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Volumn 10, Issue , 2014, Pages 34-114

Synthesis of five- and six-membered cyclic organic peroxides: Key transformations into peroxide ring-retaining products

Author keywords

1,2,4,5 tetraoxanes; 1,2,4 trioxanes; 1,2,4 trioxolanes; 1,2 dioxanes; 1,2 dioxenes; 1,2 dioxolanes; Cyclic peroxides; Ozonides

Indexed keywords


EID: 84891923837     PISSN: None     EISSN: 18605397     Source Type: Journal    
DOI: 10.3762/bjoc.10.6     Document Type: Review
Times cited : (84)

References (437)
  • 1
    • 0034964979 scopus 로고    scopus 로고
    • Recent advances in the chemistry of cyclic peroxides
    • DOI 10.2174/1385272013375346
    • McCullough, K. J.; Nojima, M. Curr. Org. Chem. 2001, 5, 601. doi:10.2174/1385272013375346 (Pubitemid 32544664)
    • (2001) Current Organic Chemistry , vol.5 , Issue.6 , pp. 601-636
    • McCullough, K.J.1    Nojima, M.2
  • 2
    • 39749101569 scopus 로고    scopus 로고
    • Synthesis of cyclic peroxides
    • Rappoport, Z., Ed.; John Wiley & Sons, Ltd: Chichester, 189-ff doi:10.1002/0470862769.ch5
    • Korshin, E. E.; Bachi, M. D. Synthesis of cyclic peroxides. In The Chemistry of Peroxides; Rappoport, Z., Ed.; John Wiley & Sons, Ltd: Chichester, 2006; Vol. 2, Part 1, pp 189 ff. doi:10.1002/0470862769.ch5
    • (2006) The Chemistry of Peroxides , vol.2 , Issue.PART 1
    • Korshin, E.E.1    Bachi, M.D.2
  • 4
    • 2542640961 scopus 로고    scopus 로고
    • A medicinal chemistry perspective on artemisinin and related endoperoxides
    • DOI 10.1021/jm030571c
    • O'Neill, P. M.; Posner, G. H. J. Med. Chem. 2004, 47, 2945. doi:10.1021/jm030571c (Pubitemid 38702690)
    • (2004) Journal of Medicinal Chemistry , vol.47 , Issue.12 , pp. 2945-2964
    • O'Neill, P.M.1    Posner, G.H.2
  • 7
    • 33746930206 scopus 로고    scopus 로고
    • Ozonolysis applications in drug synthesis
    • DOI 10.1021/cr040682z
    • Van Ornum, S. G.; Champeau, R. M.; Pariza, R. Chem. Rev. 2006, 106, 2990. doi:10.1021/cr040682z (Pubitemid 44193053)
    • (2006) Chemical Reviews , vol.106 , Issue.7 , pp. 2990-3001
    • Van Ornum, S.G.1    Champeau, R.M.2    Pariza, R.3
  • 8
    • 34249012765 scopus 로고    scopus 로고
    • New developments in synthetic peroxidic drugs as artemisinin mimics
    • DOI 10.1016/j.drudis.2007.04.009, PII S1359644607001870
    • Jefford, C. W. Drug Discovery Today 2007, 12, 487. doi:10.1016/j.drudis. 2007.04.009 (Pubitemid 46783690)
    • (2007) Drug Discovery Today , vol.12 , Issue.11-12 , pp. 487-495
    • Jefford, C.W.1
  • 9
    • 84857752045 scopus 로고    scopus 로고
    • doi:10.2174/156802612799362940
    • Jefford, C. W. Curr. Top. Med. Chem. 2012, 12, 373. doi:10.2174/ 156802612799362940
    • (2012) Curr. Top. Med. Chem. , vol.12 , pp. 373
    • Jefford, C.W.1
  • 10
    • 38949159992 scopus 로고    scopus 로고
    • Bioactive peroxides as potential therapeutic agents
    • DOI 10.1016/j.ejmech.2007.04.019, PII S0223523407002176
    • Dembitsky, V. M. Eur. J. Med. Chem. 2008, 43, 223. doi:10.1016/j.ejmech. 2007.04.019 (Pubitemid 351215614)
    • (2008) European Journal of Medicinal Chemistry , vol.43 , Issue.2 , pp. 223-251
    • Dembitsky, V.M.1
  • 13
    • 33845324499 scopus 로고    scopus 로고
    • Anticancer activity of natural and synthetic acetylenic lipids
    • DOI 10.1007/s11745-006-5044-3
    • Dembitsky, V. M. Lipids 2006, 41, 883. doi:10.1007/s11745-006-5044-3 (Pubitemid 44871578)
    • (2006) Lipids , vol.41 , Issue.10 , pp. 883-924
    • Dembitsky, V.M.1
  • 14
    • 27444447348 scopus 로고    scopus 로고
    • Astonishing diversity of natural surfactants: 5. Biologically active glycosides of aromatic metabolites
    • DOI 10.1007/s11745-005-1449-2, L9814
    • Dembitsky, V. M. Lipids 2005, 40, 869. doi:10.1007/s11745-005-1449-2 (Pubitemid 41531939)
    • (2005) Lipids , vol.40 , Issue.9 , pp. 869-900
    • Dembitsky, V.M.1
  • 15
    • 11844304234 scopus 로고    scopus 로고
    • doi:10.1002/cbdv.200490060
    • Dembitsky, V. M. Chem. Biodiversity 2004, 1, 673. doi:10.1002/cbdv. 200490060
    • (2004) Chem. Biodiversity , vol.1 , pp. 673
    • Dembitsky, V.M.1
  • 27
    • 36749074930 scopus 로고    scopus 로고
    • α-Substituted organic peroxides: Synthetic strategies for a biologically important class of gem-dihydroperoxide and perketal derivatives
    • DOI 10.1039/b711647k
    • Zmitek, K.; Zupan, M.; Iskra, J. Org. Biomol. Chem. 2007, 5, 3895. doi:10.1039/b711647k (Pubitemid 350214227)
    • (2007) Organic and Biomolecular Chemistry , vol.5 , Issue.24 , pp. 3895-3908
    • Zmitek, K.1    Zupan, M.2    Iskra, J.3
  • 28
    • 84891940167 scopus 로고    scopus 로고
    • Ph.D Thesis, University of Nebraska, Lincoln, NE, USA,; 195 ff. Diss. Abstr. Int., B 2003, 63 5855
    • Trullinger, T. K. Ph.D. Thesis, University of Nebraska, Lincoln, NE, USA, 2002; pp 195 ff. Diss. Abstr. Int., B 2003, 63, 5855.
    • (2002)
    • Trullinger, T.K.1
  • 29
    • 84891913560 scopus 로고    scopus 로고
    • Ph.D Thesis, University of Nebraska, Lincoln, NE, USA, 186 ff. Diss. Abstr. Int., B 2005, 66 281
    • Dai, P. Ph.D. Thesis, University of Nebraska, Lincoln, NE, USA, 2004; pp 186 ff. Diss. Abstr. Int., B 2005, 66, 281.
    • (2004)
    • Dai, P.1
  • 30
    • 84891911203 scopus 로고    scopus 로고
    • Ph.D Thesis, University of California, Irvine, CA, USA, 224 ff. Diss. Abstr. Int., B 2007, 67 6412
    • Ramirez, A. P. Ph.D. Thesis, University of California, Irvine, CA, USA, 2007; pp 224 ff. Diss. Abstr. Int., B 2007, 67, 6412.
    • (2007)
    • Ramirez, A.P.1
  • 31
    • 84891954754 scopus 로고    scopus 로고
    • Ph.D Thesis, University of Puerto Rico, Mayaguez, P. R., 159 ff. Diss. Abstr. Int., B 2010, 70 4186
    • Pena-Quevedo, A. J. Ph.D. Thesis, University of Puerto Rico, Mayaguez, P. R., 2009; pp 159 ff. Diss. Abstr. Int., B 2010, 70, 4186.
    • (2009)
    • Pena-Quevedo, A.J.1
  • 32
    • 84891928921 scopus 로고    scopus 로고
    • Ph.D Thesis, Boston University, Boston, MA, USA, 243 ff. Diss. Abstr. Int., B 1999, 60 193
    • Yao, G. Ph.D. Thesis, Boston University, Boston, MA, USA, 1999; pp 243 ff. Diss. Abstr. Int., B 1999, 60, 193.
