H.M.F., Simple one-step syntheses of heterocyclic systems from (4Z)-2-phenyl-4- (thien-2-ylmethylene)-1,3(4H)-oxazol-5-one, Chemical Papers, 2002, 56, 313-319.
    • (2002) Chemical Papers , vol.56 , pp. 313-319
    • Madkour, H.M.F.1
  • 27
    • 58149234164 scopus 로고    scopus 로고
    • Dodecatungstophosphoric acid (H3PW12O40), samarium and ruthenium (i{cyrillic, ukrainian}i{cyrillic, ukrainian}i{cyrillic, ukrainian}) chloride catalyzed synthesis of unsaturated 2-phenyl- 5(4H)-oxazolone derivatives under solvent-free conditions
    • Tikdari A.M., Fozooni S., and Hamidian H., Dodecatungstophosphoric acid (H3PW12O40), samarium and ruthenium (i{cyrillic, ukrainian}i{cyrillic, ukrainian}i{cyrillic, ukrainian}) chloride catalyzed synthesis of unsaturated 2-phenyl- 5(4H)-oxazolone derivatives under solvent-free conditions, Molecules, 2008, 13, 3246-3252.
    • (2008) Molecules , vol.13 , pp. 3246-3252
    • Tikdari, A.M.1    Fozooni, S.2    Hamidian, H.3
  • 29
    • 79961136204 scopus 로고
    • United States Patent, Patent No: US 4698353, Oct
    • Schnettler et al., Cardiotonic heterocyclic oxazolones, United States Patent, Patent No: US 4698353, Oct. 6, 1987.
    • (1987) Cardiotonic Heterocyclic Oxazolones , pp. 6
    • Schnettler1
  • 30
    • 0037034802 scopus 로고    scopus 로고
    • Intramolecular Diels-Alder reactions of N-substituted oxazolones
    • Fearnley S.P., and Market E., Intramolecular Diels-Alder reactions of N-substituted oxazolones, Chemical Communications, 2002, 438-439.
    • (2002) Chemical Communications , pp. 438-439
    • Fearnley, S.P.1    Market, E.2
  • 32
    • 34548800411 scopus 로고    scopus 로고
    • Photophysical characterization of fluorescent oxazol-5-one derivatives in PVC and their application as biosensors in the detection of ACh and AChE inhibitor: Donepezil
    • Ozturk G., Alp S., and Timur S., Photophysical characterization of fluorescent oxazol-5-one derivatives in PVC and their application as biosensors in the detection of ACh and AChE inhibitor: donepezil, Dyes and Pigments, 2008, 76, 792-798.
    • (2008) Dyes and Pigments , vol.76 , pp. 792-798
    • Ozturk, G.1    Alp, S.2    Timur, S.3
  • 33
    • 0030006940 scopus 로고    scopus 로고
    • Photodecarbonylation of 2-phenyl-4- alkylidene-5(4H)-oxazolones
    • Jung B., Kim H., and Park B.S., Photodecarbonylation of 2-phenyl-4- alkylidene-5(4H)-oxazolones, Tetrahedron Letters, 1996, 37, 4019-4022.
    • (1996) Tetrahedron Letters , vol.37 , pp. 4019-4022
    • Jung, B.1    Kim, H.2    Park, B.S.3
  • 34
    • 34548484788 scopus 로고    scopus 로고
    • Synthesis and spectroscopic properties of new 5-oxazolone derivatives containing an N-phenyl-aza-15- crown-5 moiety
    • Ozturk G., Alp S., and Ergun Y., Synthesis and spectroscopic properties of new 5-oxazolone derivatives containing an N-phenyl-aza-15- crown-5 moiety, Tetrahedron Letters, 2007, 48, 7347-7350.
    • (2007) Tetrahedron Letters , vol.48 , pp. 7347-7350
    • Ozturk, G.1    Alp, S.2    Ergun, Y.3
  • 35
    • 33746963563 scopus 로고    scopus 로고
    • Fluorescence emission studies of 4-(2- furylmethylene)-2-phenyl-5-oxazolone embedded in polymer thin film and detection of Fe3+ ion
    • Ozturk G., Alp S., and Ertekin K., Fluorescence emission studies of 4-(2- furylmethylene)-2-phenyl-5-oxazolone embedded in polymer thin film and detection of Fe3+ ion, Dyes and Pigments, 2007, 72, 150-156.
