子结构搜索

CCCCCCCI

C=CCOCCCCCCCCCCOc1ccc(C(=O)O)cc1
Reaction #5259
4-(10-allyloxydecyloxy)benzoic acid
收率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CCCCCCCI)C(=O)OC(C)(C)C
Reaction #5510
t-butyl methyl 7-iodoheptylmalonate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC12Cc3cc(OCOC)ccc3C1=C(C)C(=O)C(I)C2
Reaction #7960
(2SR,9aRS)-9a-butyl-2-iodo-7-methoxymethoxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC12Cc3cc(O)ccc3C1=C(C)C(=O)C(I)C2
Reaction #7961
(2SR,9aRS)-9a-butyl-7-hydroxy-2-iodo-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)Nc1cccc2c(C3(CCCI)CCc4cc(F)ccc43)c[nH]c12
Reaction #41996
title compound
收率 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CNCCCC1(c2c[nH]c3c(NS(C)(=O)=O)cccc23)CCc2cc(F)ccc21
Reaction #41997
title compound
收率 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)Nc1cccc2c(C3(CCCN4CCOCC4)CCc4cc(F)ccc43)c[nH]c12
Reaction #41998
title compound
收率 83.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2nc(NC(=O)C(CC3CCC(F)(F)CC3)c3ccc4c(c3)Nc3ccccc3S4(=O)=O)sc2n1
Reaction #43276
3-(4,4-difluorocyclohexyl)-2-(5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-N-(5-methoxythiazolo[5,4-b]pyridin-2-yl)propionamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccn(Cc2ccccc2)n1)C(CC1CCC(F)(F)CC1)c1ccc2c(c1)Nc1ccccc1S2(=O)=O
Reaction #43277
N-(1-benzyl-1H-pyrazol-3-yl)-3-(4,4-difluorocyclohexyl)-2-(5,5-dioxo-5,10-dihydrophenothiazin-2-yl)propionamide
DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc(NC(=O)C(CC2CCC(F)(F)CC2)c2ccc3c(c2)Nc2ccccc2S3(=O)=O)n1
Reaction #43278
3-(4,4-difluorocyclohexyl)-2-(5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-N-(1-methyl-1H-pyrazol-3-yl)propionamide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(CN2CCC(O)(CNC(=O)OC(C)(C)C)CC2)CCCCC1
Reaction #44875
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CCCCCCCI)C(=O)OC(C)(C)C
Reaction #50265
t-butyl methyl 7-iodoheptylmalonate
DOI: 10.6084/m9.figshare.5104873.v1
ICCCCCCCCc1ccccc1
Reaction #50708
8-phenyloctyl iodide
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc(C#N)c1CCCCCCCCCc1ccccc1
Reaction #50709
2-(9-phenylnonyl)-1,3-benzenedicarbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(O)OCCOCC=CC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F
Reaction #66011
2-(4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundec-2-enyloxy)ethyl hydrogen sulfate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC[C@@H](CC[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)CC(=O)[C@@H]1Cc1cccc(OCc2ccccc2)c1)O[Si](C)(C)C(C)(C)C
Reaction #67887
(2R,3R,4R)-2-(3-(benzyloxy)benzyl)-4-tert-butyldimethylsilyoxy-3-((S)-3-tert-butyldimethylsilyoxyoctyl)cyclopentanone
DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(I)C(=O)C2C3CCC(O3)C12
Reaction #69962
4-Iodo-5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
收率 84.6%DOI: 10.6084/m9.figshare.5104873.v1
COC1=C(c2cnc(Cl)cc2C)C(=O)C2C3CCC(O3)C12
Reaction #69963
4-(6-chloro-4-methyl-pyridin-3-yl)-5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one
收率 64.9%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(c3cccnc3)=CC[C@@H]12
Reaction #81467
17-(3-Pyridyl)androsta-5,16-dien-3β-ol
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F
Reaction #81697
C8F17H
收率 93.8%DOI: 10.6084/m9.figshare.5104873.v1
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