    • (1999)
    • Yao, G.1
  • 41
    • 1542426931 scopus 로고
    • doi:10.1021/ar50143a002
    • Adam, W. Acc. Chem. Res. 1979, 12, 390. doi:10.1021/ar50143a002
    • (1979) Acc. Chem. Res. , vol.12 , pp. 390
    • Adam, W.1
  • 43
    • 34547517640 scopus 로고    scopus 로고
    • Rather exotic types of cyclic peroxides: Heteroatom dioxiranes
    • DOI 10.1021/cr0400717
    • Sawwan, N.; Greer, A. Chem. Rev. 2007, 107, 3247. doi:10.1021/cr0400717 (Pubitemid 47177111)
    • (2007) Chemical Reviews , vol.107 , Issue.7 , pp. 3247-3285
    • Sawwan, N.1    Greer, A.2
  • 45
    • 33845557937 scopus 로고
    • doi:10.1021/cr00041a005
    • Balci, M. Chem. Rev. 1981, 81, 91. doi:10.1021/cr00041a005
    • (1981) Chem. Rev. , vol.81 , pp. 91
    • Balci, M.1
  • 46
    • 0025959779 scopus 로고
    • doi:10.1016/S0040-4020(01)86413-9
    • Clennan, E. L. Tetrahedron 1991, 47, 1343. doi:10.1016/S0040-4020(01) 86413-9
    • (1991) Tetrahedron , vol.47 , pp. 1343
    • Clennan, E.L.1
  • 47
    • 43749120036 scopus 로고    scopus 로고
    • Stopping malaria parasites dead in their tracks
    • DOI 10.1038/nchembio0608-334, PII NCHEMBIO0608334
    • Doerig, C. D. Nat. Chem. Biol. 2008, 4, 334. doi:10.1038/nchembio0608-334 (Pubitemid 351694000)
    • (2008) Nature Chemical Biology , vol.4 , Issue.6 , pp. 334-335
    • Doerig, C.D.1
  • 51
    • 73849093637 scopus 로고    scopus 로고
    • doi:10.3390/molecules14125362
    • Liao, F. Molecules 2009, 14, 5362. doi:10.3390/molecules14125362
    • (2009) Molecules , vol.14 , pp. 5362
    • Liao, F.1
  • 55
    • 78650853998 scopus 로고    scopus 로고
    • doi:10.1007/s10156-010-0077-1
    • Kano, S. J. Infect. Chemother. 2010, 16, 375. doi:10.1007/s10156-010- 0077-1
    • (2010) J. Infect. Chemother. , vol.16 , pp. 375
    • Kano, S.1
  • 56
    • 77955680945 scopus 로고    scopus 로고
    • doi:10.3390/ph3072322
    • Li, Q.; Weina, P. Pharmaceuticals 2010, 3, 2322. doi:10.3390/ph3072322
    • (2010) Pharmaceuticals , vol.3 , pp. 2322
    • Li, Q.1    Weina, P.2
  • 57
    • 77954687214 scopus 로고    scopus 로고
    • doi:10.1039/c002196m
    • Wright, C. W. Nat. Prod. Rep. 2010, 27, 961. doi:10.1039/c002196m
    • (2010) Nat. Prod. Rep. , vol.27 , pp. 961
    • Wright, C.W.1
  • 63
    • 33745468499 scopus 로고    scopus 로고
    • Medicines for malaria venture: Sustaining antimalarial drug development
    • DOI 10.1016/j.pt.2006.05.011, PII S1471492206001255
    • Bathurst, I.; Hentschel, C. Trends Parasitol. 2006, 22, 301. doi:10.1016/j.pt.2006.05.011 (Pubitemid 43949613)
    • (2006) Trends in Parasitology , vol.22 , Issue.7 , pp. 301-307
    • Bathurst, I.1    Hentschel, C.2
  • 64
    • 42349104331 scopus 로고    scopus 로고
    • Qinghaosu (artemisinin): The price of success
    • DOI 10.1126/science.1155165
    • White, N. J. Science 2008, 320, 330. doi:10.1126/science.1155165 (Pubitemid 351555649)
    • (2008) Science , vol.320 , Issue.5874 , pp. 330-334
    • White, N.J.1
  • 65
    • 40849097597 scopus 로고    scopus 로고
    • Anticancer properties of artemisinin derivatives and their targeted delivery by transferrin conjugation
    • DOI 10.1016/j.ijpharm.2007.09.003, PII S0378517307007569
    • Nakase, I.; Lai, H.; Singh, N. P.; Sasaki, T. Int. J. Pharm. 2008, 354, 28. doi:10.1016/j.ijpharm.2007.09.003 (Pubitemid 351400327)
    • (2008) International Journal of Pharmaceutics , vol.354 , Issue.1-2 , pp. 28-33
    • Nakase, I.1    Lai, H.2    Singh, N.P.3    Sasaki, T.4
  • 68
    • 34247561355 scopus 로고    scopus 로고
    • Artesunate, artemether or quinine in severe Plasmodium falciparum malaria?
    • DOI 10.1586/14787210.5.2.199
    • Checkley, A. M.; Whitty, C. J. M. Expert Rev. Anti-Infect. Ther. 2007, 5, 199. doi:10.1586/14787210.5.2.199 (Pubitemid 46681739)
    • (2007) Expert Review of Anti-Infective Therapy , vol.5 , Issue.2 , pp. 199-204
    • Checkley, A.M.1    Whitty, C.J.M.2
  • 70
    • 34548126497 scopus 로고    scopus 로고
    • Drug discovery for malaria: A very challenging and timely endeavor
    • DOI 10.1016/j.cbpa.2007.05.038, PII S136759310700083X
    • Gelb, M. H. Curr. Opin. Chem. Biol. 2007, 11, 440. doi:10.1016/j.cbpa. 2007.05.038 (Pubitemid 47302852)
    • (2007) Current Opinion in Chemical Biology , vol.11 , Issue.4 , pp. 440-445
    • Gelb, M.H.1
  • 73
    • 22244463934 scopus 로고    scopus 로고
    • The future of antimalarials: Artemisinins and synthetic endoperoxides
    • DOI 10.1358/dof.2005.030.05.901987
    • Begue, J.-P.; Bonnet-Delpon, D. Drugs Future 2005, 30, 509. doi:10.1358/dof.2005.030.05.901987 (Pubitemid 40991872)
    • (2005) Drugs of the Future , vol.30 , Issue.5 , pp. 509-518
    • Begue, J.-P.1    Bonnet-Delpon, D.2
  • 85
    • 79952902065 scopus 로고    scopus 로고
    • doi:10.1016/j.exppara.2011.01.018
    • Sonnet, P.; Mullié, C. Exp. Parasitol. 2011, 128, 26. doi:10.1016/j.exppara.2011.01.018
    • (2011) Exp. Parasitol. , vol.128 , pp. 26
    • Sonnet, P.1    Mullié, C.2
  • 104
    • 4544359445 scopus 로고    scopus 로고
    • Structure-activity relationship of anti-malarial spongean peroxides having a 3-methoxy-1,2-dioxane structure
    • DOI 10.1016/j.bmc.2004.04.051, PII S0968089604006145
    • Kawanishi, M.; Kotoku, N.; Itagaki, S.; Horii, T.; Kobayashi, M. Bioorg. Med. Chem. 2004, 12, 5297. doi:10.1016/j.bmc.2004.04.051 105. (Pubitemid 39243950)
    • (2004) Bioorganic and Medicinal Chemistry , vol.12 , Issue.20 , pp. 5297-5307
    • Kawanishi, M.1    Kotoku, N.2    Itagaki, S.3    Horii, T.4    Kobayashi, M.5
  • 106
    • 33947102635 scopus 로고    scopus 로고
    • Cerium-catalyzed oxidative C-C bond forming reactions
    • DOI 10.1016/j.cattod.2006.11.008, PII S0920586106007127, The Catalytic Approach for the Synthesis if Fine Chemicals: Selected Papers of the 7th CAFC
    • Christoffers, J.; Werner, T.; Roessle, M. Catal. Today 2007, 121, 22. doi:10.1016/j.cattod.2006.11.008 (Pubitemid 46412214)
    • (2007) Catalysis Today , vol.121 , Issue.1-2 , pp. 22-26
    • Christoffers, J.1    Werner, T.2    Rossle, M.3
  • 118
    • 84891936583 scopus 로고
    • Patent Jpn. Kokai Tokkyo Koho JP 49061179 A, June 13
    • Kondo, K.; Matsumoto, M.; Hatsutani, M. Patent Jpn. Kokai Tokkyo Koho JP 49061179 A, June 13, 1974.
    • (1974)
    • Kondo, K.1    Matsumoto, M.2    Hatsutani, M.3
  • 124
    • 78649475176 scopus 로고    scopus 로고
    • doi:10.3390/molecules15117603
    • Brown, G. D. Molecules 2010, 15, 7603. doi:10.3390/molecules15117603
    • (2010) Molecules , vol.15 , pp. 7603
    • Brown, G.D.1
  • 125
    • 34347382573 scopus 로고    scopus 로고
    • Orally active antimalarials: Synthesis and bioevaluation of a new series of steroid-based 1,2,4-trioxanes against multi-drug resistant malaria in mice
    • DOI 10.1016/j.bmcl.2007.05.055, PII S0960894X07006233
    • Singh, C.; Sharma, U.; Saxena, G.; Puri, S. Bioorg. Med. Chem. Lett. 2007, 17, 4097. doi:10.1016/j.bmcl.2007.05.055 (Pubitemid 47023152)
    • (2007) Bioorganic and Medicinal Chemistry Letters , vol.17 , Issue.15 , pp. 4097-4101
    • Singh, C.1    Sharma, U.2    Saxena, G.3    Puri, Sunil.K.4
  • 137
    • 1842636383 scopus 로고    scopus 로고
    • Influence of stereoisomer of dispiro-1,2,4,5-tetraoxanes on their binding mode with heme and on antimalarial activity: Molecular docking studies
    • DOI 10.1016/j.bmc.2004.03.003, PII S0968089604001634
    • Tonmunphean, S.; Wijitkosoom, A.; Tantirungrotechai, Y. Bioorg. Med. Chem. 2004, 12, 2005. doi:10.1016/j.bmc.2004.03.003 (Pubitemid 38471694)
    • (2004) Bioorganic and Medicinal Chemistry , vol.12 , Issue.9 , pp. 2005-2012
    • Tonmunphean, S.1    Wijitkosoom, A.2    Tantirungrotechai, Y.3
  • 145
    • 0033594440 scopus 로고    scopus 로고
    • Synthesis and antimalarial activity of 11 dispiro-1,2,4,5-tetraoxane analogues of WR 148999. 7,8,15,16-tetraoxadispiro[5.2.5.2]hexadecanes substituted at the 1 and 10 positions with unsaturated and polar functional groups
    • DOI 10.1021/jm980698f
