메뉴 건너뛰기




Volumn 7, Issue 3, 2009, Pages 314-330

Recent synthetic studies leading to structural revisions of marine natural products

Author keywords

Marine natural product; Stereoselective; Structural revision; Synthesis

Indexed keywords

2 HYDROXYACETOPHENONE; 3 (4' CHLOROPHENYL)ISOCOUMARIN; 4' CHLOROAURONE; AMPHIDINOLIDE W; ANTINEOPLASTIC AGENT; BREVENAL; CALAFIANIN; CHLOROCHALCONE; CHLOROKETONE; DOLASTATIN; DOLASTATIN 19; ELATENYNE; HEMIBREVETOXIN B; MACROCYCLIC COMPOUND; METHYL N BOC 3 AMINOPENATANOATE; NATURAL PRODUCT; NEOPELTOLIDE; OBYANAMIDE; PALMEROLIDE A; PERICOSINE A; PERICOSINE B; PERICOSINE C; PERICOSINE D; TRIDACHIAHYDROPYRONE; UNCLASSIFIED DRUG;

EID: 70349488843     PISSN: None     EISSN: 16603397     Source Type: Journal    
DOI: 10.3390/md7030314     Document Type: Review
Times cited : (49)

References (54)
  • 1
    • 33645801979 scopus 로고    scopus 로고
    • Natural products from marine invertebrates and microbes as modulators of antitumor targets
    • DOI 10.2174/138945006776054960
    • Newman, D.J.; Cragg, G.M. Natural products from marine invertebrates and microbes as modulators of antitumor targets. Curr. Drug Targets 2006, 7, 279-304. (Pubitemid 43744847)
    • (2006) Current Drug Targets , vol.7 , Issue.3 , pp. 279-304
    • Newman, D.J.1    Cragg, G.M.2
  • 2
    • 3042617137 scopus 로고    scopus 로고
    • Advanced preclinical and clinical trials of natural products and related compounds from marine sources
    • Newman, D.J.; Cragg, G.M. Advanced preclinical and clinical trials of natural products and related compounds from marine sources. Curr. Med. Chem. 2004, 11, 1693-1713. (Pubitemid 38821339)
    • (2004) Current Medicinal Chemistry , vol.11 , Issue.13 , pp. 1693-1713
    • Newman, D.J.1    Cragg, G.M.2
  • 3
    • 17844399025 scopus 로고    scopus 로고
    • Natural products to drugs: Natural product derived compounds in clinical trials
    • Butler, M.S. Natural products to drugs: natural product derived compounds in clinical trials. Nat. Prod. Rep. 2005, 22, 162-195.
    • (2005) Nat. Prod. Rep. , vol.22 , pp. 162-195
    • Butler, M.S.1
  • 4
    • 26044483854 scopus 로고    scopus 로고
    • Synthetic study toward antitumour natural product pericosine a
    • DOI 10.1246/cl.2005.1062
    • Usami, Y.; Ueda, Y. Synthetic study toward antitumour natural product pericosine A. Chem. Lett. 2005, 34, 1062-1063. (Pubitemid 41405021)
    • (2005) Chemistry Letters , vol.34 , Issue.7 , pp. 1062-1063
    • Usami, Y.1    Ueda, Y.2
  • 5
    • 35548998674 scopus 로고    scopus 로고
    • Stereoselective syntheses of diastereomers of antitumor natural product pericosine a from (-)-quinic acid
    • DOI 10.1055/s-2007-990798
    • Usami, Y.; Ueda, Y. Stereoselective syntheses of diastereomers of antitumor natural product pericosine a from (-)-quinic acid. Synthesis 2007, 3219-3225. (Pubitemid 350013369)
    • (2007) Synthesis , Issue.20 , pp. 3219-3225
    • Usami, Y.1    Ueda, Y.2
  • 6
    • 33745698028 scopus 로고    scopus 로고
    • First total synthesis of (-)-pericosine a from (-)-shikimic acid: Structure Revision and determination of the absolute configuration of antitumor natural product pericosine a
    • Usami, Y.; Horibe, Y.; Takaoka, I.; Ichikawa, H.; Arimoto, M. First total synthesis of (-)-pericosine A from (-)-shikimic acid: Structure Revision and determination of the absolute configuration of antitumor natural product pericosine A. Synlett 2006, 1598-1600.
