Recherche de Sous-structure

NCCCCCO

COC(=O)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
Reaction #1294
title product
Rendement 196.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
Reaction #1430
title product
Rendement 196.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(OCCCCCN2CCCCC2)cc(-c2ccc(F)cc2)n1
Reaction #8796
4-(4-fluorophenyl)-2-methyl-6-(5-piperidinopentyloxy)pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@H]1C(OC(C)=O)O[C@H](COC(C)=O)[C@@H](F)[C@@H]1OC(C)=O
Reaction #11385
2-acetamido-1,3,6-tri-O-acetyl-2,4-dideoxy-4-fluoro-D-glucopyranose
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(OC(c2ccccc2)C2CC(O)CN2C(=O)CCCCCN)c2ccc(OC)cc2)cc1
Reaction #49172
compound 5
Rendement 91.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCC1(C)CCc2c(C)c(OCCOC(=O)NCCCCCC(=O)N3CC(O)CC3C(OC(c3ccc(OC)cc3)c3ccc(OC)cc3)c3ccccc3)c(C)c(C)c2O1
Reaction #49176
Compound 19
Rendement 88.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(OC(c2ccccc2)C2CC(O)CN2CCCCCCN)c2ccc(OC)cc2)cc1
Reaction #49181
compound 31
Rendement 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCNC(=O)CCC(C)C1CCC2C3CCC4CC(OC(=O)NCCCCCC(=O)N5CC(O)CC5C(OC(c5ccc(OC)cc5)c5ccc(OC)cc5)c5ccccc5)CCC4(C)C3CCC12C
Reaction #49209
Compound 90
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2CCC(OC(C)=O)CC2NC(=O)c2ccc(OCC3CC3)c(OCC3CC3)c2)cc1OC
Reaction #58345
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2CCC(OC(C)=O)CC2NC(=O)c2ccc(OCC3CC3)c(OCC3CC3)c2)cc1OC
Reaction #58346
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2CCC(O)CC2NC(=O)c2ccc(OCC3CC3)c(OCC3CC3)c2)cc1OC
Reaction #58347
title compound
Rendement 87.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2CCC(=O)CC2NC(=O)c2ccc(OCC3CC3)c(OCC3CC3)c2)cc1OC
Reaction #58348
title compound
Rendement 91.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2CCC(O)CC2NC(=O)c2ccc(OCC3CC3)c(OCC3CC3)c2)cc1OC
Reaction #58349
title compound
Rendement 68.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CN1CCOCC1)NNC(=O)c1cc(Br)cc2c1cnn2C1CCCCO1
Reaction #67100
title compound
Rendement 70.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@H]1O[C@H](OC(C)=O)[C@H](N)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #77726
amine
Rendement 101.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1N1CCN(CC2CCCN(CC3(c4ccc(Cl)cc4)CC3)C2)CC1
Reaction #78937
desired compound
Rendement 54.8%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)[C@H]1CC[C@@H](OS(C)(=O)=O)[C@H](NS(=O)(=O)NC(=O)OCc2ccccc2)C1
Reaction #92323
title compound
Rendement 72.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cn([C@H]2C[C@H](O)[C@@H](CNC(=O)N(C)N=O)O2)c(=O)[nH]c1=O
Reaction #93937
white fine needles
Rendement 70.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(=S)N[C@@]1(c2cc(Br)ccc2F)CO[C@@H](COCc2ccccc2)C[C@H]1CO)c1ccccc1
Reaction #155595
product
Rendement 63.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H]1CN([C@@H](C)c2ccccc2)CCC1=O
Reaction #167981
(5)-ethyl 4-oxo-1-((S)-1-phenylethyl)piperidine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
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