Recherche de Sous-structure

418863

CCC1(C(=O)O)CN(C(=O)OC(C)(C)C)C1
Reaction #58632
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC1(C(=O)O)CCN1C(=O)OC(C)(C)C
Reaction #58633
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(C(=O)O[C@H]2CC[C@@]3(C)C(C2)C(=O)C[C@@H]2[C@@H]3CC[C@]3(C)C(=O)CC[C@@H]23)C1
Reaction #70406
3β-(N-(tert-Butoxycarbonyl)azetidin-3-ylcarbonyloxy)androstane-6,17-dione
Rendement 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(C(=O)Nc2cnn3ccc(N4CCC[C@@H]4c4cc(F)ccc4Cl)nc23)C1
Reaction #92291
final product
Rendement 61.5%DOI: 10.6084/m9.figshare.5104873.v1
CON(C)C(=O)C1CN(C(=O)OC(C)(C)C)C1
Reaction #92567
crude product
Rendement 127.9%DOI: 10.6084/m9.figshare.5104873.v1
CSc1nn(-c2ccccc2)c2cc(NC(=O)C3CN(C(=O)OC(C)(C)C)C3)ccc12
Reaction #155860
tert-butyl 3-((3-(methylthio)-1-phenyl-1H-indazol-6-yl)carbamoyl)azetidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(c2ccc(Cl)cn2)CN(C(=O)OC(C)(C)C)C1
Reaction #156709
3-(5-Chloro-pyridin-2-yl)-azetidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CON(C)C(=O)C1CN(C(=O)OC(C)(C)C)C1
Reaction #159585
title compound ( D26 )
Rendement 879.8%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #170233
solid
Rendement 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC1(C(=O)O)CCN1C(=O)OC(C)(C)C
Reaction #180862
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CC(C(=O)N2CCC2)C1
Reaction #205302
DOI: 10.1039/C8SC04228D
CCC(=O)CCCCCC(NC(=O)C1CN(C(=O)OC(C)(C)C)C1)c1nc(Br)cn1COCC[Si](C)(C)C
Reaction #228084
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CC(CO)C1
Reaction #269397
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CC(C(=O)NC(Cc2ccc(Cl)c(Cl)c2)C(=O)N2CCN(c3ccccc3NS(C)(=O)=O)CC2)C1
Reaction #275550
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CC(C(=O)OC2CCC3(C)C(C2)C(=O)CC2C4CCC(=O)C4(C)CCC23)C1
Reaction #293455
DOI: 10.1039/C8SC04228D
CON(C)C(=O)C1CN(C(=O)OC(C)(C)C)C1
Reaction #308385
4
Rendement 99.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(C(=O)N[C@H](Cc2ccc(Cl)c(Cl)c2)C(=O)N2CCN(c3ccccc3NS(C)(=O)=O)CC2)C1
Reaction #315268
tert-Butyl 3-{N-[(1R)-1-[(3,4-dichlorophenyl)methyl]-2-(4-{2-[(methylsulfonyl)amino]phenyl}piperazinyl)-2-oxoethyl]carbamoyl}azetidinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(C(=O)N[C@H](Cc2ccc(Cl)cc2)C(=O)N2CCN(c3ccccc3N(CC3CC3)S(C)(=O)=O)CC2)C1
Reaction #315282
tert-Butyl 3-{N-[(1R)-1-[(4-Chlorophenyl)methyl]-2-(4-{2-[(cyclopropylmethyl)(methylsulfonyl)amino]phenyl}-piperazinyl)-2-oxoethyl]carbamoyl}-azetidine-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CON(C)C(=O)C1CN(C(=O)OC(C)(C)C)C1
Reaction #324478
title compound
Rendement 84.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1(CO)CN(C(=O)OC(C)(C)C)C1
Reaction #324674
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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