    • (2006) Synlett , pp. 1598-1600
    • Usami, Y.1    Horibe, Y.2    Takaoka, I.3    Ichikawa, H.4    Arimoto, M.5
  • 8
    • 41649115395 scopus 로고    scopus 로고
    • Synthetic efforts for stereo structure determination of cytotoxic marine natural product pericosines as metabolites of Periconia sp. from sea hare
    • Usami, Y.; Ichikawa, H.; Arimoto, M. Synthetic efforts for stereo structure determination of cytotoxic marine natural product pericosines as metabolites of Periconia sp. from sea hare. Int. J. Mol. Sci. 2008, 9, 401-421.
    • (2008) Int. J. Mol. Sci. , vol.9 , pp. 401-421
    • Usami, Y.1    Ichikawa, H.2    Arimoto, M.3
  • 9
    • 17844408197 scopus 로고    scopus 로고
    • Marine natural products: Synthetic aspects
    • DOI 10.1039/b407236g
    • Nicholas, G.M.; Phillips, A.J. Marine natural products: Synthetic aspects. Nat. Prod. Rep. 2005, 22, 144-161. (Pubitemid 40589044)
    • (2005) Natural Product Reports , vol.22 , Issue.2 , pp. 144-161
    • Nicholas, G.M.1    Phillips, A.J.2
  • 10
    • 33644970944 scopus 로고    scopus 로고
    • Marine natural products: Synthetic aspects
    • Nicholas, G.M.; Phillips, A.J. Marine natural products: Synthetic aspects. Nat. Prod. Rep. 2006, 23, 79-99.
    • (2006) Nat. Prod. Rep. , vol.23 , pp. 79-99
    • Nicholas, G.M.1    Phillips, A.J.2
  • 11
    • 33846924626 scopus 로고    scopus 로고
    • Marine natural products: Synthetic aspects
    • DOI 10.1039/b602832m
    • Morris, J.C.; Nicholas, G.M.; Phillips, A.J. Marine natural products: synthetic aspects. Nat. Prod. Rep. 2007, 24, 87-108. (Pubitemid 46238590)
    • (2007) Natural Product Reports , vol.24 , Issue.1 , pp. 87-108
    • Morris, J.C.1    Nicholas, G.M.2    Phillips, A.J.3
  • 12
    • 38849110033 scopus 로고    scopus 로고
    • Marine natural products: Synthetic aspects
    • Morris J.C.; Phillips A.J. Marine natural products: synthetic aspects. Nat. Prod. Rep. 2008, 25, 95-117.
    • (2008) Nat. Prod. Rep. , vol.25 , pp. 95-117
    • Morris, J.C.1    Phillips, A.J.2
  • 13
    • 59349102368 scopus 로고    scopus 로고
    • Marine natural products: Synthetic aspects
    • Morris, J.C.; Phillips, A.J. Marine natural products: synthetic aspects. Nat. Prod. Rep. 2009, 26, 245-265.
    • (2009) Nat. Prod. Rep. , vol.26 , pp. 245-265
    • Morris, J.C.1    Phillips, A.J.2
  • 14
    • 15444378803 scopus 로고    scopus 로고
    • Chasing molecules that were never there: Misassigned natural products and the role of chemical synthesis in modern structure elucidation
    • Nicolaou, K.C.; Snyder, S.A. Chasing molecules that were never there: Misassigned natural products and the role of chemical synthesis in modern structure elucidation. Angew. Chem. Int. Ed. 2005, 44, 1012-1044.
