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294440

CCCCCC1CCC(CCBr)CC1
Reaction #203072
DOI: 10.1039/C8SC04228D
CC12CCC3C(CC=C4CCCCC43C)C1CC(Br)C2=O
Reaction #210265
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #280010
DOI: 10.1039/C8SC04228D
CC1CCC2(C)C(=CCC3C4CC(O)C(=O)C4(C)CCC32)C1
Reaction #288865
DOI: 10.1039/C8SC04228D
CC(=O)SCC1=CCC2C3=CC=C4CC(O[Si](C)(C)C(C)(C)C)CC(O[Si](C)(C)C(C)(C)C)C4(C)C3CCC12C
Reaction #300794
DOI: 10.1039/C8SC04228D
C[C@]12CC[C@H]3[C@@H]([C@@H](O)C=C4C[C@@H](O)CC[C@@]43C)[C@@H]1C[C@@H](O)[C@@H]2O
Reaction #360879
3β,7β,16α,17β-tetrahydroxyandrost-5-ene
DOI: 10.6084/m9.figshare.5104873.v1
C#CC1(CCCCC)CCC(C2CCC(CCCCC)CC2)CC1
Reaction #467436
4-ethynyl-4,4′-dipentylbicyclohexyl
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCCCC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)[C@H](O)C[C@@H]12
Reaction #553691
light yellow prisms
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H](O)CC1=CC[C@@H]1[C@@H]2[C@@H](O)C[C@@]2(C)[C@H]1C[C@@H](Br)C21OCCO1
Reaction #739397
16α-bromo-17,17-ethylenedioxyandrost-5-ene-3β, 11β-diol
DOI: 10.6084/m9.figshare.5104873.v1
CC12CCC3C(CC=C4CC(O)CCC43C)C1CC(Br)C2=O
Reaction #781167
DOI: 10.1039/C8SC04228D
C[C@]12CC[C@H](O)CC1=CC[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1C=CC21OCCO1
Reaction #927365
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H](O)CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12.N[C@@H](C=O)[C@@H](O[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]1O)[C@@H](O)[C@H](O)CO
Reaction #935760
chondrosine dehydroepiandrosterone
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CC[C@@]2(C)C(=CC[C@@H]3[C@@H]2CC[C@]2(C)C(=O)[C@H](O)C[C@@H]32)C1
Reaction #948828
16α-hydroxy-3β-methylandrost-5-en-17-one
収率 65.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1ccc2c(c1)CC[C@@H]1[C@@H]2C(CCCCCCl)C[C@]2(C)C(=O)C(Br)C[C@@H]12
Reaction #1054905
3-acetoxy-16-bromo-11-(5-chloropentyl)-estra-1,3,5(10)-trien-17-one
収率 228.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC(CCCCCCl)[C@@H]3c4ccc(O)cc4CC[C@H]3[C@@H]1CC(O)C2=O
Reaction #1054906
11-(5-chloropentyl)-3,16-dihydroxy-estra-1,3,5(10)-trien-17-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)SCC1=CC[C@H]2C3=CC=C4C[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@]4(C)[C@H]3CC[C@]12C
Reaction #1102149
titled compound
収率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CN(CCC(=O)OC(C)(C)C)c2nc(C3CCC4(CCCCC4)CC3)cs2)s1
Reaction #1132248
3-[(5-methyl-thiophen-2-ylmethyl)-(4-spiro[5.5]undec-3-yl-thiazol-2-yl)-amino]-propionic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(-c2ccccc2)cc(F)c1OC(F)(F)F
Reaction #1167768
3',5'-difluoro-4'-trifluoromethoxybiphenyl
収率 90.1%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCCCC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)[C@H](O)C[C@@H]12
Reaction #1286336
light yellow prisms
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CC[C@@]2(C)C(=CC[C@@H]3[C@@H]2CC[C@]2(C)C(=O)[C@H](O)C[C@@H]32)C1
Reaction #1286345
16α-hydroxy-3β-methylandrost-5-en-17-one
収率 65.2%DOI: 10.6084/m9.figshare.5104873.v1
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