子结构搜索

683556

CC1(c2ccccc2)OC(=O)C(Cl)(Cl)C(C(Cl)(Cl)Cl)N1OC(=O)Nc1ccccc1
Reaction #54970
product
收率 39.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(=O)C(Cl)P(=O)(OC(C)C)c1ccccc1
Reaction #56364
1-methylethyl 2-chloro-2[(1-methylethoxy)phenylphosphinyl]acetate
收率 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Oc1ccc(OC)cc1)Oc1ccc(OC)cc1
Reaction #56391
Ethyl 2,2-bis(4-methoxyphenoxy)-acetate
收率 76.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Oc1ccc(C)cc1)Oc1ccc(C)cc1
Reaction #56392
Ethyl 2,2-bis(4-methylphenoxy)acetate
收率 77.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Sc1ccc(C)cc1)Sc1ccc(C)cc1
Reaction #56393
Ethyl 2,2-bis(4-methylthiophenoxy)acetate
收率 68.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cc(Cl)c(Cl)nc1Cl
Reaction #81577
2,3,5,6-tetrachloropyridine
收率 62.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CCCN(Cc2ccc(OC)cc2)C1.Cl
Reaction #94138
methyl N-(p-methoxybenzyl)nipecotate hydrochloride
收率 63.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cl)(Cl)C1OC(=O)C2C1C2(C)C
Reaction #95319
ethyl α,α-dichloro-6,6-dimethyl-4-oxo-3-oxabicyclo[3.1.0]hexane-2-acetate
收率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C12CCC(NCC(=O)N3CC(F)CC3C#N)(CC1)CC2
Reaction #184277
DOI: 10.1039/C8SC04228D
COCCCCCC(=O)c1ccc2c(c1)OCO2
Reaction #184568
DOI: 10.1039/C8SC04228D
CCOC(=O)C1Oc2cc(C)c(S(=O)(=O)c3ccc(C)cc3)cc2O1
Reaction #186983
DOI: 10.1039/C8SC04228D
CCOC(=O)C(Cl)(Cl)CCCCCCCCCCCCSc1ccc(NC(=O)c2ccc(Cl)cc2)cc1
Reaction #187118
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)C1(Cl)OC1(C)C1CCCC1
Reaction #202237
DOI: 10.1039/C8SC04228D
CCOP(=O)(OCC)C(Cl)(Cl)C(=O)OC(C)CC
Reaction #202327
DOI: 10.1039/C8SC04228D
CCOC(=O)C(Cl)(Cl)CCCCCCCCCCS(=O)c1ccc(Cl)cc1
Reaction #205197
DOI: 10.1039/C8SC04228D
CC(C)(CCl)C(OC(=O)C(Cl)Cl)C(Oc1ccc(Cl)cc1)n1ccnc1
Reaction #214063
1-(4-chlorophenoxy)-1-(imidazol-1-yl)-2-dichloroacetoxy-3,3-dimethyl-4-chloro-butane
收率 29.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCC#CCCC(=O)c1ccco1
Reaction #228280
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)Cc1cc(N)ccc1S(=O)(=O)Nc1ccc2c(c1)B(O)OC2
Reaction #255216
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(SCCCCCCCCCCCCC(Cl)(Cl)C(=O)O)cc1)c1ccc(Cl)cc1
Reaction #261666
DOI: 10.1039/C8SC04228D
Cc1cc(C)c(C(=O)CCCc2cccs2)o1
Reaction #269316
DOI: 10.1039/C8SC04228D
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