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 1012-1044
    • Nicolaou, K.C.1    Snyder, S.A.2
  • 15
    • 0027212254 scopus 로고
    • Palau'amine: A cytotoxic and immunosuppressive hexacyclic bisguanidine antibiotic from the sponge Stylotella agminata
    • Kinnel, R.B.; Gehrken, H.-P.; Scheuer, P.J. Palau'amine: A cytotoxic and immunosuppressive hexacyclic bisguanidine antibiotic from the sponge Stylotella agminata. J. Am. Chem. Soc. 1993, 115, 3376-3377.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 3376-3377
    • Kinnel, R.B.1    Gehrken, H.-P.2    Scheuer, P.J.3
  • 17
    • 0036158494 scopus 로고    scopus 로고
    • Isolation and structure determination of obyanamide, a novel cytotoxic cyclic depsipeptide from the marine cyanobacterium Lyngbya confervoides
    • Williams, P.G.; Yoshida, W.Y.; Moore, R.E.; Paul, V.J. Isolation and structure determination of obyanamide, a novel cytotoxic cyclic depsipeptide from the marine cyanobacterium Lyngbya confervoides. J. Nat. Prod. 2002, 65, 29-31.
    • (2002) J. Nat. Prod. , vol.65 , pp. 29-31
    • Williams, P.G.1    Yoshida, W.Y.2    Moore, R.E.3    Paul, V.J.4
  • 18
    • 33645337658 scopus 로고    scopus 로고
    • Synthesis of obyanamide, a marine cytotoxic cyclic depsipeptide
    • Zhang, W.; Song, N.; Li, Z.-Z.; Li, Y.-X. Synthesis of obyanamide, a marine cytotoxic cyclic depsipeptide. Chin. Chem. Lett. 2006, 17, 285-288.
    • (2006) Chin. Chem. Lett. , vol.17 , pp. 285-288
    • Zhang, W.1    Song, N.2    Li, Z.-Z.3    Li, Y.-X.4
  • 19
    • 33748202944 scopus 로고    scopus 로고
    • Total synthesis and reassignment of stereochemistry of obyanamide
    • DOI 10.1016/j.tet.2006.08.002, PII S0040402006012579
    • Zhang, W.; Ma, Z.-H.; Mei, D.; Li, C.-X.; Zhang, X.-L.; Li, Y.-X. Total synthesis and reassignment of stereochemistry of obyanamide. Tetrahedron 2006, 62, 9966-9972. (Pubitemid 44311167)
    • (2006) Tetrahedron , vol.62 , Issue.42 , pp. 9966-9972
    • Zhang, W.1    Ma, Z.-H.2    Mei, D.3    Li, C.-X.4    Zhang, X.-L.5    Li, Y.-X.6
  • 20
    • 0037039948 scopus 로고    scopus 로고
    • Amphidinolide W, a new 12-membered macrolide from dinoflagellate Amphidinium sp
    • Shimbo, K.; Tsuda, M.; Izui, N.; Kobayashi, J. Amphidinolide W, a new 12-membered macrolide from dinoflagellate Amphidinium sp. J. Org. Chem. 2002, 67, 1020-1023.
