Recherche de Sous-structure

18499

C=COC1CCC=C1Br

1-bromo-5-vinyloxy-cyclopentene

DOI: 10.6084/m9.figshare.5104873.v1

C=COC1CCC=C1Br

Reaction #57006

1-bromo-5-vinyloxy-cyclopentene

DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)c1ccc(-c2nc([C@@H]3CCCn4c(C5CC5)nnc43)n3ccnc(NCc4ccc(OC)cc4OC)c23)cc1

Reaction #90746

(S)-methyl 4-(3-(3-cyclopropyl-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyridin-8-yl)-8-((2,4-dimethoxybenzyl)amino)imidazo[1,5-a]pyrazin-1-yl)benzoate

Rendement 46.0%DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)C1CCn2c(nnc2C(F)(F)F)C1

Reaction #90752

ethyl 3-(trifluoromethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyridine-7-carboxylate

Rendement 88.9%DOI: 10.6084/m9.figshare.5104873.v1

C=CCCC(OC=C)C(c1ccccc1)c1ccccc1

Reaction #166076

1,1-diphenyl-2-(1-ethenoxy)-hex-5-ene

Rendement 66.0%DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)c1ccc(CN(c2nc3cc(OC)ccc3n2C)C2CCC(C(C)(C)C)CC2)cc1

Reaction #317184

DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)c1ccc(CN(c2nc3cc(OC)ccc3n2C)C2CCC(C(C)(C)C)CC2)c(Br)c1

Reaction #317198

Methyl 3-bromo-4-{[(4-tert-butylcyclohexyl)(5-methoxy-1-methyl-1H-benz-imidazol-2-yl)amino]methyl}benzoate

DOI: 10.6084/m9.figshare.5104873.v1

$COc1ccc(Cl)cc1C(=NC#N)/N=c1\sc(C(C)(C)C)cn1CC1(OC(C)=O)CCCC1$

Reaction #341811

Rendement 75.0%DOI: 10.6084/m9.figshare.5104873.v1

$CCCn1cc(C(C)(C)C)s/c1=N\C(=NC#N)c1cc(C#N)ccc1OC$

Reaction #341812

Rendement 73.8%DOI: 10.6084/m9.figshare.5104873.v1

$COc1ccc(Cl)cc1C(=NC#N)/N=c1\sc(C(C)(C)C)cn1CC1(OC(C)=O)CCC1$

Reaction #341814

Rendement 77.0%DOI: 10.6084/m9.figshare.5104873.v1

$COc1ccc(C(F)(F)F)cc1C(=NC#N)/N=c1\sc(C(C)(C)C)cn1CC1(OC(C)=O)CCC1$

Reaction #341816

Rendement 89.5%DOI: 10.6084/m9.figshare.5104873.v1

$CCOc1ccc(C(F)(F)F)cc1C(=NC#N)/N=c1\sc(C(C)(C)C)cn1C[C@H]1CCCO1$

Reaction #341817

Rendement 309.1%DOI: 10.6084/m9.figshare.5104873.v1

CC1(C)OC(O)C(=O)c2sc(=O)sc21

Reaction #476475

6-hydroxy-4,4-dimethyl-4H-[1,3]dithiolo[4,5-c]pyran-2,7(6H)-dione

DOI: 10.6084/m9.figshare.5104873.v1

CC(C)n1cnc2c(I)c(N)ccc21

Reaction #516740

Rendement 35.0%DOI: 10.6084/m9.figshare.5104873.v1

Brc1cc2nc[nH]c2c(Br)c1NC1=NCCN1

Reaction #516758

desired product

Rendement 86.0%DOI: 10.6084/m9.figshare.5104873.v1

COc1cc(C(=O)N2CCN(C(=O)CCCCC(O)(c3ccc(F)cc3)c3ccc(F)cc3)CC2)cc(OC)c1OC

Reaction #583214

6,6-bis-(4-fluoro-phenyl)-6-hydroxy-1-[4-(3,4,5,-trimethoxy-benzoyl)-piperazin-1-yl]-hexan-1-one

DOI: 10.6084/m9.figshare.5104873.v1

CC(C)(C)OC(=O)N1CCN(c2nnc([C@@H]3CC[C@@H]4CN3C(=O)N4OCc3ccccc3)s2)CC1

Reaction #602813

tert-butyl 4-(5-((2S,5R)-6-(benzyloxy)-7-oxo-1,6-diaza-bicyclo[3.2.1]octan-2-yl)-1,3,4-thiadiazol-2-yl)piperazine-1-carboxylate

Rendement 24.0%DOI: 10.6084/m9.figshare.5104873.v1

[Cl][Hg][CH2][C@H]1O[C@H](COCc2ccccc2)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@@H]1OCc1ccccc1

Reaction #609359

(((2S,3S,4S,5R,6R)-3,4,5-tris(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-yl)methyl)mercury(II) chloride

Rendement 72.0%DOI: 10.6084/m9.figshare.5104873.v1

O[C@@H]1[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@@H](COCc2ccccc2)O[C@@H]1[CH2][Hg][Cl]

Reaction #609363

(((2S,3R,4R,5R,6R)-4,5-bis(benzyloxy)-6-((benzyloxy)methyl)-3-hydroxytetrahydro-2H-pyran-2-yl)methyl)mercury(II) chloride

Rendement 85.2%DOI: 10.6084/m9.figshare.5104873.v1

$COc1ccc(Cl)cc1C(=NC#N)/N=c1\sc(C(C)(C)C)cn1CC1(OC(C)=O)CCCC1$

Reaction #625952

Rendement 75.0%DOI: 10.6084/m9.figshare.5104873.v1