部分構造検索

11737

Fc1cc(-c2ccsc2)cc(F)c1F
Reaction #3169
3(3,4,5-trifluorophenyl)thiophene
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2nc3cc(C#N)ccc3o2)ccc1-c1ccccn1
Reaction #7867
5-cyano-2-(3-methoxy-4-pyridin-2-ylphenyl)-1,3-benzoxazole
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2nccc(-c3c(-c4ccccn4)nn4c3CCC4)c2c1
Reaction #8342
4-(2-Pyridin-2-yl-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl)-quinoline-6-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccc2c(c1)nc(N)c1nc(CCC)n(CC(C)C)c12
Reaction #9563
1-(2-methylpropyl)-2-propyl-7-vinyl-1H-imidazo[4,5-c]quinolin-4-amine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(CC(=O)c2ccc(-c3ccc([N+](=O)[O-])cc3)cc2)CCOCC1
Reaction #9632
methyl 4-[2-(4′-nitro-1,1′-biphenyl-4-yl)-2-oxoethyl]tetrahydro-2H-pyran-4-carboxylate
収率 79.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1CCCC[C@@H]1C(=O)c1ccc(-c2ccc(N)cc2)cc1
Reaction #9635
methyl cis-2-[(4′-amino-1,1′-biphenyl-4-yl)carbonyl]cyclohexanecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H]1C(=O)c1ccc(-c2ccc(N)cc2)cc1
Reaction #9641
methyl trans-2-[(4′-amino-1,1′-biphenyl-4-yl)carbonyl]-cyclopropanecarboxylate
収率 66.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1CCC[C@H]1C(=O)c1ccc(-c2ccc(N)cc2)cc1
Reaction #9644
methyl trans-2-[(4′-amino-1,1′-biphenyl-4-yl)carbonyl]-cyclopentanecarboxylate
収率 67.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H]1CCC[C@H]1C(=O)c1ccc(-c2ccc(Nc3nc4ccc(Cl)cc4s3)c(F)c2)cc1
Reaction #9706
desired product
収率 60.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2oc(Nc3ccc(-c4ccc(C(=O)[C@@H]5CCCC[C@H]5C(=O)OCC[Si](C)(C)C)cc4)cc3)nc2c1
Reaction #9715
trans-2-(trimethylsilyl)ethyl-2-({4′-[(5-methyl-1,3-benzoxazol-2-yl)amino]biphenyl-4-yl}carbonyl)cyclohexanecarboxylate
収率 50.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C(CCC(N)=O)N1Cc2c(C#N)cccc2C1=O
Reaction #10157
tert-butyl 2-(4-cyano-1-oxoisoindolin-2-yl)-4-carbamoylbutanoate
収率 74.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CCCN1CCc1nc2cc(-c3ccc(C#N)cc3)ccc2[nH]1
Reaction #10513
title compound
収率 40.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(NCC(c2ccccc2)c2ccccc2)c2ncn(C3CCCCO3)c2n1
Reaction #10561
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CC[C@H](Oc2cccc3cncc(C#N)c23)CC1
Reaction #10662
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(-c2nc(Nc3cc(C)n[nH]3)c3ccccc3n2)c1
Reaction #11921
solid
収率 101.8%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc2c(n1)N1[C@H](C2)CN(C(=O)OC(C)(C)C)C[C@H]1C
Reaction #12012
product
収率 89.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C(=O)OC(C)(C)C)C[C@H]2Cc3ccc(C#N)nc3N21
Reaction #12018
desired compound
収率 98.4%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CCOCn1nc(-c2ccnc(C3CC3)n2)cc(-c2nc3ccccc3n2COCC[Si](C)(C)C)c1=O
Reaction #40574
6-(2-Cyclopropylpyrimidin-4-yl)-2-(2-trimethylsilanylethoxymethyl)-4-[1-(2-trimethylsilanylethoxymethyl)-1H-benzimidazol-2-yl]-2H-pyridazin-3-one
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ncc(-c2ccccc2)c(-c2ccccc2)n1
Reaction #40850
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Clc1nccc(-c2cccnc2)n1
Reaction #41752
2-chloro-4-(3-pyridyl)pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
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