    • (2002) J. Org. Chem. , vol.67 , pp. 1020-1023
    • Shimbo, K.1    Tsuda, M.2    Izui, N.3    Kobayashi, J.4
  • 21
    • 1642288053 scopus 로고    scopus 로고
    • Total Synthesis and Structural Revision of (+)-Amphidinolide W
    • DOI 10.1021/ja049754u
    • Ghosh, A.K.; Gong, G. Total synthesis and structural revision of (+)-amphidinolide W. J. Am. Chem. Soc. 2004, 126, 3704-3705. (Pubitemid 38391852)
    • (2004) Journal of the American Chemical Society , vol.126 , Issue.12 , pp. 3704-3705
    • Ghosh, A.K.1    Gong, G.2
  • 22
    • 32144460995 scopus 로고    scopus 로고
    • Total synthesis and revision of C6 stereochemistry of (+)-amphidinolide W
    • DOI 10.1021/jo052181z
    • Ghosh, A.K.; Gong, G. Total synthesis and revision of C6 stereochemistry of (+)-amphidinolide W. J. Org. Chem. 2006, 71, 1085-1093. (Pubitemid 43209255)
    • (2006) Journal of Organic Chemistry , vol.71 , Issue.3 , pp. 1085-1093
    • Ghosh, A.K.1    Gong, G.2
  • 23
    • 33646554810 scopus 로고    scopus 로고
    • Palmerolide A, a cytotoxic macrolide from the antarctic tunicate Synoicum adareanum
    • Diyabalanage, T.; Amsler, C.D.; McClintock, J.B.; Baker, J. Palmerolide A, a cytotoxic macrolide from the antarctic tunicate Synoicum adareanum. J. Am. Chem. Soc. 2006, 128, 5630-5631.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 5630-5631
    • Diyabalanage, T.1    Amsler, C.D.2    McClintock, J.B.3    Baker, J.4
  • 24
    • 34249037678 scopus 로고    scopus 로고
    • Total synthesis and structure revision of the marine metabolite palmerolide a
    • DOI 10.1021/ja0715142
    • Jiang, X.; Liu, B.; Lebreton, S.; de Brabander, J.K. Total synthesis and structure revision of the marine metabolite palmerolide A. J. Am. Chem. Soc. 2007, 129, 6386-6387. (Pubitemid 46799331)
    • (2007) Journal of the American Chemical Society , vol.129 , Issue.20 , pp. 6386-6387
    • Jiang, X.1    Liu, B.2    Lebreton, S.3    De Brabander, J.K.4
  • 25
    • 34547805642 scopus 로고    scopus 로고
    • Total synthesis of the originally proposed and revised structures of palmerolide a
    • Nicolaou, K.C.; Guduru, R.; Sun, Y.-P.; Banerji, B.; Chen, D.Y.-K. Total synthesis of the originally proposed and revised structures of palmerolide A. Angew. Chem. Int. Ed. 2007, 46, 5896-5900.
    • (2007) Angew. Chem. Int. Ed. , vol.46 , pp. 5896-5900
    • Nicolaou, K.C.1    Guduru, R.2    Sun, Y.-P.3    Banerji, B.4    Chen, D.Y.-K.5
  • 26
    • 41449103344 scopus 로고    scopus 로고
    • Total synthesis of the originally proposed and revised structures of palmerolide a and isomers thereof
    • Nicolaou, K.C.; Sun, Y.-P.; Guduru, R.; Banerji, B.; Chen, D.Y.-K. Total synthesis of the originally proposed and revised structures of palmerolide A and isomers thereof. J. Am. Chem. Soc. 2008, 130, 3633-3644.
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 3633-3644
    • Nicolaou, K.C.1    Sun, Y.-P.2    Guduru, R.3    Banerji, B.4    Chen, D.Y.-K.5
  • 27
    • 4344668988 scopus 로고    scopus 로고
    • Antineoplastic agents. 510. Isolation and structure of dolastatin 19 from the Gulf of California sea hare Dolabella auricularia
    • Pettit, G.R.; Xu, J.-P.; Doubek, D.L.; Chapuis, J.-C.; Schmidt, J.M. Antineoplastic agents. 510. Isolation and structure of dolastatin 19 from the Gulf of California sea hare Dolabella auricularia. J. Nat. Prod. 2004, 67, 1252-1255.
