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Volumn 8, Issue 11, 2010, Pages 2755-2780

Thiazole and oxazole alkaloids: Isolation and synthesis

Author keywords

Marine; Oxazole; Thiazole

Indexed keywords

AERUCYCLAMIDE A; AERUCYCLAMIDE B; AERUCYCLAMIDE C; AERUCYCLAMIDE D; ALKALOID; APRATOXIN A; ARIAKEMICINS A; ARIAKEMICINS B; BACILLAMIDE A; BACILLAMIDE B; BACILLAMIDE C; BISEBROMOAMIDE; GRASSYPEPTOLIDE; HEXAMOLLAMIDE; HOIAMIDE A; LARGAZOLE; MICROCYCLAMIDE DERIVATIVE; MOLLAMIDE B; MOLLAMIDE C; NEOBACILLAMIDE A; NEODYSIDENIN; NEOPELTOLIDE; OXAZOLE; PETALLAMIDE A; SCLERITODERMIN A; THIAZOLE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG; URUKTHAPELSTATIN A; VENTURAMIDE A; VENTURAMIDE B;

EID: 78649756003     PISSN: None     EISSN: 16603397     Source Type: Journal    
DOI: 10.3390/md8112755     Document Type: Review
Times cited : (178)

References (87)
  • 1
    • 37249089097 scopus 로고    scopus 로고
    • Bacillamides from a hypersaline microbial mat bacterium
    • Aaron, M.S.; Richard, A.L.; David, C.R. Bacillamides from a hypersaline microbial mat bacterium. J. Nat. Prod. 2007, 70, 1793-1795.
    • (2007) J. Nat. Prod. , vol.70 , pp. 1793-1795
    • Aaron, M.S.1    Richard, A.L.2    David, C.R.3
  • 2
    • 65749086659 scopus 로고    scopus 로고
    • Neoobacillamide A, a novel thiazole-containing alkaloid from the marine bacterium bacillus vallismortis C89, associated with south china sea sponge Dysidea avara
    • Yu, L.; Li, Z.; Peng, C.; Li, Z.; Guo, Y. Neoobacillamide A, a novel thiazole-containing alkaloid from the marine bacterium bacillus vallismortis C89, associated with south china sea sponge Dysidea avara. Helv. Chim. 2009, 92, 607-612.
    • (2009) Helv. Chim. , vol.92 , pp. 607-612
    • Yu, L.1    Li, Z.2    Peng, C.3    Li, Z.4    Guo, Y.5
  • 3
    • 34547223063 scopus 로고    scopus 로고
    • Urukthapelstatin A, a novel cytotoxic substance from marine-derived Mechercharimyces asporophorigenens YM11-542
    • Matsuo, Y.; Kanoh, K.; Imagawa, H.; Adachi, K.; Nishizawa, M.; Shizuri, Y. Urukthapelstatin A, a novel cytotoxic substance from marine-derived Mechercharimyces asporophorigenens YM11-542. J. Antib. 2007, 60, 256-260.
    • (2007) J. Antib. , vol.60 , pp. 256-260
    • Matsuo, Y.1    Kanoh, K.2    Imagawa, H.3    Adachi, K.4    Nishizawa, M.5    Shizuri, Y.6
  • 4
    • 34247109540 scopus 로고    scopus 로고
    • Venturamides a and B: Antimalarial constituents of the Panamanian marine cyanobacterium Oscillatoria sp
    • DOI 10.1021/np0605790
    • Linington, R.G.; González, J.; Ureña, L.; Romero, L.I.; Ortega-Barría, E.; Gerwick, W.H. Venturamides A and B: antimalarial constituents of the panamanian marine cyanobacterium Oscillatoria sp. J. Nat. Prod. 2007, 70, 397-401. (Pubitemid 46595746)
    • (2007) Journal of Natural Products , vol.70 , Issue.3 , pp. 397-401
    • Linington, R.G.1    Gonzalez, J.2    Urena, L.-D.3    Romero, L.I.4    Ortega-Barria, E.5    Gerwick, W.H.6
  • 5
    • 49049085673 scopus 로고    scopus 로고
    • Aerucyclamides A and B: Isolation and synthesis of toxic ribosomal heterocyclic peptides from the cyanobacterium Microcystis aeruginosa PCC 7806
    • Portmann, C.; Blom, J.F.; Gademann, K.; Jüttner, F. Aerucyclamides A and B: isolation and synthesis of toxic ribosomal heterocyclic peptides from the cyanobacterium Microcystis aeruginosa PCC 7806. J. Nat. Prod. 2008, 71, 1193-1196.
