子结构搜索

937755

CNC(=O)c1c(Nc2cc(Nc3cn(C)nc3C)ncc2C(F)(F)F)cccc1OC
Reaction #238
收率 75.0%
CNC(=O)c1c(Nc2cc(Nc3cn(C)nc3C)ncc2C(F)(F)F)cccc1OC
Reaction #239
收率 58.5%
CNC(=O)c1c(Nc2cc(Nc3cn(C)nc3C)ncc2C(F)(F)F)cccc1OC
Reaction #240
收率 47.5%
CNC(=O)c1c(Nc2cc(Nc3cn(C)nc3C)ncc2C(F)(F)F)cccc1OC
Reaction #241
收率 52.5%
CNC(=O)c1c(Nc2cc(Cl)ncc2C(F)(F)F)cccc1OC
Reaction #258
收率 63.8%
CNC(=O)c1c(Nc2cc(Cl)ncc2C(F)(F)F)cccc1OC
Reaction #259
收率 66.1%
CNC(=O)c1c(Nc2cc(Cl)ncc2C(F)(F)F)cccc1OC
Reaction #260
收率 85.5%
CNC(=O)c1c(Nc2cc(Nc3cc(C)nn3C)ncc2C(F)(F)F)cccc1OC
Reaction #292
收率 46.0%
CNC(=O)c1c(Nc2cc(Nc3cc(C)nn3C)ncc2C(F)(F)F)cccc1OC
Reaction #293
收率 41.6%
COc1cccc(N)c1C(=O)O
Reaction #3208
benzoic acid
收率 100.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc2[nH]c(=O)oc(=O)c12
Reaction #3209
title compound
收率 283.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cc1c(OC)cccc1[N+](=O)[O-])(NC(C)=O)C(=O)OCC
Reaction #11667
diethyl 2-acetylamino-2-(2-methoxy-6-nitrobenzyl)malonate
收率 80.8%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NCCCC(=O)N1CCc2c(OC(CO)CO)ccc([N+](=O)[O-])c21
Reaction #44852
27
收率 78.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cc1c(OC)cccc1[N+](=O)[O-])(NC(C)=O)C(=O)OCC
Reaction #59392
diethyl 2-acetylamino-2-(2-methoxy-6-nitrobenzyl)malonate
收率 80.8%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(N)cccc1OC(F)F
Reaction #67499
2-amino-6-difluoromethoxy-benzonitrile
收率 121.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(OC(F)F)cccc1S(=O)(=O)Cl
Reaction #67500
2-Cyano-3-difluoromethoxy-benzenesulfonyl chloride
收率 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(NC(=O)NC(=O)c2ccccc2)c1C#N
Reaction #72665
N-(2-cyano-3-methoxyphenylcarbamoyl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2cccnc2c1C(=O)O
Reaction #92484
title compound
收率 20.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(C)=O)c(NC(=O)c2cccc(C(C)C)n2)c1C
Reaction #178217
DOI: 10.1039/C8SC04228D
COc1cccc2c1C(C)C(=O)N2
Reaction #184673
DOI: 10.1039/C8SC04228D
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