    • Dong, Y.; Matile, H.; Chollet, J.; Kaminsky, R.; Wood, J. K.; Vennerstrom, J. L. J. Med. Chem. 1999, 42, 1477. doi:10.1021/jm980698f (Pubitemid 29200885)
    • (1999) Journal of Medicinal Chemistry , vol.42 , Issue.8 , pp. 1477-1480
    • Dong, Y.1    Matile, H.2    Chollet, J.3    Kaminsky, R.4    Wood, J.K.5    Vennerstrom, J.L.6
  • 151
    • 77954582391 scopus 로고    scopus 로고
    • doi:10.1016/S0065-308X(10)73008-6
    • Keiser, J.; Utzinger, J. Adv. Parasitol. 2010, 73, 197. doi:10.1016/S0065-308X(10)73008-6
    • (2010) Adv. Parasitol. , vol.73 , pp. 197
    • Keiser, J.1    Utzinger, J.2
  • 160
    • 31944435391 scopus 로고    scopus 로고
    • Trematocidal activity of praziquantel and artemisinin derivatives: In vitro and in vivo investigations with adult Echinostoma caproni
    • DOI 10.1128/AAC.50.2.803-805.2006
    • Keiser, J.; Brun, R.; Fried, B.; Utzinger, J. Antimicrob. Agents Chemother. 2006, 50, 803. doi:10.1128/AAC.50.2.803-805.2006 (Pubitemid 43191007)
    • (2006) Antimicrobial Agents and Chemotherapy , vol.50 , Issue.2 , pp. 803-805
    • Keiser, J.1    Brun, R.2    Fried, B.3    Utzinger, J.4
  • 161
    • 70349974552 scopus 로고    scopus 로고
    • doi:10.1111/j.1365-3024.2009.01163.x
    • Vennervald, B. J.; Polman, K. Parasite Immunol. 2009, 31, 686. doi:10.1111/j.1365-3024.2009.01163.x
    • (2009) Parasite Immunol. , vol.31 , pp. 686
    • Vennervald, B.J.1    Polman, K.2
  • 166
    • 35448953068 scopus 로고    scopus 로고
    • Food-borne trematodiasis: Current chemotherapy and advances with artemisinins and synthetic trioxolanes
    • DOI 10.1016/j.pt.2007.07.012, PII S1471492207002486
    • Keiser, J.; Utzinger, J. Trends Parasitol. 2007, 23, 555. doi:10.1016/j.pt.2007.07.012 (Pubitemid 350030911)
    • (2007) Trends in Parasitology , vol.23 , Issue.11 , pp. 555-562
    • Keiser, J.1    Utzinger, J.2
  • 171
    • 77954033497 scopus 로고    scopus 로고
    • doi:10.1016/j.ijpara.2010.04.004
    • Brooker, S. Int. J. Parasitol. 2010, 40, 1137. doi:10.1016/j.ijpara.2010. 04.004
    • (2010) Int. J. Parasitol. , vol.40 , pp. 1137
    • Brooker, S.1
  • 172
    • 35848955628 scopus 로고    scopus 로고
    • Artemisinins and synthetic trioxolanes in the treatment of helminth infections
    • DOI 10.1097/QCO.0b013e3282f19ec4, PII 0000143220071200000009
    • Keiser, J.; Utzinger, J. Curr. Opin. Infect. Dis. 2007, 20, 605. doi:10.1097/QCO.0b013e3282f19ec4 (Pubitemid 350059520)
    • (2007) Current Opinion in Infectious Diseases , vol.20 , Issue.6 , pp. 605-612
    • Keiser, J.1    Utzinger, J.2
  • 179
    • 17744377209 scopus 로고    scopus 로고
    • Total syntheses of yingzhaosu A and of its C(14)-epimer including the first evaluation of their antimalarial and cytotoxic activities
    • DOI 10.1021/jo050074z
    • Szpilman, A. M.; Korshin, E. E.; Rozenberg, H.; Bachi, M. D. J. Org. Chem. 2005, 70, 3618. doi:10.1021/jo050074z (Pubitemid 40577573)
    • (2005) Journal of Organic Chemistry , vol.70 , Issue.9 , pp. 3618-3632
    • Szpilman, A.M.1    Korshin, E.E.2    Rozenberg, H.3    Bachi, M.D.4
  • 180
    • 27744604716 scopus 로고    scopus 로고
    • New bioactive cyclic peroxides from the Caribbean marine sponge Plakortis zyggompha
    • DOI 10.1016/j.tet.2005.09.077, PII S0040402005016728
    • Berrue, F.; Thomas, O. P.; Funel-Le Bon, C.; Reyes, F.; Amade, P. Tetrahedron 2005, 61, 11843. doi:10.1016/j.tet.2005.09.077 (Pubitemid 41635241)
    • (2005) Tetrahedron , vol.61 , Issue.50 , pp. 11843-11849
    • Berrue, F.1    Thomas, O.P.2    Bon, C.F.-L.3    Reyes, F.4    Amade, P.5
  • 181
    • 0027489190 scopus 로고
    • Three new cytotoxic metabolites from the marine sponge Plakortis halichondrioides
    • DOI 10.1021/np50100a027
    • Rudi, A.; Kashman, Y. J. Nat. Prod. 1993, 56, 1827. doi:10.1021/ np50100a027 (Pubitemid 23326308)
    • (1993) Journal of Natural Products (Lloydia) , vol.56 , Issue.10 , pp. 1827-1830
    • Rudi, A.1    Kashman, Y.2
  • 182
    • 0037149014 scopus 로고    scopus 로고
    • doi:10.1021/ol016943y
    • Yao, G.; Steliou, K. Org. Lett. 2002, 4, 485. doi:10.1021/ol016943y
    • (2002) Org. Lett. , vol.4 , pp. 485
    • Yao, G.1    Steliou, K.2
  • 183
    • 0037043564 scopus 로고    scopus 로고
    • doi:10.1021/ol026285x
    • Jung, M.; Ham, J.; Song, J. Org. Lett. 2002, 4, 2763. doi:10.1021/ol026285x
    • (2002) Org. Lett. , vol.4 , pp. 2763
    • Jung, M.1    Ham, J.2    Song, J.3
  • 195
    • 0033950843 scopus 로고    scopus 로고
    • Dimeric malarial drugs for enhanced activity
    • DOI 10.1016/S1359-6446(99)01453-1, PII S1359644699014531
    • Bradley, D. Drug Discovery Today 2000, 5, 44. doi:10.1016/S1359-6446(99) 01453-1 (Pubitemid 30084703)
    • (2000) Drug Discovery Today , vol.5 , Issue.2 , pp. 44-45
    • Bradley, D.1
  • 197
    • 0033083665 scopus 로고    scopus 로고
    • Peroxy natural products
    • DOI 10.1039/a705725c
    • Casteel, D. A. Nat. Prod. Rep. 1999, 16, 55. doi:10.1039/a705725c (Pubitemid 29092070)
    • (1999) Natural Product Reports , vol.16 , Issue.1 , pp. 55-73
    • Casteel, D.A.1
  • 198
    • 0026905982 scopus 로고
    • doi:10.1039/np9920900289
    • Casteel, D. A. Nat. Prod. Rep. 1992, 9, 289. doi:10.1039/np9920900289
    • (1992) Nat. Prod. Rep. , vol.9 , pp. 289
    • Casteel, D.A.1
  • 208
    • 0038101523 scopus 로고    scopus 로고
    • 4,9]tetradecane and derivatives with in vitro activity against Plasmodium falciparum, Trypanasoma b brucei, Trypanasoma cruzi, and Leishmaniasis infantum
    • DOI 10.1016/S0960-894X(03)00326-3
    • Howarth, J.; Wilson, D. Bioorg. Med. Chem. Lett. 2003, 13, 2013. doi:10.1016/S0960-894X(03)00326-3 (Pubitemid 36638401)
    • (2003) Bioorganic and Medicinal Chemistry Letters , vol.13 , Issue.12 , pp. 2013-2015
    • Howarth, J.1    Wilson, D.2
  • 215
    • 0038176459 scopus 로고    scopus 로고
    • Oxidation, epoxidation and sulfoxidation reactions catalysed by haloperoxidases
    • DOI 10.1016/S0040-4020(03)00701-4
    • Dembitsky, V. M. Tetrahedron 2003, 59, 4701. doi:10.1016/S0040-4020(03) 00701-4 (Pubitemid 36695117)
    • (2003) Tetrahedron , vol.59 , Issue.26 , pp. 4701-4720
    • Dembitsky, V.M.1
  • 219
    • 0036119159 scopus 로고    scopus 로고
    • Natural halogenated fatty acids: Their analogues and derivatives
    • DOI 10.1016/S0163-7827(02)00003-6, PII S0163782702000036
    • Dembitsky, V. M.; Srebnik, M. Prog. Lipid Res. 2002, 41, 315. doi:10.1016/S0163-7827(02)00003-6 (Pubitemid 34218149)
    • (2002) Progress in Lipid Research , vol.41 , Issue.4 , pp. 315-367
    • Dembitsky, V.M.1    Srebnik, M.2
  • 225
    • 0036113491 scopus 로고    scopus 로고
    • Relationships between molecular properties and antimycobacterial activities of steroids
    • DOI 10.1080/10575630290020000
    • Rugutt, J. K.; Rugutt, K. J. Nat. Prod. Lett. 2002, 16, 107. doi:10.1080/10575630290020000 (Pubitemid 34406481)
    • (2002) Natural Product Letters , vol.16 , Issue.2 , pp. 107-113
    • Rugutt, K.1    Rugutt, J.2
  • 229
    • 0034677832 scopus 로고    scopus 로고
    • Regioselectivity in the ene reaction of singlet oxygen with alkenes
    • DOI 10.1016/S0040-4020(99)00950-3, PII S0040402099009503
    • Stratakis, M.; Orfanopoulos, M. Tetrahedron 2000, 56, 1595. doi:10.1016/S0040-4020(99)00950-3 (Pubitemid 30190426)
    • (2000) Tetrahedron , vol.56 , Issue.12 , pp. 1595-1615
    • Stratakis, M.1    Orfanopoulos, M.2
  • 230
    • 20444464941 scopus 로고    scopus 로고
    • Advances in singlet oxygen chemistry
    • DOI 10.1016/j.tet.2005.04.017, PII S0040402005006629
    • Clennan, E. L.; Pace, A. Tetrahedron 2005, 61, 6665. doi:10.1016/j.tet. 2005.04.017 (Pubitemid 40823014)
    • (2005) Tetrahedron , vol.61 , Issue.28 , pp. 6665-6691
    • Clennan, E.L.1    Pace, A.2
  • 232
    • 0037179169 scopus 로고    scopus 로고
    • Synthesis of cardamom peroxide analogues by radical cyclization of hydroperoxyalkenes
    • DOI 10.1016/S0040-4039(02)01122-X, PII S004040390201122X
