Spectra for:
I. S. Marcos, A. B. Pedrero, M. J. Sexmero, D. Diez, P. Basabe, N. García, R. F. Moro, H. B. Broughton, F. Mollinedo, J. G. Urones
Compound 1 18R-ACETOXY-20-HYDROXY-2,10,19(21)-CLADOCORATRIEN-22(20)-OLIDE;MAJOR-ISOMER
Compound 2 18R,20-Dihydroxy-2,10,19(21)-cladocoratrien-22(20)-olide;major-isomer
Compound 4 20,22-EPOXY-2,10,19,21-CLADOCORATETRAEN-18R-OL
Compound 5 18-ACETOXY-18A-HOMO-13,14,15,16-TETRANOR-1(10)-ENT-HALIMEN-12-AL
Compound 6 18A-HOMO-15-NOR-1(10)-ENT-HALIMEN-13,18-DIOL
Compound 7 METHYL-15-METHOXY-1(10),13E-ENT-HALIMADIEN-18-OATE
Compound 8 15-Methoxy-1(10),13E-ent-halimadien-18-ol
Compound 9 15-METHOXY-1(10),13E-ENT-HALIMADIEN-18-AL
Compound 10 15-METHOXY-18-TOSYLOXY-1(10),13E-ENT-HALIMADIENE
Compound 11 15-METHOXY-1(10),13E-ENT-HALIMADIEN-18-OIC-ACID
Compound 12 15-METHOXY-1(10),13E-ENT-HALIMADIEN-18-YL-CHLORIDE
Compound 13 (Z)-1-[(1S,5S,6R,8aS)-5-[(E)-5-methoxy-3-methylpent-3-enyl]-1,5,6-trimethyl-2,3,6,7,8,8a-hexahydronaphthalen-1-yl]-2-diazonioethenolate
![(Z)-1-[(1S,5S,6R,8aS)-5-[(E)-5-methoxy-3-methylpent-3-enyl]-1,5,6-trimethyl-2,3,6,7,8,8a-hexahydronaphthalen-1-yl]-2-diazonioethenolate](/api/compound/ITF40FUxXbZ.png?h=300&w=458 "(Z)-1-[(1S,5S,6R,8aS)-5-[(E)-5-methoxy-3-methylpent-3-enyl]-1,5,6-trimethyl-2,3,6,7,8,8a-hexahydronaphthalen-1-yl]-2-diazonioethenolate")
Compound 14 METHYL-15-METHOXY-18A-HOMO-1(10),13E-ENT-HALIMADIEN-18-OATE
Compound 15 ETHYL-15-METHOXY-18A-HOMO-1(10),13E-ENT-HALIMADIEN-18-OATE
Compound 16 15-METHOXY-18A-HOMO-1(10),13E-ENT-HALIMADIEN-18-OL
Compound 17 18A-HOMO-1(10),13E,18A(18)Z-ENT-HALIMATRIEN-15,18-DIOL-DIMETHYLETER
Compound 18 18A-HOMO-1(10),13E,18A(18)E-ENT-HALIMATRIEN-15,18-DIOL-DIMETHYLETER
Compound 19 15-METHOXY-18A-HOMO-1(10),13E-ENT-HALIMADIEN-18-AL
Compound 20 15-METHOXY-18A-HOMO-1,18-CYCLO-5(10),13E-ENT-HALIMADIEN-18S-OL
Compound 21 15-METHOXY-18A-HOMO-1,18-CYCLO-5(10),13E-ENT-HALIMADIEN-18R-OL
Compound 23 18-HYDROXY-18A-HOMO-14,15-DINOR-1(10)-ENT-HALIMEN-13-ONE
Compound 24 15-METHOXY-18-TOSYL-18A-HOMO-1(10),13E-ENT-HALIMADIENE
Compound 25 15-METHOXY-18-IODO-18A-HOMO-1(10),13E-ENT-HALIMADIENE
Compound 26 22-METHOXY-2,10,19(21)E-CLADOCORATRIEN
