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CCCCCCC.CCOC(=O)C

CC(=O)O[C@H]1CC[C@@]2(C)C(=CC[C@H]3[C@@H]4CC[C@H]([C@H](C)CCC(=O)Cl)[C@@]4(C)CC[C@@H]32)C1
Reaction #3185
3β-acetoxy-5-cholenic acid chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC(=O)[C@@]1(O[Si](C)(C)C)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O[Si](C)(C)C)C[C@@]21C
Reaction #42650
title compound
収率 103.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCC(=O)[C@@]1(O)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O[Si](C)(C)C)C[C@@]21C
Reaction #42651
title compound
収率 73.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCc1cccc(OCC)c1CO
Reaction #52054
2-ethoxy-6-pentadecyl-benzyl alcohol
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(=O)O[C@]1(C(=O)C(O)OC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)C)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@@]21C
Reaction #81347
(2S)-2-((1,1-dimethylethoxycarbonyl)-amino)-3-methyl-butyric acid [11β,21-dihydroxy-3,20-dioxo-9-fluoro-16β-methyl-17-valeroyloxy-pregna -1,4-dien-21-yl] ester
収率 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(=O)OCC(=O)O[C@H]1[C@@H](CC)C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@@]21C
Reaction #92988
above-identified compound
収率 77.5%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)CCC(C)C
Reaction #92989
above-identified compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)CCCC(=O)O
Reaction #92999
above-identified compound
収率 56.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(C)C(=O)OCC(=O)O[C@H]1[C@@H](CC)C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@@]21C
Reaction #93002
above-identified compound
収率 19.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(=O)OCC(=O)O[C@H]1[C@@H](CC)C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@@]21C
Reaction #93005
above-identified compound
収率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)C1CCCCC1
Reaction #93007
above-identified compound
収率 88.2%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H]1C[C@H]2[C@@H]3CCC4=CC(=O)CC[C@@H]4[C@H]3CC[C@]2(C)[C@H]1OC(=O)COC(=O)CCC1CCCCC1
Reaction #93008
above-identified compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCCC(C)C1CCC2C3CC=C4CC(OC(=O)CCC(=O)O)CCC4(C)C3CCC12C
Reaction #182766
DOI: 10.1039/C8SC04228D
CC(C)CCCC(C)C1CCC2(C#N)C3C=CC4C(C)(C)C(OC(=O)c5ccccc5)CCC4(C)C3CCC12C
Reaction #183662
DOI: 10.1039/C8SC04228D
COC(=O)C1(OC(=O)c2ccc(O)o2)C(C)CC2C3CC(F)C4=CC(=O)C=CC4(C)C34OC4CC21C
Reaction #185648
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cc(C2=C(c3cc(C(F)(F)F)ccc3OCc3ccccc3)CCC2)cc(N2CCCC2=O)c1
Reaction #185786
DOI: 10.1039/C8SC04228D
CC(C)CC12CCC3C4CCC(=O)C=C4CCC3C1CCC2OC(=O)CCc1ccccc1
Reaction #187524
DOI: 10.1039/C8SC04228D
CC(C)OC(=O)c1ccc2c(c1)CCC1C2=NN(c2ccc(C#N)c(Cl)c2)C1C1CCCC1
Reaction #200804
DOI: 10.1039/C8SC04228D
Cc1nc2ccccc2n1C1CC2CCC(C1)N2CCC1(c2cccc(F)c2)CCN(C(C)C(=O)OCc2ccccc2)CC1
Reaction #203588
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCC(O)C1=CC(=O)OC1OC
Reaction #205927
DOI: 10.1039/C8SC04228D
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