    • (2007) Dyes and Pigments , vol.72 , pp. 150-156
    • Ozturk, G.1    Alp, S.2    Ertekin, K.3
  • 36
    • 77249146342 scopus 로고    scopus 로고
    • Synthesis and study of nonlinear optical properties of 4-substituted benzylidene- 2-phenyl oxazol-5-ones by Z-scan technique
    • Murthy Y.L.N., Christophera V., Prasad U.V., Bisht P.B., Ramanaih D.V., Kalanoor B.S., and Ali S.A., Synthesis and study of nonlinear optical properties of 4-substituted benzylidene- 2-phenyl oxazol-5-ones by Z-scan technique, Synthetic Metals, 2010, 160, 535-539.
    • (2010) Synthetic Metals , vol.160 , pp. 535-539
    • Murthy, Y.L.N.1    Christophera, V.2    Prasad, U.V.3    Bisht, P.B.4    Ramanaih, D.V.5    Kalanoor, B.S.6    Ali, S.A.7
  • 37
    • 2342568247 scopus 로고    scopus 로고
    • A novel variable selection and modeling method based on the prediction for QSAR of cyclooxygenase-2 inhibition by thiazolone and oxazolone series
    • Liu S.S., Cui S.H., Shi Y.Y., and Wang L.S., A novel variable selection and modeling method based on the prediction for QSAR of cyclooxygenase-2 inhibition by thiazolone and oxazolone series, Internet Electronic Journal of Molecular Design, 2002, 1, 610-619.
    • (2002) Internet Electronic Journal of Molecular Design , vol.1 , pp. 610-619
    • Liu, S.S.1    Cui, S.H.2    Shi, Y.Y.3    Wang, L.S.4
  • 38
    • 34447340519 scopus 로고    scopus 로고
    • The 'azirine/oxazolone method' in peptaibol synthesis: Preparation of a derivative of trichotoxin A-50 (G)
    • Altherr W., Linden A., and Heimgartner H., The 'azirine/oxazolone method' in peptaibol synthesis: preparation of a derivative of trichotoxin A-50 (G), Chemical & Biodiversity, 2007, 4, 1144-69.
    • (2007) Chemical & Biodiversity , vol.4 , pp. 1144-1169
    • Altherr, W.1    Linden, A.2    Heimgartner, H.3
  • 39
    • 79961162233 scopus 로고    scopus 로고
    • Site-selective incorporation of thioamidelinkages into a growing peptide via variation of the "azirine/oxazolone method"
    • (ECSOC-1), Sep
    • Lehmann J., Linden A., and Heimgartner H., Site-selective incorporation of thioamidelinkages into a growing peptide via variation of the "azirine/oxazolone method", International Electronic Conference on Synthetic Organic Chemistry (ECSOC-1), www.mdpi.org/ecsoc/, 1-30 Sep. 1997.
    • (1997) International Electronic Conference on Synthetic Organic Chemistry , pp. 1-30
    • Lehmann, J.1    Linden, A.2    Heimgartner, H.3
  • 40
    • 67749130969 scopus 로고    scopus 로고
    • Synthesis of a regular 24-membered cyclodepsipeptide by direct amide cyclization
    • Kottgen P., Linden A., and Heimgartner H., Synthesis of a regular 24-membered cyclodepsipeptide by direct amide cyclization, A Journal of Chemical Sciences, 2009, 64b, 689-698.
    • (2009) A Journal of Chemical Sciences , vol.64 b , pp. 689-698
    • Kottgen, P.1    Linden, A.2    Heimgartner, H.3
  • 41
    • 31344454289 scopus 로고    scopus 로고
    • The 'azirine/oxazolone method' on solid phase: Introduction of various α,α-disubstituted α- amino acids
    • Stamm S., Linden A., and Heimgartner H., The 'azirine/oxazolone method' on solid phase: introduction of various α,α-disubstituted α- amino acids, Helvetica Chimica Acta, 2006, 89, 1-15.