    • (2004) J. Nat. Prod. , vol.67 , pp. 1252-1255
    • Pettit, G.R.1    Xu, J.-P.2    Doubek, D.L.3    Chapuis, J.-C.4    Schmidt, J.M.5
  • 28
    • 33744723813 scopus 로고    scopus 로고
    • Total synthesis and stereochemical reassignment of (+)-dolastatin 19
    • DOI 10.1021/ol060609q
    • Paterson, I.; Findlay, A.D.; Florence, G.J. Total synthesis and stereochemical reassignment of (+)-dolastatin 19. Org. Lett. 2006, 8, 2131-2134. (Pubitemid 43823628)
    • (2006) Organic Letters , vol.8 , Issue.10 , pp. 2131-2134
    • Paterson, I.1    Findlay, A.D.2    Florence, G.J.3
  • 31
    • 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
  • 34
    • 33746588648 scopus 로고    scopus 로고
    • Total synthesis of the proposed structure of brevenal
    • DOI 10.1021/ja062524q
    • Fuwa, H.; Ebine, M.; Sasaki, M. Total synthesis of the proposed structure of brevenal. J. Am. Chem. Soc. 2006, 128, 9648-9650. (Pubitemid 44147946)
    • (2006) Journal of the American Chemical Society , vol.128 , Issue.30 , pp. 9648-9650
    • Fuwa, H.1    Ebine, M.2    Sasaki, M.3
  • 35
    • 0001418722 scopus 로고
    • The structure of hemibrevetoxin-B; a new type of the Gulf of Mexico red tide organism
    • Prasad, A.V.K.; Shimizu, T. The structure of hemibrevetoxin-B; A new type of the Gulf of Mexico red tide organism. J. Am. Chem. Soc. 1989, 111, 6476-6477.
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 6476-6477
    • Prasad, A.V.K.1    Shimizu, T.2
  • 36
    • 33845963639 scopus 로고    scopus 로고
    • Total Synthesis, structure revision, and absolute configuration of (-)-brevenal
    • Fuwa, H.; Ebine, M.; Bourdelais, A.J.; Baden, D.G.; Sasaki, M. Total Synthesis, structure revision, and absolute configuration of (-)-brevenal. J. Am. Chem. Soc. 2006, 128, 16989-16999.
    • (2006) J. Am. Chem. Soc. , vol.128 , pp. 16989-16999
    • Fuwa, H.1    Ebine, M.2    Bourdelais, A.J.3    Baden, D.G.4    Sasaki, M.5
  • 37
    • 84969323584 scopus 로고
    • Elatenyne - A pyrano[3,2-b]pyranyl vinyl acetylene from the red alga Laurencia elata
    • Hall, J.G.; Reiss, J.A. Elatenyne - a pyrano[3,2-b]pyranyl vinyl acetylene from the red alga Laurencia elata. Aust. J. Chem. 1986, 39, 1401-1409.
    • (1986) Aust. J. Chem. , vol.39 , pp. 1401-1409
    • Hall, J.G.1    Reiss, J.A.2
  • 39
    • 33751003265 scopus 로고    scopus 로고
    • The changing faces of halogenated marine natural products: Total synthesis of the reported structures of elatenyne and an enyne from Laurencia majuscula
    • Sheldrake, H.M.; Jamieson, C.; Burton, J.W. The changing faces of halogenated marine natural products: total synthesis of the reported structures of elatenyne and an enyne from Laurencia majuscula. Angew. Chem. Int. Ed. 2006, 45, 7199-7202.
    • (2006) Angew. Chem. Int. Ed. , vol.45 , pp. 7199-7202
    • Sheldrake, H.M.1    Jamieson, C.2    Burton, J.W.3
  • 40
    • 58149154535 scopus 로고    scopus 로고
    • Synthesis of the originally proposed structures of elatenyne and an enyne from Laurencia majuscule
    • Sheldrake, H.M.; Jamieson, C.; Pascu, S.I.; Burton J.W. Synthesis of the originally proposed structures of elatenyne and an enyne from Laurencia majuscule. Org. Biomol. Chem. 2009, 7, 238-252.
    • (2009) Org. Biomol. Chem. , vol.7 , pp. 238-252
    • Sheldrake, H.M.1    Jamieson, C.2    Pascu, S.I.3    Burton, J.W.4
  • 41
    • 0033945102 scopus 로고    scopus 로고
    • Calafianin, a bromotyrosine derivative from the marine sponge Aplysina gerardogreeni
    • Encarnacion, R.D.; Sandoval, E.; Malmstrom, J.; Christophersen, C. Calafianin, a bromotyrosine derivative from the marine sponge Aplysina gerardogreeni. J. Nat. Prod. 2000, 63, 874-875.