    • Cointeaux, L.; Berrien, J.-F.; Mayrargue, J. Tetrahedron Lett. 2002, 43, 6275. doi:10.1016/S0040-4039(02)01122-X (Pubitemid 34876786)
    • (2002) Tetrahedron Letters , vol.43 , Issue.35 , pp. 6275-6277
    • Cointeaux, L.1    Berrien, J.-F.2    Mayrargue, J.3
  • 233
    • 0034625912 scopus 로고    scopus 로고
    • Diastereoselective and regioselective singlet-oxygen ene reaction of oxazolidine-substituted alkenes: Control through hydrogen bonding mediated by the urea functionality of chiral auxiliaries [10]
    • DOI 10.1021/ja001113l
    • Adam, W.; Peters, K.; Peters, E.-M.; Schambony, S. J. Am. Chem. Soc. 2000, 122, 7610. doi:10.1021/ja001113l (Pubitemid 30641567)
    • (2000) Journal of the American Chemical Society , vol.122 , Issue.31 , pp. 7610-7611
    • Adam, W.1    Peters, K.2    Peters, E.-M.3    Schambony, S.B.4
  • 234
    • 0035078135 scopus 로고    scopus 로고
    • Preparation of 2,3-epoxycycloalkanones from bicyclo[n.1.0]Alkan-1-ols
    • DOI 10.1081/SCC-100000523
    • Barnier, J.-P.; Morisson, V.; Blanco, L. Synth. Commun. 2001, 31, 349. doi:10.1081/SCC-100000523 (Pubitemid 32231813)
    • (2001) Synthetic Communications , vol.31 , Issue.3 , pp. 349-357
    • Barnier, J.-P.1    Morisson, V.2    Blanco, L.3
  • 237
    • 0034780473 scopus 로고    scopus 로고
    • doi:10.1002 1099-0690 (200110) 2001:20〈3811::AID-EJOC3811〉3.0. CO;2-6
    • Wimalasena, K.; Wickman, H. B.; Mahindaratne, M. P. D. Eur. J. Org. Chem. 2001, 3811. doi:10.1002/1099-0690(200110)2001:20〈3811::AID- EJOC3811〉3.0.CO;2-6
    • (2001) Eur. J. Org. Chem. , vol.3811
    • Wimalasena, K.1    Wickman, H.B.2    Mahindaratne, M.P.D.3
  • 240
    • 34249028222 scopus 로고    scopus 로고
    • Synthetic studies toward plakortide e: Application of the feldman oxygenation to synthesis of highly substituted 1,2-dioxolanes
    • DOI 10.1016/j.tet.2007.02.121, PII S0040402007003638, Tetrahedron 50th Anniversary Symposium-in-Print (Part 2)
    • Zhao, Q.; Wong, H. N. C. Tetrahedron 2007, 63, 6296. doi:10.1016/j.tet. 2007.02.121 (Pubitemid 46782882)
    • (2007) Tetrahedron , vol.63 , Issue.27 , pp. 6296-6305
    • Zhao, Q.1    Wong, H.N.C.2
  • 242
    • 0035955840 scopus 로고    scopus 로고
    • 1,3-Bis(4-methoxyphenyl)cyclohexane-1,3-diyl cation radical: Divergent reactivity depending upon electron-transfer conditions
    • DOI 10.1016/S0040-4039(01)01786-5, PII S0040403901017865
    • Ikeda, H.; Hoshi, Y.; Miyashi, T. Tetrahedron Lett. 2001, 42, 8485. doi:10.1016/S0040-4039(01)01786-5 (Pubitemid 33043929)
    • (2001) Tetrahedron Letters , vol.42 , Issue.48 , pp. 8485-8488
    • Ikeda, H.1    Hoshi, Y.2    Miyashi, T.3
  • 243
    • 33747419905 scopus 로고    scopus 로고
    • A matrix isolation study of 2-isopropylidenecyclopentane-1,3-diyl (Berson-type diradical)
    • DOI 10.1021/jo060587l
    • Abe, M.; Kawanami, S.; Masuyama, A.; Hayashi, T. J. Org. Chem. 2006, 71, 6607. doi:10.1021/jo060587l (Pubitemid 44252452)
    • (2006) Journal of Organic Chemistry , vol.71 , Issue.17 , pp. 6607-6610
    • Abe, M.1    Kawanami, S.2    Masuyama, A.3    Hayashi, T.4
  • 244
    • 84857812665 scopus 로고    scopus 로고
    • doi:10.1021/jo300297u
    • Gbur, R. K.; Little, R. D. J. Org. Chem. 2012, 77, 2134-2141. doi:10.1021/jo300297u
    • (2012) J. Org. Chem. , vol.77 , pp. 2134-2141
    • Gbur, R.K.1    Little, R.D.2
  • 245
    • 63049100535 scopus 로고    scopus 로고
    • doi:10.1016/j.tet.2009.02.045
    • Tsubusaki, T.; Nishino, H. Tetrahedron 2009, 65, 3745. doi:10.1016/j.tet.2009.02.045
    • (2009) Tetrahedron , vol.65 , pp. 3745
    • Tsubusaki, T.1    Nishino, H.2
  • 247
    • 0001695182 scopus 로고
    • doi:10.1246/bcsj.63.1305
    • Isayama, S. Bull. Chem. Soc. Jpn. 1990, 63, 1305. doi:10.1246/bcsj.63. 1305
    • (1990) Bull. Chem. Soc. Jpn. , vol.63 , pp. 1305
    • Isayama, S.1
  • 250
    • 26444510168 scopus 로고    scopus 로고
    • Intramolecular reactions of hydroperoxides and oxetanes: Stereoselective synthesis of 1,2-dioxolanes and 1,2-dioxanes
    • DOI 10.1021/ol051407h
    • Dai, P.; Dussault, P. H. Org. Lett. 2005, 7, 4333. doi:10.1021/ol051407h (Pubitemid 41436640)
    • (2005) Organic Letters , vol.7 , Issue.20 , pp. 4333-4335
    • Dai, P.1    Dussault, P.H.2
  • 251
    • 84859608304 scopus 로고    scopus 로고
    • doi:10.1016/j.tet.2012.03.024
    • Barnych, B.; Vatèle, J.-M. Tetrahedron 2012, 68, 3717. doi:10.1016/j.tet.2012.03.024
    • (2012) Tetrahedron , vol.68 , pp. 3717
    • Barnych, B.1    Vatèle, J.-M.2
  • 253
    • 29544451140 scopus 로고    scopus 로고
    • Synthesis of trans-1,8,12,13-tetraoxadispiro[4.1.4.2]-tridecanes - A new class of peroxides
    • DOI 10.1016/j.tetlet.2005.11.107, PII S0040403905025712
    • Kumar, D. N.; Sudhakar, N.; Rao, B. V.; Kishore, K. H.; Murty, U. S. Tetrahedron Lett. 2006, 47, 771. doi:10.1016/j.tetlet.2005.11.107 (Pubitemid 43014809)
    • (2006) Tetrahedron Letters , vol.47 , Issue.5 , pp. 771-774
    • Naveen Kumar, D.1    Sudhakar, N.2    Rao, B.V.3    Kishore, K.H.4    Murty, U.S.5
  • 259
    • 27144520561 scopus 로고    scopus 로고
    • Synthesis of 1,2-dioxolanes by annulation reactions of peroxycarbenium ions with alkenes
    • DOI 10.1021/ol051703u
    • Ramirez, A.; Woerpel, K. A. Org. Lett. 2005, 7, 4617. doi:10.1021/ol051703u (Pubitemid 41507055)
    • (2005) Organic Letters , vol.7 , Issue.21 , pp. 4617-4620
    • Ramirez, A.1    Woerpel, K.A.2
  • 266
    • 33646455613 scopus 로고    scopus 로고
    • An intramolecular substitution of hydroperoxy-endoperoxide to a bis-endoperoxide
    • DOI 10.1021/ol060272s
    • Kishali, N.; Sahin, E.; Kara, Y. Org. Lett. 2006, 8, 1791. doi:10.1021/ol060272s (Pubitemid 43692160)
    • (2006) Organic Letters , vol.8 , Issue.9 , pp. 1791-1793
    • Kishali, N.1    Sahin, E.2    Kara, Y.3
  • 267
    • 4544295366 scopus 로고    scopus 로고
    • Curtius rearrangement and Wolff homologation of functionalized peroxides
    • DOI 10.1016/j.tetlet.2004.08.059, PII S0040403904017332
    • Dussault, P. H.; Xu, C. Tetrahedron Lett. 2004, 45, 7455. doi:10.1016/j.tetlet.2004.08.059 (Pubitemid 39213952)
    • (2004) Tetrahedron Letters , vol.45 , Issue.40 , pp. 7455-7457
    • Dussault, P.H.1    Xu, C.2
  • 269
    • 0343614014 scopus 로고    scopus 로고
    • doi:10.1002 (SICI) 1099-0690 (199808) 1998:8〈1625::AID- EJOC1625〉 3.0.CO;2-L
    • Geletneky, C.; Berger, S. Eur. J. Org. Chem. 1998, 1625. doi:10.1002/(SICI)1099-0690(199808)1998:8〈1625::AID-EJOC1625〉 3.0.CO;2-L
    • (1998) Eur. J. Org. Chem. , vol.1625
    • Geletneky, C.1    Berger, S.2
  • 276
    • 20644472226 scopus 로고    scopus 로고
    • doi:10.1002 1099-0690 (200105) 2001:10〈1899::AID-EJOC1899〉3.0.C O;2-L
    • Jung, I. C. Eur. J. Org. Chem. 2001, 1899. doi:10.1002/1099-0690(200105) 2001:10〈1899::AID-EJOC1899〉3.0.C O;2-L
    • (2001) Eur. J. Org. Chem. , vol.1899
    • Jung, I.C.1
  • 277
  • 279
    • 0037131236 scopus 로고    scopus 로고
    • Synthesis of a carbon analogue of N-acetylmannosamine via acetolysis on a relatively stable ozonide
    • DOI 10.1021/jo020362k
    • Chen, L.; Wiemer, D. F. J. Org. Chem. 2002, 67, 7561. doi:10.1021/jo020362k (Pubitemid 35176416)
    • (2002) Journal of Organic Chemistry , vol.67 , Issue.21 , pp. 7561-7564
    • Chen, L.1    Wiemer, D.F.2
  • 283
    • 4644292954 scopus 로고    scopus 로고
    • Ozonolyse von enolethern. 10. Mitteilung. Ozonisierung von enolethern aus 1,2- und 1,3-dicarbonyl-verbindungen: Direkte quantitative synthese von phthalonsaure-anhydrid
    • DOI 10.1002/hlca.200490182
    • Schank, K.; Beck, H.; Pistorius, S. Helv. Chim. Acta 2004, 87, 2025. doi:10.1002/hlca.200490182 (Pubitemid 39265836)
    • (2004) Helvetica Chimica Acta , vol.87 , Issue.8 , pp. 2025-2049
    • Schank, K.1    Beck, H.2    Pistorius, S.3
  • 286
    • 33745556903 scopus 로고    scopus 로고
    • Total synthesis of (±)-paeonilide
    • DOI 10.1021/ol060382z
    • Wang, C.; Liu, J.; Ji, Y.; Zhao, J.; Li, L.; Zhang, H. Org. Lett. 2006, 8, 2479. doi:10.1021/ol060382z (Pubitemid 43980422)
