部分構造検索

762831

O=C1c2ccccc2C(=O)N1c1ncnc2c1ncn2OCc1ccccc1
Reaction #6347
title compound
収率 49.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1Cc1ccccc1CCl
Reaction #64860
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc(N2C(=O)c3ccccc3C2=O)cc1
Reaction #66415
titled compound
収率 90.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1cnc(N2C(=O)c3ccccc3C2=O)nc1
Reaction #66423
(tert-butoxy)-N-[2-(1,3-dioxobenzo[c]azolidin-2-yl)pyrimidin-5-yl]carboxamide
収率 91.1%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccccc1)c1cc(O)c2c(c1O)C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74964
1,2,3,4,9,9-hexachloro-1,4-dihydro-6-(phenylsulfonyl)-1,4-methanonaphthalene-5,8-diol
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc(O)c2c(c1O)C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74965
1,2,3,4,9,9-hexachloro-1,4-dihydro-5,8-dihydroxy-1,4-methanonaphth-6-yl methyl ketone
DOI: 10.6084/m9.figshare.5104873.v1
Oc1cc(Cl)c(O)c2c1C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74966
1,2,3,4,6,9,9-heptachloro-1,4-dihydro-1,4-methanonaphthalene-5,8-diol
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(O)c2c(c1O)C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
Reaction #74968
crystals
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cn2cc(Oc3cccc(N4Cc5ccccc5C4)c3)ccc2n1)C1CC1
Reaction #191229
DOI: 10.1039/C8SC04228D
COC(=O)C1(C(=O)OC)Cc2cc(OC)c(OC)cc2C1
Reaction #203249
DOI: 10.1039/C8SC04228D
COc1cc2c(cc1OC)CN(CCc1ccc(N)cc1)C2
Reaction #213085
DOI: 10.1039/C8SC04228D
O=C(Oc1ccc(Br)c(Br)c1Br)c1ccccc1CCl
Reaction #235511
DOI: 10.1039/C8SC04228D
O=C1OC(=O)c2cc(Cl)ccc21
Reaction #246949
DOI: 10.1039/C8SC04228D
Cc1c(Br)cccc1N1Cc2ccccc2C1
Reaction #263017
DOI: 10.1039/C8SC04228D
CON=C(Cl)c1ccccc1COc1cccc(Cl)c1
Reaction #282951
DOI: 10.1039/C8SC04228D
O=C1c2ccccc2C(=O)N1c1nc2ccccc2[nH]1
Reaction #290448
DOI: 10.1039/C8SC04228D
CC[P+](CC)(CC)Cc1ccccc1CCl.[Cl-]
Reaction #353180
2-(Chloromethyl)benzyltriethylphosphonium chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCC[P+](CCCC)(CCCC)Cc1ccccc1CCl.[Cl-]
Reaction #353181
2-(Chloromethyl)benzyltri-n-butylphosphonium chloride
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1OC)CN(c1c(C)c(C)c3c(c1C)C(c1ccccc1)C(C)(C)O3)C2
Reaction #359508
title compound
収率 26.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1OC)CN(c1c(C)c(C)c3c(c1C)C(c1ccc(C)cc1)C(C)(C)O3)C2
Reaction #359510
title compound
収率 16.0%DOI: 10.6084/m9.figshare.5104873.v1
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