    • (2000) J. Nat. Prod. , vol.63 , pp. 874-875
    • Encarnacion, R.D.1    Sandoval, E.2    Malmstrom, J.3    Christophersen, C.4
  • 42
    • 12344289555 scopus 로고    scopus 로고
    • Synthesis and structural revision of calafianin, a member of the spiroisoxazole family isolated from the marine sponge, Aplysina gerardogreeni
    • Ogamino, T.; Nishiyama, S. Synthesis and structural revision of calafianin, a member of the spiroisoxazole family isolated from the marine sponge, Aplysina gerardogreeni. Tetrahedron Lett. 2005, 46, 1083-1086.
    • (2005) Tetrahedron Lett. , vol.46 , pp. 1083-1086
    • Ogamino, T.1    Nishiyama, S.2
  • 43
    • 33750506090 scopus 로고    scopus 로고
    • Total synthesis, structural revision, and biological evaluation of calafianin, a marine spiroisoxazoline from the sponge, Aplysina gerardogreeni
    • DOI 10.1246/bcsj.79.134
    • Ogamino, T.; Obata, R.; Tomoda, H.; Nishiyama, S. Total synthesis, structural revision, and biological evaluation of calafianin, a marine spiroisoxazoline from the sponge, Aplysina gerardogreeni. Bull. Chem. Soc. Jpn. 2006, 79, 134-139. (Pubitemid 44661467)
    • (2006) Bulletin of the Chemical Society of Japan , vol.79 , Issue.1 , pp. 134-139
    • Ogamino, T.1    Obata, R.2    Tomoda, H.3    Nishiyama, S.4
  • 44
    • 33644959976 scopus 로고    scopus 로고
    • Total synthesis and stereochemical assignment of the spiroisoxazoline natural product (+)-calafianin
    • Bardhan, S.; Schmitt, D.C.; Porco, J.A., Jr. Total synthesis and stereochemical assignment of the spiroisoxazoline natural product (+)-calafianin. Org. Lett. 2006, 8, 927-930.
    • (2006) Org. Lett. , vol.8 , pp. 927-930
    • Bardhan, S.1    Schmitt, D.C.2    Porco Jr., J.A.3
  • 45
    • 0029989017 scopus 로고    scopus 로고
    • A new γ-dihydropyrone-propionate from the Caribbean sacoglossan Tridachia crispata
    • DOI 10.1016/0040-4039(96)00811-8
    • Gavagnin, M.; Mollo, E.; Cimino, G.; Ortea, J. A new γ- dihydropyrone-propionate from the caribbean sacoglossan Tridachia crispata. Tetrahedron Lett. 1996, 37, 4259-4262. (Pubitemid 26184367)
    • (1996) Tetrahedron Letters , vol.37 , Issue.24 , pp. 4259-4262
    • Gavagnin, M.1    Mollo, E.2    Cimino, G.3    Ortea, J.4
  • 46
    • 17844387575 scopus 로고    scopus 로고
    • Synthesis of the putative structure of tridachiahydropyrone
    • Jeffery, D.W.; Perkins, M.V.; White, J.M. Synthesis of the putative structure of tridachiahydropyrone. Org. Lett. 2005, 7, 1581-1584.
    • (2005) Org. Lett. , vol.7 , pp. 1581-1584
    • Jeffery, D.W.1    Perkins, M.V.2    White, J.M.3
  • 47
    • 55949098735 scopus 로고    scopus 로고
    • Biomimetic synthesis and structural revision of (±)- tridachiahydropyrone
    • Sharma, P.; Griffiths, N.; Moses, J.E. Biomimetic synthesis and structural revision of (±)-tridachiahydropyrone. Org. Lett. 2008, 10, 4025-4027.