    • (2006) Organic Letters , vol.8 , Issue.12 , pp. 2479-2481
    • Wang, C.1    Liu, J.2    Ji, Y.3    Zhao, J.4    Li, L.5    Zhang, H.6
  • 287
    • 33746931551 scopus 로고    scopus 로고
    • Fragmentation of carbonyl oxides by N-oxides: An improved approach to alkene ozonolysis
    • DOI 10.1021/ol061001k
    • Schwartz, C.; Raible, J.; Mott, K.; Dussault, P. H. Org. Lett. 2006, 8, 3199. doi:10.1021/ol061001k (Pubitemid 44187415)
    • (2006) Organic Letters , vol.8 , Issue.15 , pp. 3199-3201
    • Schwartz, C.1    Raible, J.2    Mott, K.3    Dussault, P.H.4
  • 288
    • 33749242465 scopus 로고    scopus 로고
    • 'Reductive ozonolysis' via a new fragmentation of carbonyl oxides
    • DOI 10.1016/j.tet.2006.08.092, PII S0040402006014190, Organic Chemistry of Singlet Oxygen
    • Schwartz, C.; Raible, J.; Mott, K.; Dussault, P. H. Tetrahedron 2006, 62, 10747. doi:10.1016/j.tet.2006.08.092 (Pubitemid 44486341)
    • (2006) Tetrahedron , vol.62 , Issue.46 , pp. 10747-10752
    • Schwartz, C.1    Raible, J.2    Mott, K.3    Dussault, P.H.4
  • 289
    • 45249113717 scopus 로고    scopus 로고
    • Ozonolysis in solvent/water mixtures: Direct conversion of alkenes to aldehydes and ketones
    • DOI 10.1021/jo800323x
    • Schiaffo, C. E.; Dussault, P. H. J. Org. Chem. 2008, 73, 4688. doi:10.1021/jo800323x (Pubitemid 351842490)
    • (2008) Journal of Organic Chemistry , vol.73 , Issue.12 , pp. 4688-4690
    • Schiaffo, C.E.1    Dussault, P.H.2
  • 291
    • 0002233075 scopus 로고    scopus 로고
    • 10.1002 (SICI) 1099-0690 (200001) 2000:2〈335::AID-EJOC335〉3.0 .CO;2-2
    • Shin, H. S.; Lee, C.; Lee, J. Y.; Huh, T. S. Eur. J. Org. Chem. 2000, 335. doi:10.1002/(SICI)1099-0690(200001)2000:2〈335::AID-EJOC335〉3.0 .CO;2-2
    • (2000) Eur. J. Org. Chem. , pp. 335
    • Shin, H.S.1    Lee, C.2    Lee, J.Y.3    Huh, T.S.4
  • 292
    • 0034864753 scopus 로고    scopus 로고
    • doi:10.1002 1099-0690 (200108) 2001:16〈3083::AID-EJOC3083〉3.0.C O;2-K
    • Park, S. H.; Lee, J. Y.; Huh, T. S. Eur. J. Org. Chem. 2001, 3083. doi:10.1002/1099-0690(200108)2001:16〈3083::AID-EJOC3083〉3.0.C O;2-K
    • (2001) Eur. J. Org. Chem. , pp. 3083
    • Park, S.H.1    Lee, J.Y.2    Huh, T.S.3
  • 293
    • 0037185445 scopus 로고    scopus 로고
    • Ozonolyses of 1-alkyl-substituted 1-tert-butylethylenes and highly methylated methylenecycloalkanes. The influence of the substituent steric bulk on the direction of cleavage of the primary ozonides
    • DOI 10.1016/S0040-4020(01)01183-8, PII S0040402001011838
    • Kawamura, S.-i.; Yamakoshi, H.; Abe, M.; Masuyama, A.; Nojima, M. Tetrahedron 2002, 58, 891. doi:10.1016/S0040-4020(01)01183-8 (Pubitemid 34093835)
    • (2002) Tetrahedron , vol.58 , Issue.5 , pp. 891-896
    • Kawamura, S.-I.1    Yamakoshi, H.2    Abe, M.3    Masuyama, A.4    Nojima, M.5
  • 297
    • 4644291531 scopus 로고    scopus 로고
    • Synthesis of tetrasubstituted ozonides by the Griesbaum coozonolysis reaction: Diastereoselectivity and functional group transformations by post-ozonolysis reactions
    • DOI 10.1021/jo040171c
    • Tang, Y.; Dong, Y.; Karle, J. M.; DiTusa, C. A.; Vennerstrom, J. L. J. Org. Chem. 2004, 69, 6470. doi:10.1021/jo040171c (Pubitemid 39296257)
    • (2004) Journal of Organic Chemistry , vol.69 , Issue.19 , pp. 6470-6473
    • Tang, Y.1    Dong, Y.2    Karle, J.M.3    DiTusa, C.A.4    Vennerstrom, J.L.5
  • 299
    • 0035945029 scopus 로고    scopus 로고
    • Formation of 1,2,4-trioxolanes via 9,10-dicyanoanthracene(DCA)-sensitized photo-oxygenation of 2,2-diaryl-3-(2,2-diarylvinyl)oxiranes
    • DOI 10.1016/S0040-4039(01)01972-4, PII S0040403901019724
    • Kamata, M.; Komatsu, K.-i.; Akaba, R. Tetrahedron Lett. 2001, 42, 9203. doi:10.1016/S0040-4039(01)01972-4 (Pubitemid 33152885)
    • (2001) Tetrahedron Letters , vol.42 , Issue.52 , pp. 9203-9206
    • Kamata, M.1    Komatsu, K.-I.2    Akaba, R.3
  • 301
    • 0037060948 scopus 로고    scopus 로고
    • Synthesis, Fe(II)-induced degradation, and antimalarial activities of 1,5-diaryl-6,7-dioxabicyclo[3.2.2]nonanes: Direct evidence for nucleophilic O-1,2-aryl shifts
    • DOI 10.1016/S0040-4039(02)00166-1, PII S0040403902001661
    • Kamata, M.; Ohta, M.; Komatsu, K.-i.; Kim, H.-S.; Wataya, Y. Tetrahedron Lett. 2002, 43, 2063. doi:10.1016/S0040-4039(02)00166-1 (Pubitemid 34188524)
    • (2002) Tetrahedron Letters , vol.43 , Issue.11 , pp. 2063-2067
    • Kamata, M.1    Ohta, M.2    Komatsu, K.-I.3    Kim, H.-S.4    Wataya, Y.5
  • 303
    • 33746171070 scopus 로고    scopus 로고
    • Total syntheses of hexacyclinol, 5-epi-hexacyclinol, and desoxohexacyclinol unveil an antimalarial prodrug motif
    • DOI 10.1002/anie.200504033
    • La Clair, J. J. Angew. Chem., Int. Ed. 2006, 45, 2769. doi:10.1002/anie.200504033 (Pubitemid 44099103)
    • (2006) Angewandte Chemie - International Edition , vol.45 , Issue.17 , pp. 2769-2773
    • La Clair, J.J.1
  • 304
    • 56949104307 scopus 로고    scopus 로고
    • doi:10.1016/j.tetlet.2008.10.094
    • Griesbeck, A. G.; Cho, M. Tetrahedron Lett. 2009, 50, 121. doi:10.1016/j.tetlet.2008.10.094
    • (2009) Tetrahedron Lett. , vol.50 , pp. 121
    • Griesbeck, A.G.1    Cho, M.2
  • 306
    • 0035185613 scopus 로고    scopus 로고
    • Catalytic oxidation of 4-piperidone-3-carboxylates with manganese(III) acetate in the presence of 1,1-disubstituted
    • DOI 10.1016/S0040-4039(00)01884-0, PII S0040403900018840
    • Kumabe, R.; Nishino, H.; Yasutake, M.; Nguyen, V.-H.; Kurosawa, K. Tetrahedron Lett. 2001, 42, 69. doi:10.1016/S0040-4039(00)01884-0 (Pubitemid 32011708)
    • (2001) Tetrahedron Letters , vol.42 , Issue.1 , pp. 69-72
    • Kumabe, R.1    Nishino, H.2    Yasutake, M.3    Nguyen, V.-H.4    Kurosawa, K.5
  • 308
    • 28444466608 scopus 로고    scopus 로고
    • Cerium-catalyzed, aerobic oxidative synthesis of 1,2-dioxane derivatives from styrene and their fragmentation into 1,4-dicarbonyl compounds
    • DOI 10.1002/ejoc.200500487
    • Rössle, M.; Werner, T.; Frey, W.; Christoffers, J. Eur. J. Org. Chem. 2005, 5031. doi:10.1002/ejoc.200500487 (Pubitemid 41736457)
    • (2005) European Journal of Organic Chemistry , Issue.23 , pp. 5031-5038
    • Rossle, M.1    Werner, T.2    Frey, W.3    Christoffers, J.4
  • 309
    • 0347418220 scopus 로고    scopus 로고
    • A unique peroxide formation based on the Mn(III)-catalyzed aerobic oxidation
    • DOI 10.1016/j.tetlet.2003.11.054
    • Kumabe, R.; Nishino, H. Tetrahedron Lett. 2004, 45, 703. doi:10.1016/j.tetlet.2003.11.054 (Pubitemid 38032685)
    • (2004) Tetrahedron Letters , vol.45 , Issue.4 , pp. 703-706
    • Kumabe, R.1    Nishino, H.2
  • 310
    • 27144560022 scopus 로고    scopus 로고
    • Manganese(III)-based oxidation of 2,4-piperidinediones in the presence of alkenes
    • DOI 10.1016/j.tet.2005.09.029, PII S0040402005015978
    • Asahi, K.; Nishino, H. Tetrahedron 2005, 61, 11107. doi:10.1016/j.tet. 2005.09.029 (Pubitemid 41502889)
    • (2005) Tetrahedron , vol.61 , Issue.47 , pp. 11107-11124
    • Asahi, K.1    Nishino, H.2
  • 311
    • 38349063003 scopus 로고    scopus 로고
    • doi:10.1016/j.tet.2007.12.017
    • Asahi, K.; Nishino, H. Tetrahedron 2008, 64, 1620. doi:10.1016/j.tet. 2007.12.017
    • (2008) Tetrahedron , vol.64 , pp. 1620
    • Asahi, K.1    Nishino, H.2
  • 315
    • 0037128466 scopus 로고    scopus 로고
    • An efficient synthesis of bridged-bicyclic peroxides structurally related to antimalarial yingzhaosu A based on radical co-oxygenation of thiols and monoterpenes
    • DOI 10.1016/S0040-4020(02)00126-6, PII S0040402002001266
    • Korshin, E. E.; Hoos, R.; Szpilman, A. M.; Konstantinovski, L.; Posner, G. H.; Bachi, M. D. Tetrahedron 2002, 58, 2449. doi:10.1016/S0040-4020(02)00126- 6 (Pubitemid 34215054)
    • (2002) Tetrahedron , vol.58 , Issue.12 , pp. 2449-2469
    • Korshin, E.E.1    Hoos, R.2    Szpilman, A.M.3    Konstantinovski, L.4    Posner, G.H.5    Bachi, M.D.6
  • 319
    • 24944566770 scopus 로고    scopus 로고