    • (2008) J. Nat. Prod. , vol.71 , pp. 1193-1196
    • Portmann, C.1    Blom, J.F.2    Gademann, K.3    Jüttner, F.4
  • 6
    • 58149161845 scopus 로고    scopus 로고
    • Isolation of Aerucyclamides C and D and structure revision of Microcyclamide 7806A: Heterocyclic ribosomal peptides from Microcystis aeruginosa PCC 7806 and their antiparasite evaluation
    • Portmann, C.; Blom, J.F.; Kaiser, M.; Brun, R.; Jüttner, F.; Gademann, K. Isolation of Aerucyclamides C and D and structure revision of Microcyclamide 7806A: heterocyclic ribosomal peptides from Microcystis aeruginosa PCC 7806 and their antiparasite evaluation. J. Nat. Prod. 2008, 71, 1891-1896.
    • (2008) . J. Nat. Prod. , vol.71 , pp. 1891-1896
    • Portmann, C.1    Blom, J.F.2    Kaiser, M.3    Brun, R.4    Jüttner, F.5    Gademann, K.6
  • 7
    • 47549088623 scopus 로고    scopus 로고
    • Hexamollamide, a hexapeptide from an Okinawan ascidian Didemnum molle
    • Teruya, T.; Sasaki, H.; Suenaga, K. Hexamollamide, a hexapeptide from an Okinawan ascidian Didemnum molle. Tetraedron Lett. 2008, 49, 5297-5299.
    • (2008) Tetraedron Lett. , vol.49 , pp. 5297-5299
    • Teruya, T.1    Sasaki, H.2    Suenaga, K.3
  • 9
    • 0000192163 scopus 로고    scopus 로고
    • Patellins 1-6 and trunkamide A: Novel cyclic hexa-, hepta- and octa-peptides from colonial ascidians, Lissoclinum sp
    • Carroll, A.R.; Coll, J.C.; Bourne, D.J.; MacLeod, J.K.; Ireland, C.M.; Bowden, B.F. Patellins 1-6 and trunkamide A: novel cyclic hexa-, hepta- and octa-peptides from colonial ascidians, Lissoclinum sp. Aust. J. Chem. 1996, 49, 659-667.
    • (1996) Aust. J. Chem. , vol.49 , pp. 659-667
    • Carroll, A.R.1    Coll, J.C.2    Bourne, D.J.3    MacLeod, J.K.4    Ireland, C.M.5    Bowden, B.F.6
  • 11
    • 39049135494 scopus 로고    scopus 로고
    • Structure and activity of largazole, a potent antiproliferative agent from the floridian marine cyanobacterium Symploca sp
    • Taori, K.; Paul, V.J.; Luesch, H. Structure and activity of largazole, a potent antiproliferative agent from the floridian marine cyanobacterium Symploca sp. J. Am. Chem. Soc. 2008, 130, 1806-1807.
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 1806-1807
    • Taori, K.1    Paul, V.J.2    Luesch, H.3
  • 12
    • 69049091880 scopus 로고    scopus 로고
    • Hoiamide A, a sodium channel activator of unusual architecture from a consortium of two papua new guinea cyanobacteria
    • Pereira, A.; Cao, Z.; Murray, T.F.; Gerwick, W.H. Hoiamide A, a sodium channel activator of unusual architecture from a consortium of two papua new guinea cyanobacteria. Chem. Biol. 2009, 16, 893-906.
    • (2009) Chem. Biol. , vol.16 , pp. 893-906
    • Pereira, A.1    Cao, Z.2    Murray, T.F.3    Gerwick, W.H.4
  • 13
    • 72049111734 scopus 로고    scopus 로고
    • Hoiamide A, a sodium channel activator of unusual architecture from a consortium of two papua new guinea cyanobacteria
    • Pereira, A.; Cao, Z.; Murray, T.F.; Gerwick, W.H. Hoiamide A, a sodium channel activator of unusual architecture from a consortium of two papua new guinea cyanobacteria. Chem. Biol. 2009, 16, 1208.
    • (2009) Chem. Biol. , vol.16 , pp. 1208
    • Pereira, A.1    Cao, Z.2    Murray, T.F.3    Gerwick, W.H.4
  • 14
    • 77649184195 scopus 로고    scopus 로고
    • Novel thiazole and oxazole containing cyclic hexapeptides from a waterbloom of the cyanobacterium Microcystis sp
    • Raveh, A.; Moshe, S.; Evron, Z.; Flescher, E.; Carmeli, S. Novel thiazole and oxazole containing cyclic hexapeptides from a waterbloom of the cyanobacterium Microcystis sp. Tetrahedron 2010, 66, 2705-2712.
    • (2010) Tetrahedron , vol.66 , pp. 2705-2712
    • Raveh, A.1    Moshe, S.2    Evron, Z.3    Flescher, E.4    Carmeli, S.5
  • 15
    • 43549124620 scopus 로고    scopus 로고
    • Total structure determination of grassypeptolide, a new marine cyanobacterial cytotoxin
    • Kwan, J.; Rocca J.R.; Abboud, K.A.; Paul, V.J.; Luesch, H. Total structure determination of grassypeptolide , a new marine cyanobacterial cytotoxin. Org. Lett. 2008, 10, 789-792.