    • (2006) Helvetica Chimica Acta , vol.89 , pp. 1-15
    • Stamm, S.1    Linden, A.2    Heimgartner, H.3
  • 42
    • 0033368041 scopus 로고    scopus 로고
    • Asymmetric alcoholysis of 2-phenyl-5(4H)- oxazolones by the catalytic mixture of cyclo[(S)-His-(S)-Phe] with chiral auxiliaries
    • Xie L., Hua W., Chan A.S.C., and Leung Y.C., Asymmetric alcoholysis of 2-phenyl-5(4H)- oxazolones by the catalytic mixture of cyclo[(S)-His-(S)-Phe] with chiral auxiliaries, Tetrahedron: Asymmetry, 1999, 10, 4715-4728.
    • (1999) Tetrahedron: Asymmetry , vol.10 , pp. 4715-4728
    • Xie, L.1    Hua, W.2    Chan, A.S.C.3    Leung, Y.C.4
  • 43
    • 0029682693 scopus 로고    scopus 로고
    • Crystallisationinduced dynamic resolution of dipeptidederived 5(4H)-oxazolones
    • Stock H.T., and Turner N.J., Crystallisationinduced dynamic resolution of dipeptidederived 5(4H)-oxazolones, Tetrahedron Letters, 1996, 37, 6575-6578.
    • (1996) Tetrahedron Letters , vol.37 , pp. 6575-6578
    • Stock, H.T.1    Turner, N.J.2
  • 46
    • 79961152144 scopus 로고    scopus 로고
    • Oxazolinone derivatives, Process for preparing the same and use of the same, United States Patent, Patent No: US 5691278, Nov
    • Park et al, Oxazolinone derivatives, Process for preparing the same and use of the same, United States Patent, Patent No: US 5691278, Nov. 25, 1997.
    • (1997) , pp. 25
    • Park1
  • 47
    • 61649088179 scopus 로고    scopus 로고
    • A simple and efficient method for the synthesis of Erlenmeyer azlactones
    • Conway P.A., Devine K., and Paradisi F., A simple and efficient method for the synthesis of Erlenmeyer azlactones, Tetrahedron, 2009, 65, 2935-2938.
    • (2009) Tetrahedron , vol.65 , pp. 2935-2938
    • Conway, P.A.1    Devine, K.2    Paradisi, F.3
  • 48
    • 70349109541 scopus 로고    scopus 로고
    • Synthesis and biological activity of 4-(4- hydroxybenzylidene)-2-(substituted styryl) oxazol-5-ones and their o-glucosides
    • Taile V., Hatzade K., Gaidhane P., and Ingle V., Synthesis and biological activity of 4-(4- hydroxybenzylidene)-2-(substituted styryl) oxazol-5-ones and their o-glucosides, Turkish Journal of Chemistry, 2009, 33, 295-305.
    • (2009) Turkish Journal of Chemistry , vol.33 , pp. 295-305
    • Taile, V.1    Hatzade, K.2    Gaidhane, P.3    Ingle, V.4
  • 49
    • 1642544567 scopus 로고    scopus 로고
    • Fragmentation of deprotonated N-benzoylpeptides: Formation of deprotonated oxazolones
    • Harrison A.G., and Young A.B., Fragmentation of deprotonated N-benzoylpeptides: formation of deprotonated oxazolones, Journal of the American Society for Mass Spectrometry, 2004, 15, 446-456.
    • (2004) Journal of the American Society For Mass Spectrometry , vol.15 , pp. 446-456
    • Harrison, A.G.1    Young, A.B.2
  • 51
    • 79952744556 scopus 로고    scopus 로고
    • Oxazolone versus macrocycle structures for Leu-Enkephalin b2-b4: Insights from infrared multiple-photon dissociation spectroscopy and gas-phase hydrogen/deuterium exchange
    • Chen X., Steill J.D., Oomens J., and Polfer N.C., Oxazolone versus macrocycle structures for Leu-Enkephalin b2-b4: insights from infrared multiple-photon dissociation spectroscopy and gas-phase hydrogen/deuterium exchange, Journal of the American Society for Mass Spectrometry, 2010, 21, 1313-1321.