    • Co-catalyzed autoxidation of alkene in the presence of silane. The effect of the structure of silanes on the efficiency of the reaction and on the product distribution
    • DOI 10.1016/j.tet.2005.08.025, PII S0040402005013803
    • Wu, J.-M.; Kunikawa, S.; Tokuyasu, T.; Masuyama, A.; Nojima, M.; Kim, H.-S.; Wataya, Y. Tetrahedron 2005, 61, 9961. doi:10.1016/j.tet.2005.08.025 (Pubitemid 41317472)
    • (2005) Tetrahedron , vol.61 , Issue.42 , pp. 9961-9968
    • Wu, J.-M.1    Kunikawa, S.2    Tokuyasu, T.3    Masuyama, A.4    Nojima, M.5    Kim, H.-S.6    Wataya, Y.7
  • 322
    • 0035829094 scopus 로고    scopus 로고
    • Facile construction of 6-carbomethoxymethyl-3-methoxy-1,2-dioxane, a core structure of spongean anti-malarial peroxides
    • DOI 10.1016/S0040-4039(01)01493-9, PII S0040403901014939
    • Murakami, N.; Kawanishi, M.; Itagaki, S.; Horii, T.; Kobayashi, M. Tetrahedron Lett. 2001, 42, 7281. doi:10.1016/S0040-4039(01)01493-9 (Pubitemid 32913236)
    • (2001) Tetrahedron Letters , vol.42 , Issue.41 , pp. 7281-7285
    • Murakami, N.1    Kawanishi, M.2    Itagaki, S.3    Horii, T.4    Kobayashi, M.5
  • 325
    • 22544479436 scopus 로고    scopus 로고
    • Synthesis of 1,6,7-trioxa-spiro[4.5]decanes
    • DOI 10.1016/j.tetlet.2005.06.110, PII S0040403905013638
    • Jin, H.-X.; Liu, H.-H.; Zhang, Q.; Wu, Y. Tetrahedron Lett. 2005, 46, 5767. doi:10.1016/j.tetlet.2005.06.110 (Pubitemid 41019185)
    • (2005) Tetrahedron Letters , vol.46 , Issue.34 , pp. 5767-5769
    • Jin, H.-X.1    Liu, H.-H.2    Zhang, Q.3    Wu, Y.4
  • 326
    • 33745584335 scopus 로고    scopus 로고
    • Design, synthesis and in vitro antimalarial activity of spiroperoxides
    • DOI 10.1016/j.tet.2006.05.065, PII S0040402006008581
    • Jin, H.-X.; Zhang, Q.; Kim, H.-S.; Wataya, Y.; Liu, H.-H.; Wu, Y. Tetrahedron 2006, 62, 7699. doi:10.1016/j.tet.2006.05.065 (Pubitemid 43994040)
    • (2006) Tetrahedron , vol.62 , Issue.33 , pp. 7699-7711
    • Jin, H.-X.1    Zhang, Q.2    Kim, H.-S.3    Wataya, Y.4    Liu, H.-H.5    Wu, Y.6
  • 327
    • 19544367275 scopus 로고    scopus 로고
    • On the susceptibility of organic peroxy bonds to hydride reduction
    • DOI 10.1021/jo050139y
    • Jin, H.-X.; Liu, H.-H.; Zhang, Q.; Wu, Y. J. Org. Chem. 2005, 70, 4240. doi:10.1021/jo050139y (Pubitemid 40734133)
    • (2005) Journal of Organic Chemistry , vol.70 , Issue.11 , pp. 4240-4247
    • Jin, H.-X.1    Liu, H.-H.2    Zhang, Q.3    Wu, Y.4
  • 329
    • 20544431536 scopus 로고    scopus 로고
    • Total synthesis of peroxyacarnoates A and D: Metal-mediated couplings as a convergent approach to polyunsaturated peroxides
    • DOI 10.1021/ol050291m
    • Xu, C.; Raible, J. M.; Dussault, P. H. Org. Lett. 2005, 7, 2509. doi:10.1021/ol050291m (Pubitemid 40847673)
    • (2005) Organic Letters , vol.7 , Issue.12 , pp. 2509-2511
    • Xu, C.1    Raible, J.M.2    Dussault, P.H.3
  • 331
    • 34548339251 scopus 로고    scopus 로고
    • doi:10.1002/cjoc.200790242
    • Zhang, Q.; Li, Y.; Wu, Y.-K. Chin. J. Chem. 2007, 25, 1304. doi:10.1002/cjoc.200790242
    • (2007) Chin. J. Chem. , vol.25 , pp. 1304
    • Zhang, Q.1    Li, Y.2    Wu, Y.-K.3
  • 333
    • 0034712306 scopus 로고    scopus 로고
    • Halonium ion-mediated reaction of unsaturated hydroperoxy acetals. Competition between the formation of cyclic peroxides and the migration of the methoxy (or hydroxy) group
    • DOI 10.1021/jo991499m
    • Tokuyasu, T.; Masuyama, A.; Nojima, M.; McCullough, K. J. J. Org. Chem. 2000, 65, 1069. doi:10.1021/jo991499m (Pubitemid 30117378)
    • (2000) Journal of Organic Chemistry , vol.65 , Issue.4 , pp. 1069-1075
    • Tokuyasu, T.1    Masuyama, A.2    Nojima, M.3    McCullough, K.J.4
  • 334
    • 0034701597 scopus 로고    scopus 로고
    • Synthesis and anti-malarial activity of yingzhaosu A analogues from unsaturated hydroperoxy acetals
    • DOI 10.1016/S0040-4039(00)00372-5, PII S0040403900003725
    • Tokuyasu, T.; Masuyama, A.; Nojima, M.; Kim, H.-S.; Wataya, Y. Tetrahedron Lett. 2000, 41, 3145. doi:10.1016/S0040-4039(00)00372-5 (Pubitemid 30256759)
    • (2000) Tetrahedron Letters , vol.41 , Issue.17 , pp. 3145-3148
    • Tokuyasu, T.1    Masuyama, A.2    Nojima, M.3    Kim, H.-S.4    Wataya, Y.5
  • 337
    • 15944384634 scopus 로고    scopus 로고
    • Lewis acid catalysed rearrangements of unsaturated bicyclic [2.2.n] endoperoxides in the presence of vinyl silanes; access to novel Fenozan BO-7 analogues
    • DOI 10.1016/j.tetlet.2005.03.022
    • O'Neill, P. M.; Rawe, S. L.; Storr, R. C.; Ward, S. A.; Posner, G. H. Tetrahedron Lett. 2005, 46, 3029. doi:10.1016/j.tetlet.2005.03.022 (Pubitemid 40445428)
    • (2005) Tetrahedron Letters , vol.46 , Issue.17 , pp. 3029-3032
    • O'Neill, P.M.1    Rawe, S.L.2    Storr, R.C.3    Ward, S.A.4    Posner, G.H.5
  • 338
    • 0035833052 scopus 로고    scopus 로고
    • Yingzhaosu A analogues: Synthesis by the ozonolysis of unsaturated hydroperoxides, structural analysis and determination of anti-malarial activity
    • DOI 10.1016/S0040-4020(01)00557-9, PII S0040402001005579
    • Tokuyasu, T.; Masuyama, A.; Nojima, M.; McCullough, K. J.; Kim, H.-S.; Wataya, Y. Tetrahedron 2001, 57, 5979. doi:10.1016/S0040-4020(01)00557-9 (Pubitemid 32607604)
    • (2001) Tetrahedron , vol.57 , Issue.28 , pp. 5979-5989
    • Tokuyasu, T.1    Masuyama, A.2    Nojima, M.3    McCullough, K.J.4    Kim, H.-S.5    Wataya, Y.6
  • 341
    • 0343526760 scopus 로고    scopus 로고
    • The [4 + 2] addition of singlet oxygen to thebaine: New access to highly functionalized morphine derivatives via opioid endoperoxides
    • DOI 10.1021/jo000288a
    • López, D.; Quiñoá, E.; Riguera, R. J. Org. Chem. 2000, 65, 4671. doi:10.1021/jo000288a (Pubitemid 30620578)
    • (2000) Journal of Organic Chemistry , vol.65 , Issue.15 , pp. 4671-4678
    • Lopez, D.1    Quinoa, E.2    Riguera, R.3
  • 342
    • 0035808873 scopus 로고    scopus 로고
    • Reaction of 4,7-dimethylbenzofurazan with singlet oxygen
    • DOI 10.1016/S0040-4039(00)02216-4, PII S0040403900022164
    • Takabatake, T.; Miyazawa, T.; Hasegawa, M.; Foote, C. S. Tetrahedron Lett. 2001, 42, 987. doi:10.1016/S0040-4039(00)02216-4 (Pubitemid 32149826)
    • (2001) Tetrahedron Letters , vol.42 , Issue.6 , pp. 987-989
    • Takabatake, T.1    Miyazawa, T.2    Hasegawa, M.3    Foote, C.S.4
  • 343
    • 0035959455 scopus 로고    scopus 로고
    • Rearrangement of unsaturated cyclic peroxides obtained by photooxygenation of 2,3-dimethylene-7-oxabenzonorbornene and 2,3-dimethylene-1,4-etheno-1,2,3,4-tetrahydronaphthalene
    • DOI 10.1016/S0040-4020(01)00702-5, PII S0040402001007025
    • Özen, R.; Kormali, F.; Balci, M.; Atasoy, B. Tetrahedron 2001, 57, 7529. doi:10.1016/S0040-4020(01)00702-5 (Pubitemid 32770036)
    • (2001) Tetrahedron , vol.57 , Issue.35 , pp. 7529-7535
    • Ozen, R.1    Kormali, F.2    Balci, M.3    Atasoy, B.4
  • 344
    • 0034801640 scopus 로고    scopus 로고
    • 10.1002 1099-0690 (200109) 2001:18〈3519::AID-EJOC3519〉3.0.C O;2-2
    • Dastan, A.; Saracoglu, N.; Balci, M. Eur. J. Org. Chem. 2001, 3519. doi:10.1002/1099-0690(200109)2001:18〈3519::AID-EJOC3519〉3.0.C O;2-2
    • (2001) Eur. J. Org. Chem. , vol.3519
    • Dastan, A.1    Saracoglu, N.2    Balci, M.3
  • 345
    • 18744364696 scopus 로고    scopus 로고
    • Chemistry of the benzotropone endoperoxides and their conversion into tropolone derivatives: Unusual endoperoxide rearrangements
    • DOI 10.1002/hlca.200590061
    • Güney, M.; Dastan, A.; Balci, M. Helv. Chim. Acta 2005, 88, 830. doi:10.1002/hlca.200590061 (Pubitemid 40675104)
    • (2005) Helvetica Chimica Acta , vol.88 , Issue.4 , pp. 830-838
    • Guney, M.1    Dastan, A.2    Balci, M.3
  • 346
    • 33646168563 scopus 로고    scopus 로고
    • doi:10.1016/j.tet.2006.02.026
    • Dastan, A.; Balci, M. Tetrahedron 2006, 62, 4003. doi:10.1016/j.tet.2006. 02.026
    • (2006) Tetrahedron , vol.62 , pp. 4003
    • Dastan, A.1    Balci, M.2