    • (2008) Org. Lett. , vol.10 , pp. 789-792
    • Kwan, J.1    Rocca, J.R.2    Abboud, K.A.3    Paul, V.J.4    Luesch, H.5
  • 16
    • 70350637641 scopus 로고    scopus 로고
    • Bisebromoamide, a potent cytotoxic peptide from the marine cyanobacterium Lyngbya sp. Isolation, stereostructure, and biological activity
    • Teruya, T.; Sasaki, H.; Fukazawa, H.; Suenaga, K. Bisebromoamide, a potent cytotoxic peptide from the marine cyanobacterium Lyngbya sp. Isolation, stereostructure, and biological activity. Org. Lett. 2009, 11, 5062-5065.
    • (2009) Org. Lett. , vol.11 , pp. 5062-5065
    • Teruya, T.1    Sasaki, H.2    Fukazawa, H.3    Suenaga, K.4
  • 17
    • 33846839284 scopus 로고    scopus 로고
    • Toward the total synthesis of scleritodermin A: Preparation of the C1-N15 fragment
    • Sellanes, D.; Manta, E.; Serra, G. Toward the total synthesis of scleritodermin A: preparation of the C1-N15 fragment. Tetrahedron Lett. 2007, 48, 1827-1830.
    • (2007) Tetrahedron Lett. , vol.48 , pp. 1827-1830
    • Sellanes, D.1    Manta, E.2    Serra, G.3
  • 18
    • 55949131228 scopus 로고    scopus 로고
    • Total synthesis of the originally proposed and revised structures of scleritodermin A
    • Liu, S.; Cui, Y.-M.; Nan, F.-J. Total synthesis of the originally proposed and revised structures of scleritodermin A. Org. Lett. 2008, 10, 3765-3768.
    • (2008) Org. Lett. , vol.10 , pp. 3765-3768
    • Liu, S.1    Cui, Y.-M.2    Nan, F.-J.3
  • 20
    • 58149154420 scopus 로고    scopus 로고
    • A new total synthesis of patellamide A
    • Garcia-Reynaga, P.; VanNieuwenhze, M.S. A new total synthesis of patellamide A. Org. Lett. 2008, 10, 4621-4623.
    • (2008) Org. Lett. , vol.10 , pp. 4621-4623
    • Garcia-Reynaga, P.1    VanNieuwenhze, M.S.2
  • 21
    • 46049100010 scopus 로고    scopus 로고
    • Total Synthesis and Molecular Target of Largazole, a Histone Deacetylase Inhibitor
    • Ying, Y.; Taori, K.; Kim, H.; Hong, J.; Luesch, H. Total Synthesis and Molecular Target of Largazole , a Histone Deacetylase Inhibitor. J. Am. Chem. Soc. 2008, 130, 8455-8459.
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 8455-8459
    • Ying, Y.1    Taori, K.2    Kim, H.3    Hong, J.4    Luesch, H.5
  • 22
    • 54049152858 scopus 로고    scopus 로고
    • A Concise Total Synthesis of Largazole, Solution Structure, and Some Preliminary Structure Activity Relationships
    • Nasveschuk, C.G.; Ungermannova, D.; Liu, X.; Phillips, A.J. A Concise Total Synthesis of Largazole , Solution Structure, and Some Preliminary Structure Activity Relationships. Org. Lett. 2008, 10, 3595-3598.
    • (2008) Org. Lett. , vol.10 , pp. 3595-3598
    • Nasveschuk, C.G.1    Ungermannova, D.2    Liu, X.3    Phillips, A.J.4
  • 23
    • 52049119362 scopus 로고    scopus 로고
    • Synthesis and biological activity of largazole and derivatives
    • Seiser, T.; Kamena, F.; Cramer, N. Synthesis and biological activity of largazole and derivatives. Angew. Chem. Int. Ed. 2008, 47, 6483-6485.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 6483-6485
    • Seiser, T.1    Kamena, F.2    Cramer, N.3
  • 24
    • 50249144006 scopus 로고    scopus 로고
    • Total synthesis and biological mode of action of largazole: A potent class I histone deacetylase inhibitor
    • Bowers, A.; West, N.; Taunton, J.; Schreiber, S.L.; Bradner, J.E.; Williams, R.M. Total synthesis and biological mode of action of largazole: A potent class I histone deacetylase inhibitor. J. Am. Chem. Soc. 2008, 130, 11219-11222.
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 11219-11222
    • Bowers, A.1    West, N.2    Taunton, J.3    Schreiber, S.L.4    Bradner, J.E.5    Williams, R.M.6
  • 25
    • 55949099039 scopus 로고    scopus 로고
    • Enantioselective total synthesis of (+)-largazole, a potent inhibitor of histone deacetylase
    • Ghosh, A.K.; Kulkarni, S. Enantioselective total synthesis of (+)-largazole, a potent inhibitor of histone deacetylase. Org. Lett. 2008, 10, 3907-3909.
