部分構造検索

CCCCCCCCCCCCCCCCO

CCCCCCCCCCCCCCCCCCN(CCCCCCCCCCCCCCCCCC)C(=O)CCC(C)C1CCC2C3CCC4CC(OC(=O)ON5C(=O)CCC5=O)CCC4(C)C3CCC12C
Reaction #49205
Compound 83
収率 71.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)O[C@H]2CC[C@@]3(C)[C@@H](CC[C@@H]4[C@@H]3CC[C@]3(C)C(=O)CC[C@@H]43)C2)cc1
Reaction #92528
3β-tosyloxy-5α-androstan-17-one
収率 87.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](CC[C@@H](O)C(C)(C)O)[C@H]1CC[C@H]2C3=CC=C4C[C@@H](OC5CCCOC5)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #95326
(24R)-5,7-cholestadiene-3β,24,25-triol 3-tetrahydropyranyl ether
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(C(=O)O)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)OC)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172733
title compound
収率 99.1%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(N=C=O)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)OC)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172734
title compound
収率 86.4%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(C(=O)OCc3ccccc3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)OC)c(F)c6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172872
title compound
収率 89.2%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(C(=O)O)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)OC)c(F)c6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172873
title compound
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc([C@H]2CC[C@]3(C)[C@H]4CC[C@@H]5[C@H]6[C@H](C(C)C)CC[C@]6(C(=O)O)CC[C@@]5(C)[C@]4(C)CC[C@H]3C2(C)C)cc1
Reaction #172885
title compound
収率 82.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCOc1cc(OCCCCc2ccc3cc(OCc4ccccc4)c(OCc4ccccc4)cc3c2)cc(N(CC(=O)OC)CC(=O)OC)c1
Reaction #173808
DOI: 10.1039/C8SC04228D
CCOC(C)OC(C)(C)C(F)CCC(COS(=O)(=O)c1ccc(C)cc1)C1CCC2C3CC=C4CC(OC5CCCCO5)CC(OC5CCCCO5)C4(C)C3CCC12C
Reaction #182809
DOI: 10.1039/C8SC04228D
CC(C=O)C1CCC2C3C(OC(=O)N(C)C)C=C4CC(O)C5OC5C4(C)C3CCC12C
Reaction #193114
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCC(=O)OC(CCCCCCCCCCCCCCC)CC(=O)NCCC(=O)NC(C(=O)NC(CCC(=O)OCc1ccccc1)C(=O)OCc1ccccc1)C(C)O
Reaction #195293
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCCCOc1cc(OCCCOc2cccc([N+](=O)[O-])c2)cc(C(=O)N(CC(=O)OCC)CC(=O)OCC)c1
Reaction #202483
DOI: 10.1039/C8SC04228D
CC(=O)OC1CC2=CC=C3C4CCC(C(C)C5OCC(C)(C)CO5)C4(C)CCC3C2(C)C2OC12
Reaction #208184
DOI: 10.1039/C8SC04228D
COC(=O)OC1CC2=CC=C3C4CCC(C(C)CS(=O)c5ccccc5)C4(C)CCC3C2(C)C(OC(=O)OC)C1
Reaction #222886
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCOc1ccc(C=O)s1
Reaction #249510
DOI: 10.1039/C8SC04228D
CC12CCC(OCCNCCN3CCCC3)CC1CCC1C2CCC2(C)C(c3ccoc3)CCC12O
Reaction #255878
DOI: 10.1039/C8SC04228D
CN(CCC(=O)OC1CCC2(C)C(C1)C(=NO)CC1C3CCC(=O)C3(C)CCC12)C(=O)OCc1ccccc1
Reaction #261840
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCCCOc1ccc(C(=O)O)s1
Reaction #278743
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCCCON1C(C)(C)CC(CCCCNc2nc(NCCO)nc(NCCCCC3CC(C)(C)N(OCCCCCCCCCCCCCCCCCC)C(C)(C)C3)n2)CC1(C)C
Reaction #283360
DOI: 10.1039/C8SC04228D
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