    • (2008) Org. Lett. , vol.10 , pp. 4025-4027
    • Sharma, P.1    Griffiths, N.2    Moses, J.E.3
  • 49
    • 34249807357 scopus 로고    scopus 로고
    • Synthesis, structural revision, and biological activities of 4′-chloroaurone, a metabolite of marine brown alga Spatoglossum variabile
    • Venkateswarlu, S.; Panchagnula, G.K.; Gottumukkala A.L.; Subbaraju, G.V. Synthesis, structural revision, and biological activities of 4′-chloroaurone, a metabolite of marine brown alga Spatoglossum variabile. Tetrahedron 2007, 63, 6909-6914.
    • (2007) Tetrahedron , vol.63 , pp. 6909-6914
    • Venkateswarlu, S.1    Panchagnula, G.K.2    Gottumukkala, A.L.3    Subbaraju, G.V.4
  • 50
    • 0030726263 scopus 로고    scopus 로고
    • Novel antitumour metabolites produced by a fungal strain from a sea hare
    • PII S0040403997101988
    • Numata, A.; Iritani, M.; Yamada, T.; Minoura, K.; Matsumura, E.; Yamori, T.; Tsuruo, T. Novel antitumor metabolites produced by a fungal strain from a sea hare. Tetrahedron Lett. 1997, 38, 8215.8218. (Pubitemid 27508761)
    • (1997) Tetrahedron Letters , vol.38 , Issue.47 , pp. 8215-8218
    • Numata, A.1    Iritani, M.2    Yamada, T.3    Minoura, K.4    Matsumura, E.5    Yamori, T.6    Tsuruo, T.7
  • 51
    • 36749032164 scopus 로고    scopus 로고
    • Pericosines, antitumor metabolites from the sea hare-derived fungus Periconia byssoides. Structures and biological activities
    • Yamada, T.; Iritani, M.; Ohishi, H.; Tanaka, K.; Doi, M.; Minoura, K.; Numata, A. Pericosines, antitumor metabolites from the sea hare-derived fungus Periconia byssoides. Structures and biological activities. Org. Biomol. Chem. 2007, 5, 3979.3986.
    • (2007) Org. Biomol. Chem. , vol.5
    • Yamada, T.1    Iritani, M.2    Ohishi, H.3    Tanaka, K.4    Doi, M.5    Minoura, K.6    Numata, A.7
  • 52
    • 46449093611 scopus 로고    scopus 로고
    • Determination of the absolute configuration of the cytotoxic marine natural product pericosines D
    • Usami, Y.; Mizuki, K.; Ichikawa, H.; Arimoto, M. Determination of the absolute configuration of the cytotoxic marine natural product pericosines D. Tetrahedron: Asymmetry 2008, 19, 1460-1463.
    • (2008) Tetrahedron: Asymmetry , vol.19 , pp. 1460-1463
    • Usami, Y.1    Mizuki, K.2    Ichikawa, H.3    Arimoto, M.4
  • 53
    • 58049156062 scopus 로고    scopus 로고
    • Synthesis of (-)-pericosine B, the antipode of the cytotoxic marine natural product
    • Usami, Y.; Suzuki, K.; Mizuki, K.; Ichikawa, H.; Arimoto, M. Synthesis of (-)-pericosine B, the antipode of the cytotoxic marine natural product. Org. Biomol. Chem. 2009, 7, 315-318.
    • (2009) Org. Biomol. Chem. , vol.7 , pp. 315-318
    • Usami, Y.1    Suzuki, K.2    Mizuki, K.3    Ichikawa, H.4    Arimoto, M.5
  • 54
    • 67149125600 scopus 로고    scopus 로고
    • Facile and efficient synthesis of naturally occuring carbasugars (+)-pericosines A and C
    • Usami, Y.; Ohsugi, M.; Mizuki, K.; Ichikawa, H.; Arimoto, M. Facile and efficient synthesis of naturally occuring carbasugars (+)-pericosines A and C. Org. Lett. 2009, 11, 2699-2701.
    • (2009) Org. Lett. , vol.11 , pp. 2699-2701
    • Usami, Y.1    Ohsugi, M.2    Mizuki, K.3    Ichikawa, H.4    Arimoto, M.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.