部分構造検索

705447

CC(C)(C)OC(=O)N1CCC(CN)CC1
Reaction #10622
title compound
収率 93.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Nc2cccc3cncc(Cl)c23)CC1
Reaction #10647
title compound
収率 21.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCc2nc(NC(=N)N)sc2C1
Reaction #40338
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(=O)C(Br)C1
Reaction #40339
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(=O)C(C)(C)C1
Reaction #40527
3,3-dimethyl-4-oxo-piperidine-1-carboxylic acid tert-butyl ester
収率 32.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CNCCC1=O
Reaction #40528
3,3-Dimethyl-piperidin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(C2CCNCC2)cn1
Reaction #40580
title compound
収率 52.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(O)(C(Cc2ccc(F)cc2)C(=O)O)CC1
Reaction #40645
69NLS56
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)N1CCC(=CCc2ccc(F)cc2)CC1
Reaction #40648
title compound
収率 17.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Nc2cccnc2N)CC1
Reaction #42657
title compound
収率 33.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(=O)C(C)(C)C1
Reaction #42974
3,3-dimethyl-4-oxo-piperidine-1-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(O)(c2cc(F)ccc2S)CC1
Reaction #43503
crude product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(F)c1C1(O)CCN(C(=O)OC(C)(C)C)CC1
Reaction #43504
4-(2-fluoro-6-methoxy-phenyl)-4-hydroxy-piperidine-1-carboxylic acid tert-butyl ester
収率 31.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCC(O)(c2cc(F)ccc2OC)CC1
Reaction #43505
4-(5-fluoro-2-methoxy-phenyl)-4-hydroxy-piperidine-1-carboxylic acid ethyl ester
収率 99.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(O)(c2ccccc2S)CC1
Reaction #43506
4-Hydroxy-4-(2-mercapto-phenyl)-piperidine-1-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(O)(c2cc(C(F)(F)F)ccc2Sc2ccc(Cl)cc2)CC1
Reaction #43507
compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(=C(Br)C#N)CC1
Reaction #43780
title compound
収率 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1Cc2cn[nH]c2CC1c1ccccc1
Reaction #44001
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCN(C(=O)OCc2ccccc2)C(c2ccc(Cl)cc2)C1
Reaction #44007
product 67
DOI: 10.6084/m9.figshare.5104873.v1
CCC1CC(=O)CC(c2ccc(Cl)cc2)N1C(=O)OCc1ccccc1
Reaction #44013
83
収率 33.3%DOI: 10.6084/m9.figshare.5104873.v1
1 ページ次のページ