    • (2008) Org. Lett. , vol.10 , pp. 3907-3909
    • Ghosh, A.K.1    Kulkarni, S.2
  • 26
    • 55949094932 scopus 로고    scopus 로고
    • Synthesis and activity of largazole analogues with linker and macrocycle modification
    • Ying, Y.; Liu, Y.; Byeon, S.R.; Kim, H.; Luesch, H.; Hong, J. Synthesis and activity of largazole analogues with linker and macrocycle modification. Org. Lett. 2008, 10, 4021-4024.
    • (2008) Org. Lett. , vol.10 , pp. 4021-4024
    • Ying, Y.1    Liu, Y.2    Byeon, S.R.3    Kim, H.4    Luesch, H.5    Hong, J.6
  • 28
    • 54149114729 scopus 로고    scopus 로고
    • Total synthesis of largazole and its biological evaluation
    • Numajiri, Y.; Takahashi, T.; Takagi, M.; Shin-ya, K.; Doi, T. Total synthesis of largazole and its biological evaluation. Synlett 2008, 2483-2486.
    • (2008) Synlett , pp. 2483-2486
    • Numajiri, Y.1    Takahashi, T.2    Takagi, M.3    Shin-ya, K.4    Doi, T.5
  • 30
    • 64049106355 scopus 로고    scopus 로고
    • Synthesis and histone deacetylase inhibitory activity of largazole analogs: Alteration of the zinc-binding domain and macrocyclic scaffold
    • Bowers, A.A.; West, N.; Newkirk, T.L.; Troutman-Youngman, A.E.; Schreiber, S.L.; Wiest, O.; Bradner, J.E.; Williams, R.M. Synthesis and histone deacetylase inhibitory activity of largazole analogs: alteration of the zinc-binding domain and macrocyclic scaffold. Org. Lett. 2009, 11, 1301-1304.
    • (2009) Org. Lett. , vol.11 , pp. 1301-1304
    • Bowers, A.A.1    West, N.2    Newkirk, T.L.3    Troutman-Youngman, A.E.4    Schreiber, S.L.5    Wiest, O.6    Bradner, J.E.7    Williams, R.M.8
  • 31
    • 62349125284 scopus 로고    scopus 로고
    • Syntheses and biological activity of the HDAC class I inhibitor largazole
    • Seiser, T.; Cramer, N. Syntheses and biological activity of the HDAC class I inhibitor largazole. Chimia 2009, 63, 19-22.
    • (2009) Chimia , vol.63 , pp. 19-22
    • Seiser, T.1    Cramer, N.2
  • 32
    • 68149161259 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of C7-demethyl largazole analogues
    • Chen, F.; Gao, A.-H.; Li, J.; Nan, F.-J. Synthesis and biological evaluation of C7-demethyl largazole analogues. ChemMedChem 2009, 4, 1269-1272.
    • (2009) ChemMedChem , vol.4 , pp. 1269-1272
    • Chen, F.1    Gao, A.-H.2    Li, J.3    Nan, F.-J.4
  • 33
    • 70349209217 scopus 로고    scopus 로고
    • Total synthesis of (+)-largazole, a histone deacetylase inhibitor
    • Yan, W.; O'Doherty, G.A. Total synthesis of (+)-largazole, a histone deacetylase inhibitor. Chemtracts 2009, 22, 50-58.
    • (2009) Chemtracts , vol.22 , pp. 50-58
    • Yan, W.1    O'Doherty, G.A.2
  • 34
    • 70449396598 scopus 로고    scopus 로고
    • Total synthesis of largazole-devolution of a novel synthetic strategy
    • Wang, B.; Forsyth, C.J. Total synthesis of largazole-devolution of a novel synthetic strategy. Syntesis 2009, 2873-2880.
    • (2009) Syntesis , pp. 2873-2880
    • Wang, B.1    Forsyth, C.J.2
  • 35
    • 77949831890 scopus 로고    scopus 로고
    • Total synthesis and biological evaluation of largazole and derivatives with promising selectivity for cancers cells
    • Zeng, X.; Yin, B.; Hu, Z.; Liao, C.; Liu, J.; Li, S.; Li, Z.; Nicklaus, M.C.; Zhou, G.; Jiang, S. Total synthesis and biological evaluation of largazole and derivatives with promising selectivity for cancers cells. Org. Lett. 2010, 12, 1368-1371.
    • (2010) Org. Lett. , vol.12 , pp. 1368-1371
    • Zeng, X.1    Yin, B.2    Hu, Z.3    Liao, C.4    Liu, J.5    Li, S.6    Li, Z.7    Nicklaus, M.C.8    Zhou, G.9    Jiang, S.10
  • 36
    • 77953740289 scopus 로고    scopus 로고
    • Synthesis and biological characterization of the histone deacetylase inhibitor largazole and C7-modified analogues
    • Souto, J.A.; Vaz, E.; Lepore, I.; Poppler, A.-C.; Franci, G.; Alvarez, R.; Altucci, L.; de Lera, A.R. Synthesis and biological characterization of the histone deacetylase inhibitor largazole and C7-modified analogues. J. Med. Chem. 2010, 53, 4654-4667.
