子结构搜索

C1CCOC1.O

COC[C@H]1O[C@@H](n2cnc3c(NC4CCCC4)ncnc32)[C@H](O)[C@@H]1O
Reaction #6761
N6-cyclopentyl-5′-O-methyladenosine
DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H]1O[C@@H](n2cnc3c(NCc4cccc(I)c4)ncnc32)[C@H](O)[C@@H]1O
Reaction #6762
N6-(3-iodobenzyl)-5′-O-methyladenosine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC[C@H]1O[C@@H](n2cnc3c(NC4CCCC4)ncnc32)[C@H](O)[C@@H]1O
Reaction #6765
N6-cyclopentyl-5′-O-ethyladenosine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC[C@H]1O[C@@H](n2cnc3c(NCc4cccc(I)c4)ncnc32)[C@H](O)[C@@H]1O
Reaction #6766
N6-(3-Iodobenzyl)-5′-O-Ethyladenosine
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)C2C3CCC(O3)C12
Reaction #8673
10-Oxa-4-azatricyclo[5.2.1.02,6] decane-3,5-dione
DOI: 10.6084/m9.figshare.5104873.v1
C1CC2OC1C1CNCC21
Reaction #8674
10-Oxa-4-azatricyclo[5.2.1.02,6]decane
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CC(=O)c1ccc(Br)cc1)C(=O)O
Reaction #9615
4-(4-bromophenyl)-2,2-dimethyl-4-oxobutanoic acid
收率 63.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC(F)(F)F)N[C@@]12C[C@H]1COC2=O
Reaction #10170
3,3,3-trifluoro-N-[(±)-trans-2-oxo-3-oxabicyclo[3.1.0]hex-1-yl]-propanamide
收率 45.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C2CCC(OC)O2)cc(OC)c1OC
Reaction #50766
2-(3,4,5-trimethoxyphenyl)-5 -methoxytetrahydrofuran
收率 27.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CC(=O)c1ccc(Br)cc1)C(=O)O
Reaction #59109
4-(4-bromophenyl)-2,2-dimethyl-4-oxobutanoic acid
收率 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1=CCC(/C=C/C2CCOC2=O)C1(C)C
Reaction #65057
(E)-3-[2-(2,2,3-trimethylcyclopent-3-en-yl)ethenyl]dihydro-2 (3H)-furanone
收率 42.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCC12CN(c3c(F)c(F)c4c(=O)c(C(=O)O)cn(C5CC5)c4c3F)CC1CCO2
Reaction #82161
7-(1-aminomethyl-2-oxa-7-aza-bicyclo[3.3.0]-oct-7-yl)-1-cyclopropyl-5,6,8-trifluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCC12CN(c3cc4c(cc3F)c(=O)c(C(=O)O)cn4[C@@H]3C[C@@H]3F)CC1CCO2
Reaction #82163
7-(1-aminomethyl-2-oxa-7-aza-bicyclo[3.3.0]oct-7-yl)-6-fluoro-1-(cis-2-fluorocyclopropyl)-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCC12CN(c3cc4c(cc3F)c(=O)c(C(=O)O)cn4-c3ccc(F)cc3F)CC1CCO2
Reaction #82165
7-(1-aminomethyl-2-oxa-7-azabicyclo[3.3.0]oct-7-yl)-1-(2,4-difluorophenyl)-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1C2C(=O)OC(=O)C12
Reaction #82988
2,4-dioxo-3-oxabicyclo[3.1.0]hexane-6-carboxylic acid
收率 83.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(=O)n(-c2ccc(NCCCC3CCCO3)c(F)c2)c(C)n1
Reaction #84499
title compound
收率 29.7%DOI: 10.6084/m9.figshare.5104873.v1
COCCCN[C@@H]1CCN(c2ccc(N3CCc4cc(OC[C@@H]5CCCO5)ccc4C3=O)cc2F)C1
Reaction #156690
2-{3-Fluoro-4-[(R)-3-(3-methoxy-propylamino)-pyrrolidin-1-yl]-phenyl}-6-[(S)-1-(tetrahydro-furan-2-yl)methoxy]-3,4-dihydro-2H-isoquinolin-1-one
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)COC(=O)C1O
Reaction #174953
DOI: 10.1039/C8SC04228D
CC(=O)OC1CC(n2cc(C#C[Si](C)(C)C)c3c(CCc4ccccc4)ncnc32)OC1CO[Si](C)(C)C(C)(C)C
Reaction #178143
DOI: 10.1039/C8SC04228D
c1cnc(Oc2ccc(Nc3nc4ccccc4s3)cc2)c(C2CCOC2)c1
Reaction #186050
DOI: 10.1039/C8SC04228D
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