子结构搜索

436682

CC(C)(C)OC(=O)N1CCC(C#N)(CCOS(C)(=O)=O)CC1
Reaction #67983
tert-butyl 4-cyano-4-(2-((methylsulfonyl)oxy)ethyl)piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(C)cc(=O)n(CCC3(C#N)CCN(C(=O)OC(C)(C)C)CC3)c2c1
Reaction #67984
tert-butyl 4-cyano-4-(2-(7-methoxy-4-methyl-2-oxo-1,2-dihydroquinolin-1-yl)ethyl)piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Cl.N#CC1(CO)CCNCC1
Reaction #157964
4-(hydroxymethyl)piperidine-4-carbonitrile hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC2(CC1)CN(C(=O)OCc1ccccc1)C2
Reaction #157973
2-benzyl 7-tert-butyl 2,7-diazaspiro[3.5]nonane-2,7-dicarboxylate
收率 85.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(C#N)CC1C(=O)OCC(=O)c1ccc2cc(Br)ccc2c1
Reaction #159106
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(C#N)CC1c1ncc(-c2ccc(Br)cc2)[nH]1
Reaction #159111
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(C#N)CC1c1ncc(-c2ccc(Br)cc2)[nH]1
Reaction #159115
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CC2(CC2)CC1c1ncc(-c2ccc(-c3ccc4cc(-c5cnc(C6CC(C#N)CN6C(=O)OC(C)(C)C)[nH]5)ccc4c3)cc2)[nH]1)C(C)C
Reaction #159155
title compound
收率 51.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CC2(CC2)CC1c1ncc(-c2ccc(-c3ccc4cc(-c5cnc(C6CC(C#N)CN6)[nH]5)ccc4c3)cc2)[nH]1)C(C)C.Cl.Cl.Cl
Reaction #159156
title compound
收率 92.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CC2(CC2)CC1c1ncc(-c2ccc3cc(-c4ccc(-c5cnc(C6CC(C#N)CN6C(=O)OC(C)(C)C)[nH]5)cc4)ccc3c2)[nH]1)C(C)C
Reaction #159160
title compound
收率 68.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CC2(CC2)CC1c1ncc(-c2ccc3cc(-c4ccc(-c5cnc(C6CC(C#N)CN6)[nH]5)cc4)ccc3c2)[nH]1)C(C)C.Cl.Cl.Cl
Reaction #159161
title compound
收率 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(C#N)CC1C(=O)NCC(=O)c1ccc(Br)cc1
Reaction #159232
2-[2-(4-Bromo-phenyl)-2-oxo-ethylcarbamoyl]-4-cyano-pyrrolidine-1-carboxylic acid tert-butyl ester
收率 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(C#N)CC1c1ncc(-c2ccc(Br)cc2)[nH]1
Reaction #159233
2-[5-(4-Bromo-phenyl)-1H-imidazol-2-yl]-4-cyano-pyrrolidine-1-carboxylic acid tert-butyl ester
收率 35.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC1c1ncc(-c2ccc3cc(-c4ccc(-c5cnc(C6CC(C#N)CN6C(=O)OC(C)(C)C)[nH]5)cc4)ccc3c2)[nH]1
Reaction #159234
2-[5-(4-{6-[2-(1-tert-Butoxycarbonyl-pyrrolidin-2-yl)-3H-imidazol-4-yl]-naphthalen-2-yl}-phenyl)-1H-imidazol-2-yl]-4-cyano-pyrrolidine-1-carboxylic acid tert-butyl ester
收率 33.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](CCC#N)c1ccccc1
Reaction #159522
product
收率 107.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(C#N)CC1C(=O)OCC(=O)c1ccc2cc(Br)ccc2c1
Reaction #167054
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(C#N)CC1c1ncc(-c2ccc(Br)cc2)[nH]1
Reaction #167059
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(C#N)CC1c1ncc(-c2ccc(Br)cc2)[nH]1
Reaction #167063
Title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CC2(CC2)CC1c1ncc(-c2ccc(-c3ccc4cc(-c5cnc(C6CC(C#N)CN6C(=O)OC(C)(C)C)[nH]5)ccc4c3)cc2)[nH]1)C(C)C
Reaction #167100
title compound
收率 51.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC(C(=O)N1CC2(CC2)CC1c1ncc(-c2ccc(-c3ccc4cc(-c5cnc(C6CC(C#N)CN6)[nH]5)ccc4c3)cc2)[nH]1)C(C)C.Cl.Cl.Cl
Reaction #167101
title compound
收率 92.0%DOI: 10.6084/m9.figshare.5104873.v1
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