    • (2010) Journal of the American Society For Mass Spectrometry , vol.21 , pp. 1313-1321
    • Chen, X.1    Steill, J.D.2    Oomens, J.3    Polfer, N.C.4
  • 52
    • 48249148301 scopus 로고    scopus 로고
    • Synthesis and study of some compounds containing oxazolone ring showing biological activity
    • Tandel R.C., and Mammen D., Synthesis and study of some compounds containing oxazolone ring showing biological activity, Indian Journal of Chemistry, 2008, 47B, 932-937.
    • (2008) Indian Journal of Chemistry , vol.47 B , pp. 932-937
    • Tandel, R.C.1    Mammen, D.2
  • 54
    • 0036497367 scopus 로고    scopus 로고
    • Reaction of 4- benzylidene-2-methyl-5-oxazolone with amines, Part 2: Influence of substituents in para-position in the phenyl ring and a substituent on amine nitrogen atom on the reaction kinetics
    • Betlakowska B., Baneckl B., Czaplewski C., Lankiewicz C., and Wiczk W., Reaction of 4- benzylidene-2-methyl-5-oxazolone with amines, Part 2: influence of substituents in para-position in the phenyl ring and a substituent on amine nitrogen atom on the reaction kinetics, International Journal of Chemical Kinetics, 2002, 34, 148-155.
    • (2002) International Journal of Chemical Kinetics , vol.34 , pp. 148-155
    • Betlakowska, B.1    Baneckl, B.2    Czaplewski, C.3    Lankiewicz, C.4    Wiczk, W.5
  • 55
    • 0037013823 scopus 로고    scopus 로고
    • Reactivity of (Z)-4-arylidene- 5(4H)-oxazolones: [4+2] cycloaddition versus [4+3] cycloaddition/nucleophilic trapping
    • Avenoza A., Busto J.H., Cativiela C., and Peregrina J.M., Reactivity of (Z)-4-arylidene- 5(4H)-oxazolones: [4+2] cycloaddition versus [4+3] cycloaddition/nucleophilic trapping, Tetrahedron Letters, 2002, 43, 4167-4170.
    • (2002) Tetrahedron Letters , vol.43 , pp. 4167-4170
    • Avenoza, A.1    Busto, J.H.2    Cativiela, C.3    Peregrina, J.M.4
  • 56
    • 79961157768 scopus 로고
    • A Michael addition approach towards a thienamycin synthesis, Open Access Dissertations and Theses, 1983
    • Paper
    • Leod M., Allan R., A Michael addition approach towards a thienamycin synthesis, Open Access Dissertations and Theses, 1983, Paper 1397, pp. 1-249.
    • (1397) , pp. 1-249
    • Leod, M.1    Allan, R.2
  • 57
    • 2842598833 scopus 로고
    • Thermolysis of derivatives of ß-substituted α-(1-tetrazollyl) acrylic acids I. Formation of some imidazolones and a thiazolone
    • Lykkeberg J., and Klitgaard N.A., Thermolysis of derivatives of ß-substituted α-(1-tetrazollyl) acrylic acids I. Formation of some imidazolones and a thiazolone, Acta Chemica Scandinavica, 1972, 26, 2687-2694.
    • (1972) Acta Chemica Scandinavica , vol.26 , pp. 2687-2694
    • Lykkeberg, J.1    Klitgaard, N.A.2
  • 58
    • 0037053905 scopus 로고    scopus 로고
    • Synthesis of polyconjugated carbazolyl-oxazolones by a tandem hydrozirconation-Erlenmeyer reaction. Study of their hyperpolarizability values
    • Diaz J.L., Villacampa B., Calahorraa F.L., and Velasco D., Synthesis of polyconjugated carbazolyl-oxazolones by a tandem hydrozirconation-Erlenmeyer reaction. Study of their hyperpolarizability values, Tetrahedron Letters, 2002, 43, 4333-4337.
