Spectra for:
Edelmiro Moman, Daniel Nicoletti, Antonio Mouriño
Compound (E)-1G ETHYL-(22-E)-DE-A,B-18,22-CYCLO-8-HYDROXYCHOL-22-EN-24-ATE
Compound (Z)-1G ETHYL-(22-Z)-DE-A,B-18,22-CYCLO-8-HYDROXYCHOL-22-EN-24-ATE
Compound 1A ETHYL-(22-R)-DE-A,B-18,22-CYCLO-8-HYDROXYCHOLAN-24-ATE
Compound 1C (22-R)-DE-A,B-18,22-CYCLO-8-HYDROXY-24-NORCHOLAN-23-NITRILE
Compound 1D (22-S)-DE-A,B-18,22-CYCLO-8-HYDROXY-23-(4-NITROPHENYLSULFENYL)-24-NORCHOLAN-23-NITRILE;EPIMER-A
Compound 1E (22-R)-DE-A,B-18,22-CYCLO-8-HYDROXY-24-NORCHOLAN-23-PHENYLSULFONE
Compound 2A ETHYL-(18-S,22-R)-DE-A,B-18,22-CYCLO-8,18-EPOXYCHOLAN-24-ATE
Compound 3A ETHYL-(22-E)-DE-A,B-8-HYDROXYCHOL-22-EN-24-ATE
Compound 3B ETHYL-(22-E)-DE-A,B-8-(4-NITROPHENYLSULFENYL)-OXYCHOL-22-EN-24-ATE
Compound 3C (22-E)-DE-A,B-8-(4-NITROPHENYLSULFENYL)-OXY-24-NORCHOL-22-ENE-23-NITRILE
Compound 3D (22-E)-DE-A,B-8-(4-NITROPHENYLSULFENYL)-OXY-24-NORCHOL-22-ENE-23-PHENYLSULFONE
Compound 3E ETHYL-DE-A,B-8-(4-NITROPHENYLSULFENYL)-OXYCHOL-22-YN-24-ATE
Compound 4A (E,4R)-4-[(1R,3aR,7aR)-4-keto-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-1-yl]pent-2-enoic acid ethyl ester
![(E,4R)-4-[(1R,3aR,7aR)-4-keto-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-1-yl]pent-2-enoic acid ethyl ester](/api/compound/60gpWodMGnV.png?h=300&w=458 "(E,4R)-4-[(1R,3aR,7aR)-4-keto-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-1-yl]pent-2-enoic acid ethyl ester")
Compound 4B GEHRDQZTDGQOEA-RCYPQCIBSA-N
Compound 4C WROPGQMZSVIGSH-NWHADJPVSA-N
Compound 4D (4S)-4-[(1R,3aR,7aR)-4-keto-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-1-yl]pent-2-ynoic acid ethyl ester
![(4S)-4-[(1R,3aR,7aR)-4-keto-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-1-yl]pent-2-ynoic acid ethyl ester](/api/compound/KOqimmhQHzi.png?h=300&w=458 "(4S)-4-[(1R,3aR,7aR)-4-keto-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-1-yl]pent-2-ynoic acid ethyl ester")
Compound 6 DE-A,B-23,24-DINOR-8-HYDROXYCHOLAN-22-AL
Compound 7 8-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-DE-A,B-23,24-DINORCHOLAN-22-AL
![8-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-DE-A,B-23,24-DINORCHOLAN-22-AL](/api/compound/FmLn3q2Qgx6.png?h=300&w=458 "8-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-DE-A,B-23,24-DINORCHOLAN-22-AL")
Compound 8 (22-E)-DE-A,B-8-HYDROXY-24-NORCHOL-22-ENE-23-NITRILE
Compound 9 (22-E)-DE-A,B-8-HYDROXY-24-NORCHOL-22-ENE-23-PHENYLSULFONE
Compound 10 ETHYL-DE-A,B-8-HYDROXYCHOL-22-YN-24-ATE
Compound 11 ETHYL-(22-R)-DE-A,B-18,22-CYCLO-8-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-CHOLAN-24-ATE
![ETHYL-(22-R)-DE-A,B-18,22-CYCLO-8-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-CHOLAN-24-ATE](/api/compound/2LgeIcfjFff.png?h=300&w=458 "ETHYL-(22-R)-DE-A,B-18,22-CYCLO-8-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-CHOLAN-24-ATE")
Compound 12 8-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-DE-A,B-23,24-DINORCHOLAN-22-OL
![8-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-DE-A,B-23,24-DINORCHOLAN-22-OL](/api/compound/4YQMSSV3i8H.png?h=300&w=458 "8-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-DE-A,B-23,24-DINORCHOLAN-22-OL")
Compound 13 ETHYL-(22-E)-DE-A,B-8-(TERT.-BUTYLDIMETHYLSILYL)-OXYCHOL-22-EN-24-ATE
Compound 14 (22-E)-DE-A,B-8-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-24-NORCHOL-22-ENE-23-NITRILE
![(22-E)-DE-A,B-8-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-24-NORCHOL-22-ENE-23-NITRILE](/api/compound/DkNhGpD5U5W.png?h=300&w=458 "(22-E)-DE-A,B-8-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-24-NORCHOL-22-ENE-23-NITRILE")
Compound 15 (22-E)-DE-A,B-8-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-24-NORCHOL-22-ENE-23-PHENYLSULFONE
![(22-E)-DE-A,B-8-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-24-NORCHOL-22-ENE-23-PHENYLSULFONE](/api/compound/FjTBdxJAJwe.png?h=300&w=458 "(22-E)-DE-A,B-8-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-24-NORCHOL-22-ENE-23-PHENYLSULFONE")
Compound 16 ETHYL-DE-A,B-8-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-CHOL-22-YN-24-ATE
![ETHYL-DE-A,B-8-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-CHOL-22-YN-24-ATE](/api/compound/G3dGxu67aV1.png?h=300&w=458 "ETHYL-DE-A,B-8-[(TERT.-BUTYLDIMETHYLSILYL)-OXY]-CHOL-22-YN-24-ATE")
Citation
| Citation | ORG.LETTERS,8,1249(2006) |
|---|---|
| Journal | Organic Letters |
| Issue | 6 |
| Volume | 8 |
| Page(s) | 1249-1251 |
| Year | 2006 |
| Author(s) | Edelmiro Moman, Daniel Nicoletti, Antonio Mouriño |
| Publisher | American Chemical Society (ACS) |
| DOI | 10.1021/ol060231w |