部分構造検索

898060

C=CCSCC1=CC(C)(C)Nc2ccc(-c3ccc(OC)c(OC)c3)cc21
Reaction #54087
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccc3c(c2)C(CSCCc2ccccc2)=CC(C)(C)N3)cc1OC
Reaction #54088
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(B2OC(C)(C)C(C)(C)O2)ccc1OCc1cc2ccccc2o1
Reaction #57739
2-[2-methoxy-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenoxymethyl]-benzofuran
収率 29.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc(B(O)O)ccc1OCC(=O)O
Reaction #59030
title compound
収率 64.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cccc(-c3cccc(C(F)(F)F)n3)c2)ccc1OCc1ccccc1
Reaction #70917
2-(4′-(benzyloxy)-3′-methoxybiphenyl-3-yl)-6-(trifluoromethyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #77556
prisms
収率 71.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #77580
oil
収率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cc3c4c(c2)C2CCN(C(=O)OC(C)(C)C)CCC2N4CCO3)cc(OC)c1OC
Reaction #79332
Tert-butyl 5-(3,4,5-trimethoxyphenyl)-1,2,6b,7,8,10,11,11a-octahydro-9H-azepino[4,5-b][1,4]oxazino[2,3,4-hi]indole-9-carboxylate
収率 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cn([C@H]3CC[C@H](N4CCNCC4C)CC3)c3ncnc(Cl)c23)ccc1Oc1ccccc1
Reaction #79850
title compound
収率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cccc(-c3cccc(C(F)(F)F)n3)c2)ccc1OCc1ccccc1
Reaction #90263
2-(4′-(benzyloxy)-3′-methoxybiphenyl-3-yl)-6-(trifluoromethyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(B(O)O)c(I)c(C)c1OC
Reaction #158235
pure product
収率 56.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(I)c(B(O)O)cc1OC
Reaction #158236
pure product
収率 67.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cnc3[nH]ccc3c2N2CCN(C(=O)[C@H](CN(C(=O)OC(C)(C)C)C(C)C)c3ccc(Cl)cc3)CC2)cc1OC
Reaction #166722
(S)-tert-butyl 2-(4-chlorophenyl)-3-(4-(5-(3,4-dimethoxyphenyl)-1H-pyrrolo[2,3-b]pyridin-4-yl)piperazin-1-yl)-3-oxopropyl(isopropyl)carbamate
収率 18.3%DOI: 10.6084/m9.figshare.5104873.v1
c1cc2c(cc1-c1cncc(N3CC4CC5CC3CN(C5)C4)c1)OCCO2
Reaction #167603
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cncc(N3CC4CC5CC3CN(C5)C4)c2)cc(OC)c1OC
Reaction #167605
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cncc(N3CC4CC5CC3CN(C5)C4)c2)cc1OC
Reaction #167618
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.c1cc2c(cc1-c1ccc(N3CCN(C4CC4)CC3)nn1)OCCO2
Reaction #168106
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cnc3[nH]cc(-c4ccc5[nH]ccc5c4)c3c2)cc(OC)c1OC
Reaction #172196
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncc(-c2cnc3[nH]cc(-c4cnc(N)nc4)c3c2)cn1
Reaction #172197
Compound W
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ccc(-c2cnc3[nH]cc(-c4ccc(N(C)C)nc4)c3c2)cn1
Reaction #172198
Compound X
DOI: 10.6084/m9.figshare.5104873.v1
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