    • (2002) Tetrahedron Letters , vol.43 , pp. 4333-4337
    • Diaz, J.L.1    Villacampa, B.2    Calahorraa, F.L.3    Velasco, D.4
  • 59
    • 22144497816 scopus 로고    scopus 로고
    • Solid-phase synthesis of oxazolones and other heterocycles via Wang resin-bound diazocarbonyls
    • Yamashita M., Lee S.H., Koch G., Zimmermann J., Clapham B., and Janda K.D., Solid-phase synthesis of oxazolones and other heterocycles via Wang resin-bound diazocarbonyls, Tetrahedron Letters, 2005, 46, 5495-5498.
    • (2005) Tetrahedron Letters , vol.46 , pp. 5495-5498
    • Yamashita, M.1    Lee, S.H.2    Koch, G.3    Zimmermann, J.4    Clapham, B.5    Janda, K.D.6
  • 60
    • 1642619403 scopus 로고    scopus 로고
    • Potent and selective inhibitors of bacterial methionyl tRNA synthetase derived from an oxazolone- dipeptide scaffold
    • Tandon M., Coffen D.L., Gallant P., Keith D., and Ashwell M.A., Potent and selective inhibitors of bacterial methionyl tRNA synthetase derived from an oxazolone- dipeptide scaffold, Bioorganic & Medicinal Chemistry Letters, 2004, 14, 1909-1911.
    • (2004) Bioorganic & Medicinal Chemistry Letters , vol.14 , pp. 1909-1911
    • Tandon, M.1    Coffen, D.L.2    Gallant, P.3    Keith, D.4    Ashwell, M.A.5
  • 61
    • 0642309875 scopus 로고    scopus 로고
    • Synthesis and biological activity of novel 5-(ω- aryloxyalkyl)oxazole derivatives as brainderived neurotrophic factor inducers
    • Maekawa T., Sakai N., Tawada H., Murase K., Hazama M., Sugiyama Y., and Momose Y., Synthesis and biological activity of novel 5-(ω- aryloxyalkyl)oxazole derivatives as brainderived neurotrophic factor inducers, Chemical and Pharmaceutical Bulletin, 2003, 51, 565-573.
    • (2003) Chemical and Pharmaceutical Bulletin , vol.51 , pp. 565-573
    • Maekawa, T.1    Sakai, N.2    Tawada, H.3    Murase, K.4    Hazama, M.5    Sugiyama, Y.6    Momose, Y.7
  • 63
    • 0021023338 scopus 로고
    • o-Hydroxyphenylureas. Intermediates in the urea fusion synthesis of 2- benzoxazolinones
    • Nachman R.J., o-Hydroxyphenylureas. Intermediates in the urea fusion synthesis of 2- benzoxazolinones, Journal of Heterocyclic Chemistry, 1983, 20, 1423-1425.
    • (1983) Journal of Heterocyclic Chemistry , vol.20 , pp. 1423-1425
    • Nachman, R.J.1
  • 64
    • 0020397066 scopus 로고
    • Convenient Preparation of 2- Benzoxazolinones with 1,1- Carbonyldiimidazole
    • Nachman R.J., Convenient Preparation of 2- Benzoxazolinones with 1,1- Carbonyldiimidazole, Journal of Heterocyclic Chemistry, 1982, 19, 1545-1547.
    • (1982) Journal of Heterocyclic Chemistry , vol.19 , pp. 1545-1547
    • Nachman, R.J.1
  • 65
    • 40849085595 scopus 로고    scopus 로고
    • An efficient and eco-friendly process for the conversion of carbon dioxide into oxazolones and oxazolidinones under supercritical conditions
    • Jiang H., Zhao J., and Wang A., an efficient and eco-friendly process for the conversion of carbon dioxide into oxazolones and oxazolidinones under supercritical conditions, Journal of Synthetic Organic Chemistry, 2008, 39, 763-769.