    • (2010) J. Med. Chem. , vol.53 , pp. 4654-4667
    • Souto, J.A.1    Vaz, E.2    Lepore, I.3    Poppler, A.-C.4    Franci, G.5    Alvarez, R.6    Altucci, L.7    De Lera, A.R.8
  • 39
    • 76149091180 scopus 로고    scopus 로고
    • Valence tautomerism in titanium enolates: Catalytic radical haloalkylation and application in the total synthesis of neodysidenin
    • Beaumont, S.; Ilardi, E.A.; Monroe, L.R.; Zakarian, A. Valence tautomerism in titanium enolates: catalytic radical haloalkylation and application in the total synthesis of neodysidenin. J. Am. Chem. Soc. 2010, 132, 1482-1483.
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 1482-1483
    • Beaumont, S.1    Ilardi, E.A.2    Monroe, L.R.3    Zakarian, A.4
  • 40
    • 58149178729 scopus 로고    scopus 로고
    • Total synthesis of (-)-apratoxin A, 34-epimer, and its oxazoline analogue
    • Numajiri, Y.; Takahashi, T.; Doi, T. Total synthesis of (-)-apratoxin A, 34-epimer, and its oxazoline analogue. Chem. Asian J. 2009, 4, 111-125.
    • (2009) Chem. Asian J. , vol.4 , pp. 111-125
    • Numajiri, Y.1    Takahashi, T.2    Doi, T.3
  • 41
    • 77954119216 scopus 로고    scopus 로고
    • Total synthesis and stereochemical reassignment of bisebromoamide
    • Gao, X.; Liu, Y.; Kwong, S.; Xu, Z.; Ye, T. Total synthesis and stereochemical reassignment of bisebromoamide. Org. Lett. 2010, 12, 3018-3021.
    • (2010) Org. Lett. , vol.12 , pp. 3018-3021
    • Gao, X.1    Liu, Y.2    Kwong, S.3    Xu, Z.4    Ye, T.5
  • 43
    • 48849112548 scopus 로고    scopus 로고
    • Ariakemicins A and B, novel polyketide-peptide Antibiotics from a marine gliding bacterium of the genus Rapidithrix
    • Oku, N.; Adachi, K.; Matsuda, S.; Kasai, H.; Takatsuki, A.; Shizuri, Y. Ariakemicins A and B, novel polyketide-peptide Antibiotics from a marine gliding bacterium of the genus Rapidithrix. Org. Lett. 2008, 10, 2481-2484.
    • (2008) Org. Lett. , vol.10 , pp. 2481-2484
    • Oku, N.1    Adachi, K.2    Matsuda, S.3    Kasai, H.4    Takatsuki, A.5    Shizuri, Y.6
  • 45
    • 55449094954 scopus 로고    scopus 로고
    • Taumycins A and B, Two Bioactive Lipodepsipeptides from the Madagascar Sponge Fascaplysinopsis sp
    • Bishara, A.; Rudi, A.; Aknin, M.; Neumann, D.; Ben-Califa, N.; Kashman, Y. Taumycins A and B, Two Bioactive Lipodepsipeptides from the Madagascar Sponge Fascaplysinopsis sp. Org. Lett. 2008, 10, 4307-4309.
    • (2008) Org. Lett. , vol.10 , pp. 4307-4309
    • Bishara, A.1    Rudi, A.2    Aknin, M.3    Neumann, D.4    Ben-Califa, N.5    Kashman, Y.6
  • 48
    • 65649095546 scopus 로고    scopus 로고
    • Structure elucidation at the nanomole scale. 1. Trisoxazole macrolides and thiazole-containing cyclic peptides from the nudibranch Hexabranchus sanguineus
    • Dalisay, D.S.; Rogers, E.W.; Edison, A.S.; Molinski, T.F. Structure elucidation at the nanomole scale. 1. Trisoxazole macrolides and thiazole-containing cyclic peptides from the nudibranch Hexabranchus sanguineus. J. Nat. Prod. 2009, 72, 732-738.
    • (2009) J. Nat. Prod. , vol.72 , pp. 732-738
    • Dalisay, D.S.1    Rogers, E.W.2    Edison, A.S.3    Molinski, T.F.4
  • 50
    • 77955048478 scopus 로고    scopus 로고
    • Isolation, Structural Elucidation, and Absolute Stereochemistry of Enigmazole A, a Cytotoxic Phosphomacrolide from the Papua New Guinea Marine Sponge Cinachyrella enigmatica
    • Oku, N.; Takada, K.; Fuller, R.W.; Wilson, J.A.; Peach, M.L.; Pannell, L.K.; McMahon, J.B.; Gustafson, K.R. Isolation, Structural Elucidation, and Absolute Stereochemistry of Enigmazole A, a Cytotoxic Phosphomacrolide from the Papua New Guinea Marine Sponge Cinachyrella enigmatica. J. Am. Chem. Soc. 2010, 132, 10278-10285.