Compound 27 1(10),13E-ENT-HALIMADIEN-15,18-DIOL
Compound 28 18-HYDROXY-14,15-DINOR-1(10)-ENT-HALIMEN-13-ONE
Compound 29 15-NOR-1(10)-ENT-HALIMEN-13,18-DIOL
Compound 30 18A-HOMO-15-NOR-13-HYDROXY-1(10)-ENT-HALIMEN-18-AL
Compound 31 18-METHOXY-18A-HOMO-15-NOR-1(10),18A(18)Z-ENT-HALIMADIEN-13-OL
Compound 33 13-HYDROXY-18A-HOMO-15-NOR-1(10)-ENT-HALIMEN-18-AL
Compound 34 18A-HOMO-15-NOR-1,18-CYCLO-5(10)-ENT-HALIMEN-13,18R-DIOL
Compound 35 18A-HOMO-15-NOR-1,18-CYCLO-5(10)-ENT-HALIMEN-13-OL
Compound 37 18-ACETOXY-18A-HOMO-15-NOR-1(10)-ENT-HALIMEN-13-OL
Compound 39 PKZMBUXJGUSHTH-YKWDRNOUSA-N
Compound 40 18-ACETOXY-13-CHLORO-18A-HOMO-15-NOR-1(10)-ENT-HALIMENE
Compound 43 18-ACETOXY-18A-HOMO-14,15-DINOR-1(10)-ENT-HALIMEN-13-ONE
Compound 44 15,16-EPOXY-18A-HOMO-1(10),13(16),14-ENT-HALIMATRIEN-12R,18-DIOL
Compound 44 15,16-EPOXY-18A-HOMO-1(10),13(16),14-ENT-HALIMATRIEN-12S,18-DIOL
Compound 46 15,16-EPOXY-18A-HOMO-18-TOSYL-1(10),13(16),14-ENT-HALIMATRIEN-12S,18-DIOL
Compound 47 15,16-EPOXY-18A-HOMO-18-TOSYL-1(10),13(16),14-ENT-HALIMATRIEN-12R,18-DIOL
Compound 49 18-IODO-15,16-EPOXY-18A-HOMO-1(10),13(16),14-ENT-HALIMATRIEN-12R-OL
Compound 50 20,22-EPOXY-2,10,19,21-CLADOCORATETRAEN-18S-OL
Compound 51 20,22-EPOXY-2,10,19,21-CLADOCORATETRAEN-18-ONE
Compound 52 AOTYANQFKUPFBR-FTDWFBCZSA-N
Compound 53 18R-HYDROXY-2,10,19(21)-CLADOCORATRIEN-22(20)-OLIDE
Compound 54 XTLKVXIDQXFPPS-YIYLITLGSA-N
Compound 55 18S,20-DIHYDROXY-2,10,19(21)-CLADOCORATRIEN-22(20)-OLIDE;MAJOR-ISOMER
Compound 56 AOTYANQFKUPFBR-BFDHNVDPSA-N
Compound 57 18S-ACETOXY-20-HYDROXY-2,10,19(21)-CLADOCORATRIEN-22(20)-OLIDE;MAJOR-ISOMER
Compound 59 18S-HYDROXY-2,10,19(21)-CLADOCORATRIEN-22(20)-OLIDE
Compound 60 18S-ACETOXY-2,10,19(21)-CLADOCORATRIEN-22(20)-OLIDE
Citation
| Citation | J.ORG.CHEM.,68,7496(2003) |
|---|---|
| Journal | The Journal of Organic Chemistry |
| Issue | 19 |
| Volume | 68 |
| Page(s) | 7496-7504 |
| Year | 2003 |
| Author(s) | I. S. Marcos, A. B. Pedrero, M. J. Sexmero, D. Diez, P. Basabe, N. García, R. F. Moro, H. B. Broughton, F. Mollinedo, J. G. Urones |
| Publisher | American Chemical Society (ACS) |
| DOI | 10.1021/jo034663l |