部分構造検索

CCCC=O

Nc1ncnc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O

DOI: 10.6084/m9.figshare.5104873.v1

CCNC(=O)C1OC(n2cnc3c(N)nc(C#CC4(O)CCCCC4C)nc32)C(O)C1O

Reaction #44344

5-[6-Amino-2-(1-hydroxy-2-methyl-cyclohexylethynyl)-purin-9-yl]-3,4-dihydroxytetrahydrofuran-2-carboxylic acid ethylamide

収率 65.0%DOI: 10.6084/m9.figshare.5104873.v1

CCNC(=O)C1OC(n2cnc3c(N)nc(C#CC4(O)CCCC(C)C4)nc32)C(O)C1O

Reaction #44345

5-[6-Amino-2-(1-hydroxy-3-methyl-cyclohexylethynyl)-purin-9-yl]-3,4-dihydroxytetrahydrofuran-2-carboxylic acid ethylamide

DOI: 10.6084/m9.figshare.5104873.v1

CC(C)(C)OC(=O)N1CCCC(N)CC1

Reaction #44480

DOI: 10.6084/m9.figshare.5104873.v1

Nc1ncnc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O

Reaction #50344

DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)C(O)[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@H](O)[C@@H]1O

Reaction #56253

adenosine-5'-carboxylic acid ethyl ester

収率 78.0%DOI: 10.6084/m9.figshare.5104873.v1

COc1cc2nc(N3CCN(C(=O)C4CCCO4)CC3)nc(N)c2cc1OC.C[O-].Cl

Reaction #64276

1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-4-(tetrahydro-2-furoyl)piperazine monohydrochloride methanolate

収率 77.8%DOI: 10.6084/m9.figshare.5104873.v1

COc1cc2nc(N3CCN(C(=O)C4CCCO4)CC3)nc(N)c2cc1OC.C[O-].Cl

Reaction #64277

1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-4-(tetrahydro-2-furoyl)piperazine monohydrochloride methanolate

収率 87.0%DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)C1=C(OS(=O)(=O)c2ccc([N+](=O)[O-])cc2)C(=O)O[C@@H]1C

Reaction #83733

(R)-2-(4-nitrobenzenesulphonyloxy)-3-methoxycarbonyl -2penten-4-olide

DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)C1=C(NCc2ccccc2)C(=O)O[C@@H]1C

Reaction #83734

(R)-2-benzylamino-3-methoxycarbonyl-2-penten-4-olide

DOI: 10.6084/m9.figshare.5104873.v1

CC1(C)C[C@@H](O)[C@H](NC(=O)OCC[Si](C)(C)C)CO1

Reaction #84713

収率 52.0%DOI: 10.6084/m9.figshare.5104873.v1

CC1(C)C[C@H](O)[C@@H](NC(=O)OCC[Si](C)(C)C)CO1

Reaction #84718

収率 86.4%DOI: 10.6084/m9.figshare.5104873.v1

CC(C)(C)OC(=O)N1CCCC(O)(c2cccc(Br)n2)CC1

Reaction #86227

tert-butyl 4-(6-bromopyridin-2-yl)-4-hydroxyazepane-1-carboxylate

収率 64.1%DOI: 10.6084/m9.figshare.5104873.v1

N[C@@]1(C(=O)O)CN(CC2CCCN2)C[C@@H]1CCCB(O)O

Reaction #89660

(3R,4S)-3-amino-4-(3-boronopropyl)-1-(pyrrolidin-2-ylmethyl)pyrrolidine-3-carboxylic acid

収率 96.3%DOI: 10.6084/m9.figshare.5104873.v1

$COc1cc2c(cc1N1CCOCC1)C/C(=C\c1ccc(SC(F)(F)F)cc1)C2=O$

Reaction #90526

crude compound 73

DOI: 10.6084/m9.figshare.5104873.v1

COc1cc2c(cc1N1CCOCC1)CC(Cc1ccc(SC(F)(F)F)cc1)C2=O

Reaction #90527

crude compound 74

DOI: 10.6084/m9.figshare.5104873.v1

O=C1c2cc(S(=O)(=O)NCc3ccccc3)c(Cl)cc2CC1Br

Reaction #94215

6-Benzylsulfamoyl-2-bromo-5-chloro-1-indanone

DOI: 10.6084/m9.figshare.5104873.v1

CC(C)[C@@H](Nc1nc(N2CCN(c3ccc(Cl)cc3)CC2)nc2c1SCC2)C(N)=O

Reaction #157269

収率 88.2%DOI: 10.6084/m9.figshare.5104873.v1

$COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(C(C)(C)C)cc2)c2ccc(C(C)OC(=S)SC)c(OC)n2)c(OC)c1$

Reaction #157836

O-[1-(6-{(E)-1-(4-tert-butylphenyl)-2-[(2R)-1-(2,4-dimethoxybenzyl)-5-oxopyrrolidin-2-yl]ethenyl}-2-methoxypyridin-3-yl)ethyl] S-methyl carbonodithioate

DOI: 10.6084/m9.figshare.5104873.v1

CCc1ccc(/C(=C/[C@H]2CCC(=O)N2Cc2ccc(OC)cc2OC)c2ccc(C(C)(C)C)cc2)nc1OC

Reaction #157837

(5R)-5-[(E)-2-(4-tert-butylphenyl)-2-(5-ethyl-6-methoxypyridin-2-yl)ethenyl]-1-(2,4-dimethoxybenzyl)pyrrolidin-2-one

収率 71.6%DOI: 10.6084/m9.figshare.5104873.v1

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