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 10278-10285
    • Oku, N.1    Takada, K.2    Fuller, R.W.3    Wilson, J.A.4    Peach, M.L.5    Pannell, L.K.6    McMahon, J.B.7    Gustafson, K.R.8
  • 52
    • 38349186964 scopus 로고    scopus 로고
    • Total Synthesis and Structural Revision of the Marine Macrolide Neopeltolide
    • Custar, D.W.; Zabawa, T.P.; Scheidt, K.A. Total Synthesis and Structural Revision of the Marine Macrolide Neopeltolide. J. Am. Chem. Soc. 2008, 130, 804-805.
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 804-805
    • Custar, D.W.1    Zabawa, T.P.2    Scheidt, K.A.3
  • 53
    • 69449102915 scopus 로고    scopus 로고
    • Total synthesis and structure-activity investigation of the marine natural product neopeltolide
    • Custar, D.W.; Zabawa, T.P.; Hines, J.; Crews, C.M.; Scheidt, K.A. Total synthesis and structure-activity investigation of the marine natural product neopeltolide. J. Am. Chem. Soc. 2009, 131, 12406-12414.
    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 12406-12414
    • Custar, D.W.1    Zabawa, T.P.2    Hines, J.3    Crews, C.M.4    Scheidt, K.A.5
  • 54
    • 45549090228 scopus 로고    scopus 로고
    • Total synthesis of (+)-neopeltolide by a Prins macrocyclization
    • Woo, S.K.; Kwon, M.S.; Lee, E. Total synthesis of (+)-neopeltolide by a Prins macrocyclization. Angew. Chem. Int. Ed. 2008, 47, 3242-3244.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 3242-3244
    • Woo, S.K.1    Kwon, M.S.2    Lee, E.3
  • 56
    • 54749110587 scopus 로고    scopus 로고
    • Total synthesis of the marine macrolide (+)-neopeltolide
    • Paterson, I.; Miller, N.A. Total synthesis of the marine macrolide (+)-neopeltolide. Chem. Comm. 2008, 39, 4708-4710.
    • (2008) Chem. Comm. , vol.39 , pp. 4708-4710
    • Paterson, I.1    Miller, N.A.2
  • 57
    • 57149124789 scopus 로고    scopus 로고
    • Total synthesis and biological activity of neopeltolide and analogues
    • Vintonyak, V.V.; Kunze, B.; Sasse, F.; Maier, M.E. Total synthesis and biological activity of neopeltolide and analogues. Chem. Eur. J. 2008, 14, 11132-11140.
    • (2008) Chem. Eur. J. , vol.14 , pp. 11132-11140
    • Vintonyak, V.V.1    Kunze, B.2    Sasse, F.3    Maier, M.E.4
  • 58
    • 58149164909 scopus 로고    scopus 로고
    • Concise Enantioselective Total Synthesis of Neopeltolide Macrolactone Highlighted by Ether Transfer
    • Kartika, R.; Gruffi, T.R.; Taylor, R.E. Concise Enantioselective Total Synthesis of Neopeltolide Macrolactone Highlighted by Ether Transfer. Org. Lett. 2008, 10, 5047-5050.
    • (2008) Org. Lett. , vol.10 , pp. 5047-5050
    • Kartika, R.1    Gruffi, T.R.2    Taylor, R.E.3
  • 59
    • 78649746530 scopus 로고    scopus 로고
    • Total synthesis of (+)-neopeltolide, antitumor marine macrolide
    • Sasaki, M.; Fuwa, H. Total synthesis of (+)-neopeltolide, antitumor marine macrolide. Farumashia 2009, 45, 439-443.
    • (2009) Farumashia , vol.45 , pp. 439-443
    • Sasaki, M.1    Fuwa, H.2
  • 60
    • 70349902444 scopus 로고    scopus 로고
    • Total Synthesis of the Antiproliferative Macrolide (+)-Neopeltolide
    • Guinchard, X.; Roulland, E. Total Synthesis of the Antiproliferative Macrolide (+)-Neopeltolide. Org. Lett. 2009, 11, 4700-4703.
    • (2009) Org. Lett. , vol.11 , pp. 4700-4703
    • Guinchard, X.1    Roulland, E.2
  • 61
    • 71549145618 scopus 로고    scopus 로고
    • Total Synthesis and Biological Evaluation of (+)-Neopeltolide and Its Analogues
    • Fuwa, H.; Saito, A.; Naito, S.; Konoki, K.; Yotsu-Yamashita, M.; Sasaki, M. Total Synthesis and Biological Evaluation of (+)-Neopeltolide and Its Analogues. Chem. Eur. J. 2009, 15, 12807-12818.
    • (2009) Chem. Eur. J. , vol.15 , pp. 12807-12818
    • Fuwa, H.1    Saito, A.2    Naito, S.3    Konoki, K.4    Yotsu-Yamashita, M.5    Sasaki, M.6
  • 62
    • 77951182592 scopus 로고    scopus 로고
    • A Concise Total Synthesis of (+)-Neopeltolide
    • Fuwa, H.; Saito, A.; Sasaki, M. A Concise Total Synthesis of (+)-Neopeltolide. Angew. Chem. Int. Ed. 2010, 49, 3041-3044.
