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327492

CCCCOC1=C(SCCCCCC(=O)O)[C@@H](/C=C/[C@@H](O)C[C@@H](C)CCCC)[C@H](O)C1
Reaction #3122
(11R,12S,13E,15S,17S)-9-butyloxy-11,15-dihydroxy-17,20-dimethyl-7-thiaprosta-8,13-dienoic acid
수율 14.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC[C@@H](C)C[C@H](O)/C=C/[C@@H]1C(SCCCCCC(=O)OC)=C(OC(=O)C(C)C)C[C@H]1O
Reaction #3124
methyl(11R,12S,13E,15S,17R)-9-isobutyryloxy-11,15-dihydroxy-17,20-dimethyl-7-thiaprosta-8,13-dienoate
수율 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCSC1=C(OC(=O)CCC)C[C@@H](O)[C@@H]1/C=C/[C@@H](O)CCCCC
Reaction #3129
(11R,12S,13E,15S)-9-butyryloxy-11,15-dihydroxy-7-thiaprosta-8,13-diene
수율 35.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@H](O)/C=C/[C@@H]1C(SCCCCCC(=O)OC)=C(OC(=O)[C@H](Cc2ccccc2)NC(=O)OCc2ccccc2)C[C@H]1O
Reaction #3131
methyl(11R,12S,13E,15S)-9-(N-benzyloxycarbonylphenylalanyloxy)-11,15-dihydroxy-7-thiaprosta-8,13-dienoate
수율 51.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@H](O)/C=C/[C@@H]1C(SCCCCCC(N)=O)=C(OC(=O)CCC)C[C@H]1O
Reaction #3134
(11R,12S,13E,15S)-9-butyryloxy-11,15-dihydroxy-7-thiaprosta-8,13-dienamide
수율 91.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(CC)OC1CC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CC(O)C2C)C(OC)CC3C)CCC1O
Reaction #6397
title compounds
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(O)(/C=C/[C@H]1CCC(=O)N1CCSCCCC(=O)O)CCCCC
Reaction #51254
alcohol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)=CCCC(O)C=C[C@H]1CCC(=O)[C@@H]1CCCCCCC(=O)O
Reaction #55566
9-keto-15-hydroxy-19-methyl-prosta-13,18-dienoic acid
수율 91.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@H](O)CC[C@@H]1[C@H]2Cc3cccc(OCC(=O)O)c3C[C@H]2C[C@H]1O
Reaction #67896
titled compound
수율 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@H](O)/C=C/[C@@H]1[C@@H](C/C=C\CCCC(=O)N(C)S(C)(=O)=O)[C@@H](O)C[C@H]1O
Reaction #77801
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)O[C@H]1CC[C@@]2(C)C(=C[C@H](O)[C@H]3[C@@H]4[C@@H]5C[C@@H]5C(=O)[C@@]4(C)CC[C@@H]32)C1
Reaction #93687
3β-(tert.-butyldimethylsilyloxy)-7β-hydroxy-15β,16β-methylene-5-androsten-17-one
수율 78.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CSCCCCC1=CC(O)CC1=O
Reaction #94690
compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCCCCC1=CC(O)CC1=O
Reaction #95256
2-(6-carboxyhexyl)-4-hydroxy-cyclopent-2-en-1-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(OC2CCCCO2)C=C1CCCCCC(C(=O)O)C1CCCCO1
Reaction #95257
4-tetrahydropyranyloxy-2-(6-tetrahydropyranylcarboxyhexyl)cyclopent-2-en-1-one
DOI: 10.6084/m9.figshare.5104873.v1
CCO[PH](=O)CCCCC1=CC(N)CC1
Reaction #174282
DOI: 10.1039/C8SC04228D
CCOC(C)OC1CCC(C)(OC)C(OC(C)=O)C=CC(C)C(C(C)=CC=CC(C)(CC2OC2C(C)C(CC)OC(C)OCC)OC(C)OCC)OC(=O)C1
Reaction #185552
DOI: 10.1039/C8SC04228D
CC1(C2=CCCCC2)OC(C(=O)O)=CC1=O
Reaction #196701
DOI: 10.1039/C8SC04228D
CCCCC[C@H](O)/C=C/[C@H]1[C@H](O)CC(=O)[C@@H]1C/C=C\CCCCOC(=O)NC
Reaction #214758
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)CCCC=CCC1C(O)CC(OC(=O)OCCCCI)C1C=CC(O)CCc1ccccc1
Reaction #229911
DOI: 10.1039/C8SC04228D
O=C(O)CCCCCCC1=CC(O)CC1=O
Reaction #238893
DOI: 10.1039/C8SC04228D
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