子结构搜索

1012162

COC1(/C=C/CO)CCOCC1

Reaction #50179

4-methoxy-4-(3-hydroxy -trans-prop-1-enyl)tetrahydropyran

收率 48.0%DOI: 10.6084/m9.figshare.5104873.v1

NCc1cccc(Cc2ccccc2)c1

Reaction #51402

3-(benzyl)benzyl amine

DOI: 10.6084/m9.figshare.5104873.v1

CN(C(=O)OC(C)(C)C)[C@H]1CC[C@H](/C=C/CO)CC1

Reaction #53918

trans-(1E)-[4-(3-Hydroxy-propenyl)-cyclohexyl]-methyl-carbamic acid tert-butyl ester

收率 79.3%DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)c1c(C(C)C)nc(N)c(C=O)c1-c1ccc(F)cc1

Reaction #57366

ethyl 6-amino-4-(4-fluorophenyl)-5-formyl-2-isopropylnicotinate

DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)c1c(C(C)C)nc2c(c1-c1ccc(F)cc1)CCCN2

Reaction #57367

methyl 4-(4-fluorophenyl)-2-isopropyl-5,6,7,8-tetrahydro-[1,8]naphthyridine-3-carboxylate

收率 92.1%DOI: 10.6084/m9.figshare.5104873.v1

Cc1cccc2c1SCCCN2

Reaction #79246

9-methyl-2,3,4,5-tetrahydro-1,5-benzothiazepine

收率 107.3%DOI: 10.6084/m9.figshare.5104873.v1

CC(C)(C)OC(=O)Nc1ccnc(CN2CCOCC2)c1

Reaction #84165

收率 33.0%DOI: 10.6084/m9.figshare.5104873.v1

OCc1ccc2c(c1)OC(F)(F)O2

Reaction #85458

(2,2-difluoro-1,3-benzodioxol-5-yl)-methanol

DOI: 10.6084/m9.figshare.5104873.v1

CC1CCCC2(C)CC(C)(C)OC12

Reaction #89616

2,2,3a,7-tetramethyl-octahydro-benzofuran

收率 62.3%DOI: 10.6084/m9.figshare.5104873.v1

OCc1ccc2c(c1)OC(F)(F)O2

Reaction #169516

(2,2-difluoro-1,3-benzodioxol-5-yl)-methanol

DOI: 10.6084/m9.figshare.5104873.v1

NCc1cccc(Cc2ccccc2)c1

Reaction #220392

3-(benzyl)benzyl amine

DOI: 10.6084/m9.figshare.5104873.v1

CC(C)(C)OC(=O)N1CCC[C@@H]([C@@H](OCCN)c2cccc(Cl)c2)C1

Reaction #305559

(R)-tert-butyl 3-((R)-(2-aminoethoxy)(3-chlorophenyl)methyl)piperidine-1-carboxylate

收率 89.1%DOI: 10.6084/m9.figshare.5104873.v1

CN(CCCc1nc2ccccc2[nH]1)CCC1(O)CC2CCC1C=C2c1cccs1

Reaction #307480

rac-(1R*,2R*,4R*)-2-(2-{[3-(1H-benzoimidazol-2-yl)-propyl]-methyl-amino}-ethyl)-5-thiophen-2-yl-bicyclo[2.2.2]oct-5-en-2-ol

收率 79.7%DOI: 10.6084/m9.figshare.5104873.v1

CN(CCCc1nc(-c2ccccc2)c(-c2ccccc2)n1COCC[Si](C)(C)C)CCC1(O)CC2CCC1C=C2c1ccccc1

Reaction #307496

rac-(1R*,2R*,4R*)-2-[2-({3-[4,5-diphenyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazol-2-yl]-propyl}-methyl-amino)-ethyl]-5-phenyl-bicyclo[2.2.2]oct-5-en-2-ol

收率 97.5%DOI: 10.6084/m9.figshare.5104873.v1

CNCCCN(C)CCC1(O)CC2CCC1C=C2c1ccccc1

Reaction #307499

rac-(1R*,2R*,4R*)-2-{2-[methyl-(3-methylamino-propyl)-amino]-ethyl}-5-phenyl-bicyclo[2.2.2]oct-5-en-2-ol

收率 118.6%DOI: 10.6084/m9.figshare.5104873.v1

CNc1ccc(-c2c(C)sc3ncnc(N)c23)cc1

Reaction #314807

desired product

收率 20.4%DOI: 10.6084/m9.figshare.5104873.v1

CCCCCCCCCCC[C@@H](O)CCO

Reaction #320650

收率 89.0%DOI: 10.6084/m9.figshare.5104873.v1

CCC1OC2(CCN(C)CC2)CC1=O

Reaction #320844

收率 80.3%DOI: 10.6084/m9.figshare.5104873.v1

$CN1CCC2(CC1)CC(N)CO2.O=C(O)/C=C\C(=O)O$

Reaction #320845

DOI: 10.6084/m9.figshare.5104873.v1

CCCCCCCCCCC[C@@H](O)CCO

Reaction #322043

收率 89.0%DOI: 10.6084/m9.figshare.5104873.v1

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