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 3041-3044
    • Fuwa, H.1    Saito, A.2    Sasaki, M.3
  • 63
    • 77954244027 scopus 로고    scopus 로고
    • Total synthesis of neopeltolide and analogs
    • Cui, Y.; Tu, W.; Floreancig, P.E. Total synthesis of neopeltolide and analogs. Tetrahedron 2010, 66, 4867-4873.
    • (2010) Tetrahedron , vol.66 , pp. 4867-4873
    • Cui, Y.1    Tu, W.2    Floreancig, P.E.3
  • 64
    • 71049165179 scopus 로고    scopus 로고
    • A concise stereoselective formal total synthesis of the cytotoxic macrolide (+)-Neopeltolide via Prins cyclization
    • Yadav. J.S.; Kumar. G.G. A concise stereoselective formal total synthesis of the cytotoxic macrolide (+)-Neopeltolide via Prins cyclization. Tetrahedron 2010, 66, 480-487.
    • (2010) Tetrahedron , vol.66 , pp. 480-487
    • Yadav, J.S.1    Kumar, G.G.2
  • 65
    • 77955043068 scopus 로고    scopus 로고
    • Total Synthesis of Enigmazole A from Cinachyrella enigmatica. Bidirectional Bond Constructions with an Ambident 2,4-Disubstituted Oxazole Synthon
    • Skepper, C.K.; Quach, T.; Molinski, T.F. Total Synthesis of Enigmazole A from Cinachyrella enigmatica. Bidirectional Bond Constructions with an Ambident 2,4-Disubstituted Oxazole Synthon. J. Am. Chem. Soc. 2010, 132, 10286-10292.
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 10286-10292
    • Skepper, C.K.1    Quach, T.2    Molinski, T.F.3
  • 66
    • 41549092718 scopus 로고    scopus 로고
    • Total synthesis of (-)-ulapualide a, a novel tris-oxazole macrolide from marine nudibranchs, based on some biosynthesis speculation
    • Pattenden, G.; Ashweek, N.J.; Baker-Glenn, C.A.G.; Kempson, J.; Walker, G.M.; Yee, J.G.K. Total synthesis of (-)-ulapualide A, a novel tris-oxazole macrolide from marine nudibranchs, based on some biosynthesis speculation. Org. Biomol. Chem. 2008, 6, 1478-1497.
    • (2008) Org. Biomol. Chem. , vol.6 , pp. 1478-1497
    • Pattenden, G.1    Ashweek, N.J.2    Baker-Glenn, C.A.G.3    Kempson, J.4    Walker, G.M.5    Yee, J.G.K.6
  • 67
    • 34447265549 scopus 로고    scopus 로고
    • Total synthesis of (-)-ulapualide A: The danger of overdependence on NMR spectroscopy in assignment of stereochemistry
    • Pattenden, G.; Ashweek, N.J.; Baker-Glenn, C.A.G.; Walker, G.M.; Yee, J.G.K. Total synthesis of (-)-ulapualide A: The danger of overdependence on NMR spectroscopy in assignment of stereochemistry. Angew. Chem. Int. Ed. 2007, 46, 4359-4363.
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 4359-4363
    • Pattenden, G.1    Ashweek, N.J.2    Baker-Glenn, C.A.G.3    Walker, G.M.4    Yee, J.G.K.5
  • 71
    • 34147162771 scopus 로고    scopus 로고
    • The total synthesis of siphonazole, a structurally unusual bis-oxazole natural product
    • Linder, J.; Moody, C.J. The total synthesis of siphonazole, a structurally unusual bis-oxazole natural product. Chem. Commun. 2007, 1508-1509.
    • (2007) Chem. Commun. , pp. 1508-1509
    • Linder, J.1    Moody, C.J.2
  • 72
    • 58149177788 scopus 로고    scopus 로고
    • Total synthesis of siphonazole and its O-methyl derivative, structurally unusual bis-oxazole natural products
    • Linder, J.; Blake, A.J.; Moody, C.J. Total synthesis of siphonazole and its O-methyl derivative, structurally unusual bis-oxazole natural products Org. Biomol. Chem. 2008, 6, 3908-3916.
    • (2008) Org. Biomol. Chem. , vol.6 , pp. 3908-3916
    • Linder, J.1    Blake, A.J.2    Moody, C.J.3
  • 73
    • 72249118391 scopus 로고    scopus 로고
    • Development of an Oxazole Conjunctive Reagent and Application to the Total Synthesis of Siphonazoles
    • Zhang, J.; Polishchuk, E.A.; Chen, J.; Ciufolini, M.A. Development of an Oxazole Conjunctive Reagent and Application to the Total Synthesis of Siphonazoles. J. Org. Chem. 2009, 74, 9140-9151.