  • 347
    • 20044373094 scopus 로고    scopus 로고
    • Substituent effects of the cycloaddition reaction of 7-substituted 5H-benzocycloheptenes with singlet oxygen and the chemistry of the benzocycloheptene endoperoxides
    • DOI 10.1139/v05-046
    • Güney, M.; Ceylan, Z. C.; Dastan, A.; Balci, M. Can. J. Chem. 2005, 83, 227. doi:10.1139/v05-046 (Pubitemid 40768926)
    • (2005) Canadian Journal of Chemistry , vol.83 , Issue.3 , pp. 227-235
    • Guney, M.1    Ceylan, Z.C.2    Dastan, A.3    Balci, M.4
  • 348
    • 34249041979 scopus 로고    scopus 로고
    • 2+ catalyzes vitamin E-induced fragmentation of hydroperoxy and hydroxy endoperoxides that generates γ-hydroxy alkenals
    • DOI 10.1021/ja0689785
    • Gu, X.; Zhang, W.; Salomon, R. G. J. Am. Chem. Soc. 2007, 129, 6088. doi:10.1021/ja0689785 (Pubitemid 46786794)
    • (2007) Journal of the American Chemical Society , vol.129 , Issue.19 , pp. 6088-6089
    • Gu, X.1    Zhang, W.2    Salomon, R.G.3
  • 349
    • 23044500760 scopus 로고    scopus 로고
    • Total syntheses of four stereoisomers of 4α-hydroxy-1β, 7β- peroxy-10βH-guaia-5-ene
    • DOI 10.1021/ol0511023
    • Blay, G.; Garcia, B.; Molina, E.; Pedro, J. R. Org. Lett. 2005, 7, 3291. doi:10.1021/ol0511023 (Pubitemid 41059128)
    • (2005) Organic Letters , vol.7 , Issue.15 , pp. 3291-3294
    • Blay, G.1    Garcia, B.2    Molina, E.3    Pedro, J.R.4
  • 351
    • 23644457151 scopus 로고    scopus 로고
    • Synthesis of 2,3-Di- and 2,3,4-trisubstituted furans from 1,2-dioxines generated by an enyne-RCM/Diels-Alder reaction sequence
    • DOI 10.1021/jo050957q
    • Yang, Y.-K.; Choi, J.-H.; Tae, J. J. Org. Chem. 2005, 70, 6995. doi:10.1021/jo050957q (Pubitemid 41134409)
    • (2005) Journal of Organic Chemistry , vol.70 , Issue.17 , pp. 6995-6998
    • Yang, Y.-K.1    Choi, J.-H.2    Tae, J.3
  • 358
    • 0344666649 scopus 로고    scopus 로고
    • Hydroperoxide and Endoperoxide Lactones from Photooxygenation of 3-Alkylidenedihydrofuran-2,4-diones
    • DOI 10.1021/jo030270a
    • Schobert, R.; Stehle, R.; Milius, W. J. Org. Chem. 2003, 68, 9827. doi:10.1021/jo030270a (Pubitemid 37509898)
    • (2003) Journal of Organic Chemistry , vol.68 , Issue.25 , pp. 9827-9830
    • Schobert, R.1    Stehle, R.2    Milius, W.3
  • 359
    • 0035952966 scopus 로고    scopus 로고
    • Bicyclic peroxides in the G factors series: Synthesis and electrochemical studies
    • DOI 10.1016/S0040-4039(01)00199-X, PII S004040390100199X
    • Gavrilan, M.; André-Barrès, C.; Baltas, M.; Tzedakis, T.; Gorrichon, L. Tetrahedron Lett. 2001, 42, 2465. doi:10.1016/S0040-4039(01)00199- X (Pubitemid 32234325)
    • (2001) Tetrahedron Letters , vol.42 , Issue.13 , pp. 2465-2468
    • Gavrilan, M.1    Andre-Barres, C.2    Baltas, M.3    Tzedakis, T.4    Gorrichon, L.5
  • 361
    • 27744550853 scopus 로고    scopus 로고
    • Stable spiro-endoperoxides by sunlight-mediated photooxygenation of 1,2-O-alkylidene-5(E)-eno-5,6,8-trideoxy-α-D-xylo-oct-1,4-furano-7-uloses
    • DOI 10.1016/j.carres.2005.09.006, PII S0008621505004209
    • Çetin, F.; Yenil, N.; Yüceer, L. Carbohydr. Res. 2005, 340, 2583. doi:10.1016/j.carres.2005.09.006 (Pubitemid 41606758)
    • (2005) Carbohydrate Research , vol.340 , Issue.17 , pp. 2583-2589
    • Cetin, F.1    Yenil, N.2    Yuceer, L.3
  • 365
    • 33749037979 scopus 로고    scopus 로고
    • Osmium catalyzed dihydroxylation of 1,2-dioxines: A new entry for stereoselective sugar synthesis
    • DOI 10.1021/jo060949p
    • Robinson, T. V.; Taylor, D. K.; Tiekink, E. R. T. J. Org. Chem. 2006, 71, 7236. doi:10.1021/jo060949p (Pubitemid 44452901)
    • (2006) Journal of Organic Chemistry , vol.71 , Issue.19 , pp. 7236-7244
    • Robinson, T.V.1    Taylor, D.K.2    Tiekink, E.R.T.3
  • 369
    • 18844463439 scopus 로고    scopus 로고
    • Synthesis and chemistry of unusual bicyclic endoperoxides containing the pyridazine ring
    • DOI 10.1021/jo0345300
    • Özer, G.; Saraçoǧlu, N.; Balci, M. J. Org. Chem. 2003, 68, 7009. doi:10.1021/jo0345300 (Pubitemid 37071781)
    • (2003) Journal of Organic Chemistry , vol.68 , Issue.18 , pp. 7009-7015
    • Ozer, G.1    Saracoglu, N.2    Balci, M.3
  • 370
    • 0025027645 scopus 로고
    • Preparation of β-hydroxyhydroperoxides by photooxygenation of allylic alcohols and their elaboration into 1,2,4-trioxanes
    • DOI 10.1016/S0040-4039(00)97202-2
    • Singh, C. Tetrahedron Lett. 1990, 31, 6901. doi:10.1016/S0040-4039(00) 97202-2 (Pubitemid 20358459)
    • (1990) Tetrahedron Letters , vol.31 , Issue.47 , pp. 6901-6902
    • Singh, C.1
  • 372
    • 0141851824 scopus 로고    scopus 로고
    • Geraniol-derived 1,2,4-trioxanes with potent in-vivo antimalarial activity
    • DOI 10.1016/S0960-894X(03)00782-0
    • Singh, C.; Gupta, N.; Puri, S. K. Bioorg. Med. Chem. Lett. 2003, 13, 3447. doi:10.1016/S0960-894X(03)00782-0 (Pubitemid 37141405)
    • (2003) Bioorganic and Medicinal Chemistry Letters , vol.13 , Issue.20 , pp. 3447-3450
    • Singh, C.1    Gupta, N.2    Puri, S.K.3
  • 373
    • 0037025438 scopus 로고    scopus 로고
    • Photo-oxygenation of geraniol: Synthesis of a novel series of hydroxy-functionalized anti-malarial 1,2,4-trioxanes
    • DOI 10.1016/S0960-894X(02)00320-7, PII S0960894X02003207
    • Singh, C.; Gupta, N.; Puri, S. K. Bioorg. Med. Chem. Lett. 2002, 12, 1913. doi:10.1016/S0960-894X(02)00320-7 (Pubitemid 34756447)
    • (2002) Bioorganic and Medicinal Chemistry Letters , vol.12 , Issue.15 , pp. 1913-1916
    • Singh, C.1    Gupta, N.2    Puri, S.K.3
  • 375
    • 24344441636 scopus 로고    scopus 로고
    • New orally active spiro 1,2,4-trioxanes with high antimalarial potency
    • DOI 10.1016/j.bmcl.2005.07.013, PII S0960894X0500884X
    • Singh, C.; Malik, H.; Puri, S. K. Bioorg. Med. Chem. Lett. 2005, 15, 4484. doi:10.1016/j.bmcl.2005.07.013 (Pubitemid 41258172)
    • (2005) Bioorganic and Medicinal Chemistry Letters , vol.15 , Issue.20 , pp. 4484-4487
    • Singh, C.1    Malik, H.2    Puri, S.K.3
  • 376
    • 29344476145 scopus 로고    scopus 로고
    • Protection of the carbonyl group as 1,2,4-trioxane and its regeneration under basic conditions
    • DOI 10.1021/ol052378d
    • Singh, C.; Malik, H. Org. Lett. 2005, 7, 5673. doi:10.1021/ol052378d (Pubitemid 43010826)
    • (2005) Organic Letters , vol.7 , Issue.25 , pp. 5673-5676
    • Singh, C.1    Malik, H.2
  • 377
    • 1342321884 scopus 로고    scopus 로고
    • Synthesis and antimalarial activity of a new series of trioxaquines
    • DOI 10.1016/j.bmc.2003.11.021
    • Singh, C.; Malik, H.; Puri, S. K. Bioorg. Med. Chem. 2004, 12, 1177. doi:10.1016/j.bmc.2003.11.021 (Pubitemid 38251307)
    • (2004) Bioorganic and Medicinal Chemistry , vol.12 , Issue.5 , pp. 1177-1182
    • Singh, C.1    Malik, H.2    Puri, S.K.3
  • 378
    • 29544437054 scopus 로고    scopus 로고
    • 8-(1-Naphthalen-2-yl-vinyl)-6,7,10-trioxaspiro (4.5) decane, a new 1,2,4-trioxane effective against rodent and simian malaria
    • DOI 10.1016/j.bmcl.2005.10.044, PII S0960894X05013375
    • Singh, C.; Kanchan, R.; Srivastava, N. C.; Puri, S. K. Bioorg. Med. Chem. Lett. 2006, 16, 584. doi:10.1016/j.bmcl.2005.10.044 (Pubitemid 43014841)
    • (2006) Bioorganic and Medicinal Chemistry Letters , vol.16 , Issue.3 , pp. 584-586
    • Singh, C.1    Kanchan, R.2    Srivastava, D.3    Puri, S.K.4
  • 381
    • 4744374690 scopus 로고    scopus 로고
    • Synthesis of new 6-alkylvinyl/arylalkylvinyl substituted 1,2,4-trioxanes active against multidrug-resistant malaria in mice
    • DOI 10.1016/j.bmc.2004.08.005, PII S0968089604006078
    • Singh, C.; Gupta, N.; Puri, S. K. Bioorg. Med. Chem. 2004, 12, 5553. doi:10.1016/j.bmc.2004.08.005 (Pubitemid 39310506)
    • (2004) Bioorganic and Medicinal Chemistry , vol.12 , Issue.21 , pp. 5553-5562
    • Singh, C.1    Gupta, N.2    Puri, S.K.3
  • 382
    • 10044264584 scopus 로고    scopus 로고
    • Photooxygenation of 3-aryl-2-cyclohexenols: Synthesis of a new series of antimalarial 1,2,4-trioxanes
