Busqueda de Subestructura

6229

O=C(OCc1ccccc1)N1CCC(=CCc2ccc(F)cc2)CC1
Reaction #40648
title compound
Rendimiento 17.2%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1cccc2[nH]c(C3(N)CCN(C(=O)OCc4ccccc4)CC3)nc12
Reaction #40913
desired product
Rendimiento 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CN(C(=O)OCc2ccccc2)CC[C@@H]1NC(=O)OC(C)(C)C
Reaction #43641
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(=O)n(C)c(C3CCCN(C(=O)OCc4ccccc4)C3)c(-c3ccccc3)c2c1
Reaction #46144
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(=O)n(C)c(C3CCCNC3)c(-c3ccccc3)c2c1
Reaction #46145
titled product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(=O)n(C)c(C3CCN(C(=O)OCc4ccccc4)CC3)c(-c3ccccc3)c2c1
Reaction #46150
benzyl-4-(6-methoxy-2-methyl-1-oxo-4-phenyl-1,2-dihydroisoquinolin-3-yl)piperidine-1-carboxylate
Rendimiento 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C2CCN(C(=O)OCc3ccccc3)CC2)C(=O)C1
Reaction #48502
title compound
Rendimiento 117.8%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1ccc2[nH]nc(-c3ccccc3)c2c1)C1CCNCC1
Reaction #53741
N-(3-phenyl-1H-indazol-5-yl)piperidine-4-sulfonamide
Rendimiento 11.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=CC2(CC1)CCN(C(=O)OCc1ccccc1)CC2
Reaction #90495
title compound
Rendimiento 57.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CN(C(=O)OCc2ccccc2)CCC1O
Reaction #157073
(+/−)-benzyl 3-(tert-butoxycarbonylamino)-4-hydroxypiperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H]1CCN(C(=O)OCc2ccccc2)C[C@H]1O
Reaction #157074
trans (+/−)-Benzyl 4-(tert-butoxycarbonylamino)-3-hydroxypiperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CN(C(=O)OCc2ccccc2)CCC1F
Reaction #157075
(+/−)-benzyl 3-(tert-butoxycarbonylamino)-4-fluoropiperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CN(C(=O)OCc2ccccc2)CCC1=O
Reaction #157077
(+/−)-Benzyl 3-(tert-butoxycarbonylamino)-4-oxopiperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CN(C(=O)OCc2ccccc2)CC[C@@H]1OS(C)(=O)=O
Reaction #157179
crude product
Rendimiento 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CN(C(=O)OCc2ccccc2)CCC1O
Reaction #160692
(+/−)-benzyl 3-(tert-butoxycarbonylamino)-4-hydroxypiperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H]1CCN(C(=O)OCc2ccccc2)C[C@H]1O
Reaction #160693
trans(+/−)-Benzyl 4-(tert-butoxycarbonylamino)-3-hydroxypiperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CN(C(=O)OCc2ccccc2)CCC1F
Reaction #160695
(+/−)-benzyl 3-(tert-butoxycarbonylamino)-4-fluoropiperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(C(=O)OC(C)(C)C)[C@@H]1CN(C(=O)OCc2ccccc2)CC[C@H]1O
Reaction #160704
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
Reaction #161672
benzyl 4-(2-oxo-2,3-dihydro-imidazo[4,5-b]pyridin-1-yl)-piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CN(C(=O)OCc2ccccc2)CC[C@H]1NC(=O)OC(C)(C)C
Reaction #168531
benzyl (3R,4R)-4-tert-butoxycarbonylamino-3-methoxy-piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Página 1Siguiente