    • (2008) Journal of Synthetic Organic Chemistry , vol.39 , pp. 763-769
    • Jiang, H.1    Zhao, J.2    Wang, A.3
  • 66
    • 34247239467 scopus 로고    scopus 로고
    • Nickel(II)-catalysed oxidative guanine and DNA damage beyond 8- oxoguanine
    • Kelly, M. C., Whitaker, G., White, B., and Smyth, M. R., Nickel(II)-catalysed oxidative guanine and DNA damage beyond 8- oxoguanine, Free radical biology & medicine, 2007, 42, 1680-1689.
    • (2007) Free Radical Biology & Medicine , vol.42 , pp. 1680-1689
    • Kelly, M.C.1    Whitaker, G.2    White, B.3    Smyth, M.R.4
  • 67
    • 72149092940 scopus 로고    scopus 로고
    • One-pot process to Z-α-benzoylaminoacrylic acid methyl esters via potassium phosphate-catalyzed Erlenmeyer reaction
    • Cleary T., Brice J., Kennedy N., and Chavez, F., One-pot process to Z-α-benzoylaminoacrylic acid methyl esters via potassium phosphate-catalyzed Erlenmeyer reaction, Tetrahedron Letters, 2010, 51, 625-628.
    • (2010) Tetrahedron Letters , vol.51 , pp. 625-628
    • Cleary, T.1    Brice, J.2    Kennedy, N.3    Chavez, F.4
  • 68
    • 0031550878 scopus 로고    scopus 로고
    • Synthetic studies on threonines. The preparation of protected derivatives of D-allo- and L-allo-Threonine for peptide synthesis
    • Williams P.L., Sanchez A., Carulla N., Ochoa T., and Giralt E., Synthetic studies on threonines. The preparation of protected derivatives of D-allo- and L-allo-Threonine for peptide synthesis, Tetrahedron, 1997, 53, 3369-3382.
    • (1997) Tetrahedron , vol.53 , pp. 3369-3382
    • Williams, P.L.1    Sanchez, A.2    Carulla, N.3    Ochoa, T.4    Giralt, E.5
  • 69
    • 0035212685 scopus 로고    scopus 로고
    • Development of a stereoselective practical synthetic route to Indolmycin, a candidate Anti-H. pylori agent
    • Hasuoka A., Nakayama Y., Adachi M., Kamiguchi H., and Kamiyama K., Development of a stereoselective practical synthetic route to Indolmycin, a candidate Anti-H. pylori agent, Chemical and Pharmaceutical Bulletin, 2001, 49, 1604-1608.
    • (2001) Chemical and Pharmaceutical Bulletin , vol.49 , pp. 1604-1608
    • Hasuoka, A.1    Nakayama, Y.2    Adachi, M.3    Kamiguchi, H.4    Kamiyama, K.5
  • 71
    • 0000103910 scopus 로고
    • 2-Alkoxy- S(4H)-oxazolones from N-alkoxy carbonylamino acids and their implication in carbodiimide-mediated reactions in peptide synthesis
    • Benoiton N.L., and Chen F.M.F., 2-Alkoxy- S(4H)-oxazolones from N-alkoxy carbonylamino acids and their implication in carbodiimide-mediated reactions in peptide synthesis, Canadian Journal of Chemistry, 1981, 59, 384-389.
    • (1981) Canadian Journal of Chemistry , vol.59 , pp. 384-389
    • Benoiton, N.L.1    Chen, F.M.F.2
  • 72
    • 0032510422 scopus 로고    scopus 로고
    • Synthesis of 4-carboethoxy-4-oxazolin-2-ones from 3-nosyloxy-2-ketoesters
    • Hoffman R.V., Johnson M.C., and Okonya J.F., Synthesis of 4-carboethoxy-4-oxazolin-2-ones from 3-nosyloxy-2-ketoesters, Tetrahedron Letters, 1998, 39, 1283-1286.
    • (1998) Tetrahedron Letters , vol.39 , pp. 1283-1286
    • Hoffman, R.V.1    Johnson, M.C.2    Okonya, J.F.3


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