    • DOI 10.1016/j.tetlet.2004.11.078, PII S0040403904025432
    • Singh, C.; Gupta, N.; Puri, S. K. Tetrahedron Lett. 2005, 46, 205. doi:10.1016/j.tetlet.2004.11.078 (Pubitemid 39602602)
    • (2005) Tetrahedron Letters , vol.46 , Issue.2 , pp. 205-207
    • Singh, C.1    Gupta, N.2    Puri, S.K.3
  • 383
    • 6344263386 scopus 로고    scopus 로고
    • Synthesis and antimalarial activity of 6-cycloalkylvinyl substituted 1,2,4-trioxanes
    • DOI 10.1016/j.bmc.2004.08.042, PII S0968089604006662
    • Singh, C.; Srivastava, N. C.; Puri, S. K. Bioorg. Med. Chem. 2004, 12, 5745. doi:10.1016/j.bmc.2004.08.042 (Pubitemid 39388173)
    • (2004) Bioorganic and Medicinal Chemistry , vol.12 , Issue.22 , pp. 5745-5752
    • Singh, C.1    Srivastav, N.C.2    Puri, S.K.3
  • 385
    • 24944563423 scopus 로고    scopus 로고
    • A family of new 1,2,4-trioxanes by photooxygenation of allylic alcohols in sensitizer-doped polymers and secondary reactions
    • DOI 10.1055/s-2005-872103, T06105SS
    • Bartoschek, A.; El-Idreesy, T. T.; Griesbeck, A. G.; Höinck, L.-O.; Lex, J.; Miara, C.; Neudörfl, J. M. Synthesis 2005, 2433. doi:10.1055/s-2005-872103 (Pubitemid 41306182)
    • (2005) Synthesis , Issue.14 , pp. 2433-2444
    • Bartoschek, A.1    El-Idreesy, T.T.2    Griesbeck, A.G.3    Hoinck, L.-O.4    Lex, J.5    Miara, C.6    Neudorfl, J.M.7
  • 386
    • 33749343243 scopus 로고    scopus 로고
    • Singlet oxygen addition to chiral allylic alcohols and subsequent peroxyacetalization with β-naphthaldehyde: Synthesis of diastereomerically pure 3-β-naphthyl-substituted 1,2,4-trioxanes
    • DOI 10.1016/j.tet.2006.05.093, PII S0040402006013706, Organic Chemistry of Singlet Oxygen
    • Griesbeck, A. G.; El-Idreesy, T. T.; Lex, J. Tetrahedron 2006, 62, 10615. doi:10.1016/j.tet.2006.05.093 (Pubitemid 44488701)
    • (2006) Tetrahedron , vol.62 , Issue.46 , pp. 10615-10622
    • Griesbeck, A.G.1    El-Idreesy, T.T.2    Lex, J.3
  • 390
    • 33846926709 scopus 로고    scopus 로고
    • New adamantane-based spiro 1,2,4-trioxanes orally effective against rodent and simian malaria
    • DOI 10.1021/jm0610043
    • Singh, C.; Kanchan, R.; Sharma, U.; Puri, S. K. J. Med. Chem. 2007, 50, 521. doi:10.1021/jm0610043 (Pubitemid 46239786)
    • (2007) Journal of Medicinal Chemistry , vol.50 , Issue.3 , pp. 521-527
    • Singh, C.1    Kanchan, R.2    Sharma, U.3    Puri, S.K.4
  • 392
    • 67649380741 scopus 로고    scopus 로고
    • doi:10.1055/s-0029-1216740
    • Griesbeck, A. G.; Raabe, A. Synlett 2009, 1514. doi:10.1055/s-0029- 1216740
    • (2009) Synlett , vol.1514
    • Griesbeck, A.G.1    Raabe, A.2
  • 399
    • 0037463534 scopus 로고    scopus 로고
    • UV irradiation of arylidene-β-ionones in the presence of dioxygen: Regioselective formation of stable endoperoxides
    • DOI 10.1016/S0040-4039(03)00086-8, PII S0040403903000868
    • Singh, R.; Ishar, M. P. S. Tetrahedron Lett. 2003, 44, 1943. doi:10.1016/S0040-4039(03)00086-8 (Pubitemid 36192817)
    • (2003) Tetrahedron Letters , vol.44 , Issue.9 , pp. 1943-1945
    • Singh, R.1    Ishar, M.P.S.2
  • 400
    • 29744436121 scopus 로고    scopus 로고
    • Unique structural topology and reactivities of the ABD tricycle in phomactin A
    • DOI 10.1039/b511338e
    • Cole, K. P.; Hsung, R. P. Chem. Commun. 2005, 5784. doi:10.1039/b511338e (Pubitemid 43028754)
    • (2005) Chemical Communications , Issue.46 , pp. 5784-5786
    • Cole, K.P.1    Hsung, R.P.2
  • 403
    • 0035797060 scopus 로고    scopus 로고
    • Regioselective Mukaiyama hydroperoxysilylation of 2-alkyl- or 2-aryl-prop-2-en-1-ols: Application to a new synthesis of 1,2,4-trioxanes
    • DOI 10.1016/S0040-4039(01)00791-2, PII S0040403901007912
    • O'Neil, P. M.; Pugh, M.; Davies, J.; Ward, S. A.; Park, B. K. Tetrahedron Lett. 2001, 42, 4569. doi:10.1016/S0040-4039(01)00791-2 (Pubitemid 32537747)
    • (2001) Tetrahedron Letters , vol.42 , Issue.27 , pp. 4569-4571
    • O'Neill, P.M.1    Pugh, M.2    Davies, J.3    Ward, S.A.4    Park B.Kevin5
  • 404
  • 405
    • 20844440050 scopus 로고    scopus 로고
    • Dispiro-1,2,4-trioxane analogues of a prototype dispiro-1,2,4-trioxolane: Mechanistic comparators for artemisinin in the context of reaction pathways with iron(II)
    • DOI 10.1021/jo050385+
    • Tang, Y.; Dong, Y.; Wang, X.; Sriraghavan, K.; Wood, J. K.; Vennerstrom, J. L. J. Org. Chem. 2005, 70, 5103. doi:10.1021/jo050385+ (Pubitemid 40863912)
    • (2005) Journal of Organic Chemistry , vol.70 , Issue.13 , pp. 5103-5110
    • Tang, Y.1    Dong, Y.2    Wang, X.3    Sriraghavan, K.4    Wood, J.K.5    Vennerstrom, J.L.6
  • 409
    • 33750605426 scopus 로고    scopus 로고
    • A facile access to bridged 1,2,4-trioxanes
    • DOI 10.1016/j.tet.2006.09.061, PII S0040402006015286
    • Zhang, Q.; Jin, H.-X.; Wu, Y. Tetrahedron 2006, 62, 11627. doi:10.1016/j.tet.2006.09.061 (Pubitemid 44691877)
    • (2006) Tetrahedron , vol.62 , Issue.50 , pp. 11627-11634
    • Zhang, Q.1    Jin, H.-X.2    Wu, Y.3
  • 410
    • 34548238742 scopus 로고    scopus 로고
    • Further explorations on bridged 1,2,4-trioxanes
    • DOI 10.1016/j.tet.2007.07.090, PII S0040402007013397
    • Zhang, Q.; Wu, Y. Tetrahedron 2007, 63, 10189. doi:10.1016/j.tet.2007.07. 090 (Pubitemid 47320728)
    • (2007) Tetrahedron , vol.63 , Issue.41 , pp. 10189-10201
    • Zhang, Q.1    Wu, Y.2
  • 415
  • 419
    • 0041846741 scopus 로고    scopus 로고
    • 2/MTO/fluorous alcohol system
    • DOI 10.1016/S0040-4039(03)01472-2
    • Iskra, J.; Bonnet-Delpon, D.; Bégué, J. P. Tetrahedron Lett. 2003, 44, 6309. doi:10.1016/S0040-4039(03)01472-2 (Pubitemid 36897586)
    • (2003) Tetrahedron Letters , vol.44 , Issue.33 , pp. 6309-6312
    • Iskra, J.1    Bonnet-Delpon, D.2    Begue, J.-P.3
  • 421
    • 30744442274 scopus 로고    scopus 로고
    • Fluorinated alcohol directed formation of dispiro-1,2,4,5-tetraoxanes by hydrogen peroxide under acid conditions
    • DOI 10.1016/j.tet.2005.11.022, PII S0040402005020272
    • Žmitek, K.; Stavber, S.; Zupan, M.; Bonnet-Delpon, D.; Iskra, J. Tetrahedron 2006, 62, 1479. doi:10.1016/j.tet.2005.11.022 (Pubitemid 43099817)
    • (2006) Tetrahedron , vol.62 , Issue.7 , pp. 1479-1484
    • Zmitek, K.1    Stavber, S.2    Zupan, M.3    Bonnet-Delpon, D.4    Iskra, J.5
  • 422
    • 38949142635 scopus 로고    scopus 로고
    • Synthesis, thermal stability, antimalarial activity of symmetrically and asymmetrically substituted tetraoxanes
    • DOI 10.1016/j.bmcl.2007.12.069, PII S0960894X07015260
    • Atheaya, H.; Khan, S. I.; Mamgain, R.; Rawat, D. S. Bioorg. Med. Chem. Lett. 2008, 18, 1446. doi:10.1016/j.bmcl.2007.12.069 (Pubitemid 351226527)
    • (2008) Bioorganic and Medicinal Chemistry Letters , vol.18 , Issue.4 , pp. 1446-1449
    • Atheaya, H.1    Khan, S.I.2    Mamgain, R.3    Rawat, D.S.4
  • 423
  • 432
    • 0032515010 scopus 로고    scopus 로고
    • Dispiro-1,2,4,5-tetraoxanes via ozonolysis of cycloalkanone o-methyl oximes: A comparison with the peroxidation of cycloalkanones in acetonitrile- sulfuric acid media
    • DOI 10.1021/jo981261i
    • Dong, Y.; Vennerstrom, J. L. J. Org. Chem. 1998, 63, 8582. doi:10.1021/jo981261i (Pubitemid 28532924)
    • (1998) Journal of Organic Chemistry , vol.63 , Issue.23 , pp. 8582-8585
    • Dong, Y.1    Vennerstrom, J.L.2
  • 435
    • 0041880501 scopus 로고    scopus 로고
    • A new method for the synthesis of bishydroperoxides based on a reaction of ketals with hydrogen peroxide catalyzed by boron trifluoride complexes
    • DOI 10.1016/S0040-4039(03)01844-6
    • Terent'ev, A. O.; Kutkin, A. V.; Platonov, M. M.; Ogibin, Y. N.; Nikishin, G. I. Tetrahedron Lett. 2003, 44, 7359. doi:10.1016/S0040-4039(03) 01844-6 (Pubitemid 37088045)
    • (2003) Tetrahedron Letters , vol.44 , Issue.39 , pp. 7359-7363
    • Terent'ev, A.O.1    Kutkin, A.V.2    Platonov, M.M.3    Ogibin, Y.N.4    Nikishin, G.I.5


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