部分構造検索

Cc1ccc(Br)cn1

Cc1ccc(C2=CCC(C)(C)c3ccc(Br)cc32)cn1
Reaction #2708
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2ccc(C)nc2)c(OC)n1
Reaction #40965
title compound
収率 62.0%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccc(C)nc1
Reaction #66063
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccccc1-c1ccc(Br)cn1
Reaction #70298
5-Bromo-2-(2-fluorophenyl)pyridine
収率 50.0%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc(-c2cnccn2)nc1
Reaction #70301
2-(5-Bromopyridin-2-yl)pyrazine
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
Brc1ccc(-c2cccc(Br)c2)nc1
Reaction #71531
5-bromo-2-(3′-bromophenyl)-pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCC#Cc1ccc(Br)cn1
Reaction #77844
1-2
収率 89.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCC#Cc1ccc(C#CCNC(=O)OCc2ccccc2)cn1
Reaction #77846
6-1
収率 55.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC#Cc1ccc(Br)cn1)OCc1ccccc1
Reaction #77847
7-1
収率 73.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC(=O)c1ncc(Br)cc1Br)c1ccccc1C(F)(F)F
Reaction #84316
desired product
収率 13.7%DOI: 10.6084/m9.figshare.5104873.v1
CCON=C(CNC(=O)c1ccccc1C(F)(F)F)c1ncc(Br)cc1Br
Reaction #84317
desired product
収率 89.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)N2CCN(C)CC2)cc(Br)c(=O)n1C
Reaction #86328
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Oc2cnc3c(c2)c(=O)n(CCCOC2CCCCO2)c(=O)n3C)cn1
Reaction #88712
1-methyl-6-((6-methylpyridin-3-yl)oxy)-3-(3-((tetrahydro-2H-pyran-2-yl)oxy)propyl)pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione
収率 77.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Br)c[n+]1[O-]
Reaction #89279
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Br)c(C#N)n1
Reaction #89280
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(/C(=C/[C@H]2CCC(=O)N2)c2ccc(C(C)(C)C)cc2)ccc1Br
Reaction #157737
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(C(C)(C)C)cc2)c2ccc(/C=C/CCO[Si](C)(C)C(C)(C)C)c(OC)n2)c(OC)c1
Reaction #157843
(5R)-5-[(E)-2-{5-[(1E)-4-{[tert-butyl(dimethyl)silyl]oxy}but-1-en-1-yl]-6-methoxypyridin-2-yl}-2-(4-tert-butylphenyl)ethenyl]-1-(2,4-dimethoxybenzyl)pyrrolidin-2-one
収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(C(C)(C)C)cc2)c2ccc(C#N)c(OC)n2)c(OC)c1
Reaction #157854
6-{(E)-1-(4-tert-butylphenyl)-2-[(2R)-1-(2,4-dimethoxybenzyl)-5-oxopyrrolidin-2-yl]ethenyl}-2-methoxypyridine-3-carbonitrile
収率 40.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CCC2C=C(c2ccc(C(C)(C)C)cc2)c2ccc(C3(O)CCC3)c(OC)n2)c(OC)c1
Reaction #157856
5-{2-(4-tert-butylphenyl)-2-[5-(1-hydroxycyclobutyl)-6-methoxypyridin-2-yl]ethenyl}-1-(2,4-dimethoxybenzyl)pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(C(C)(C)C)cc2)c2ccc(SC)c(OC)n2)c(OC)c1
Reaction #157859
(5R)-5-{(E)-2-(4-tert-butylphenyl)-2-[6-methoxy-5-(methylsulfanyl)pyridin-2-yl]ethenyl}-1-(2,4-dimethoxybenzyl)pyrrolidin-2-one
収率 34.0%DOI: 10.6084/m9.figshare.5104873.v1
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