    • (2009) J. Org. Chem. , vol.74 , pp. 9140-9151
    • Zhang, J.1    Polishchuk, E.A.2    Chen, J.3    Ciufolini, M.A.4
  • 74
    • 74949139942 scopus 로고    scopus 로고
    • Total Synthesis of Bengazole A
    • Chandrasekhar, S.; Sudhakar, A. Total Synthesis of Bengazole A. Org. Lett. 2010, 12, 236-238.
    • (2010) Org. Lett. , vol.12 , pp. 236-238
    • Chandrasekhar, S.1    Sudhakar, A.2
  • 75
    • 69549091800 scopus 로고    scopus 로고
    • Total synthesis of the potent antifungal agents bengazole C and E
    • Enriquez-Garcia, A.; Ley, S.V. Total synthesis of the potent antifungal agents bengazole C and E. Collect. Czechoslovak Chem. Commun. 2009, 74, 887-900.
    • (2009) Collect. Czechoslovak Chem. Commun. , vol.74 , pp. 887-900
    • Enriquez-Garcia, A.1    Ley, S.V.2
  • 76
    • 34547467756 scopus 로고    scopus 로고
    • Total synthesis of potent antifungal marine bisoxazole natural products benzazoles A and B
    • Bull, J.A.; Balskus, E.P.; Horan, R.A.J.; Langner, M.; Ley, S.V. Total synthesis of potent antifungal marine bisoxazole natural products benzazoles A and B. Chem. Eur. J. 2007, 13, 5515-5538.
    • (2007) Chem. Eur. J. , vol.13 , pp. 5515-5538
    • Bull, J.A.1    Balskus, E.P.2    Horan, R.A.J.3    Langner, M.4    Ley, S.V.5
  • 80
    • 33847025693 scopus 로고    scopus 로고
    • Iminophosphorane-based preparation of 2,5-disubstituted oxazole derivatives: Synthesis of the marine alkaloid almazole C
    • Fresneda, P.M.; Castaneda, M.; Blug, M.; Molina, P. Iminophosphorane- based preparation of 2,5-disubstituted oxazole derivatives: synthesis of the marine alkaloid almazole C. Synlett 2007, 2, 324-326.
    • (2007) Synlett , vol.2 , pp. 324-326
    • Fresneda, P.M.1    Castaneda, M.2    Blug, M.3    Molina, P.4
  • 81
    • 0029969514 scopus 로고    scopus 로고
    • Almazole D, a New Type of Antibacterial 2,5-Disubstituted Oxazolic Dipeptide from a Red Alga of the Coast of Senegal
    • N'Diaye, I.; Guella, G.; Mancini, I.; Pietra, F. Almazole D, a New Type of Antibacterial 2,5-Disubstituted Oxazolic Dipeptide from a Red Alga of the Coast of Senegal. Tetrahedron Lett. 1996, 37, 3049-3050.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 3049-3050
    • N'Diaye, I.1    Guella, G.2    Mancini, I.3    Pietra, F.4
  • 82
    • 77954223668 scopus 로고    scopus 로고
    • Synthesis of 5-(3-indolyl) oxazole natural products. Structure revision of Almazole D
    • Miyake, F.; Hashimoto, M.; Tonsiengsom, S.; Yakushijin, K.; Horne, D.A. Synthesis of 5-(3-indolyl) oxazole natural products. Structure revision of Almazole D. Tetrahedron 2010, 66, 4888-4893.
    • (2010) Tetrahedron , vol.66 , pp. 4888-4893
    • Miyake, F.1    Hashimoto, M.2    Tonsiengsom, S.3    Yakushijin, K.4    Horne, D.A.5
  • 84
    • 39349108754 scopus 로고    scopus 로고
    • Synthesis and Biological Evaluation of Phorboxazole Congeners Leading to the Discovery and Preparative Scale Synthesis of (+)-Chlorophorboxazole a Possessing Picomolar Human Solid Tumor Cell Growth Inhibitory Activity
    • Smith, A.B., III; Razler, T.M.; Meis, R.M.; Pettit, G.R. Synthesis and Biological Evaluation of Phorboxazole Congeners Leading to the Discovery and Preparative Scale Synthesis of (+)-Chlorophorboxazole A Possessing Picomolar Human Solid Tumor Cell Growth Inhibitory Activity. J. Org. Chem. 2008, 73, 1201-1208.
    • (2008) J. Org. Chem. , vol.73 , pp. 1201-1208
    • Smith III, A.B.1    Razler, T.M.2    Meis, R.M.3    Pettit, G.R.4
  • 86
    • 38349048323 scopus 로고    scopus 로고
    • Structural investigation of westiellamide analogs
    • Haberhauer, G.; Drosdow, E.; Oeser, T.; Rominger, F. Structural investigation of westiellamide analogs. Tetrahedron 2008, 64, 1853-1859.
    • (2008) Tetrahedron , vol.64 , pp. 1853-1859
    • Haberhauer, G.1    Drosdow, E.2    Oeser, T.3    Rominger, F.4


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