類似構造検索

3

Cc1ncc(-c2nc(Nc3ccc(CN4CCOCC4)cc3F)ncc2F)n1C1CCOCC1
Reaction #113
収率 73.0%
CC(C)(C)OC(=O)N1CCN(c2cccs2)CC1
Reaction #398
収率 0.0%
CC(C)(C)OC(=O)N[C@@H]1CCC[C@H](C(=O)Nc2cc(-c3cnn4c3CCCCC4)c(F)cn2)C1
Reaction #613
収率 72.4%
CC1(C)Cc2ncc(-c3cc(NC(=O)[C@H]4CCC[C@@H](NC(=O)OC(C)(C)C)C4)ncc3F)n2C1
Reaction #622
収率 80.0%
CC1(C)CCn2ncc(-c3cc(NC(=O)[C@H]4CCC[C@@H](NC(=O)OC(C)(C)C)C4)ncc3F)c2C1
Reaction #661
収率 52.8%
CC1(C)Cc2c(-c3cc(NC(=O)[C@H]4CCC[C@@H](NC(=O)OC(C)(C)C)C4)ncc3F)cnn2C1
Reaction #663
収率 35.1%
CC1(C)Cc2c(-c3cc(NC(=O)[C@H]4CCC[C@@H](NC(=O)OC(C)(C)C)C4)ncc3F)cnn2C1
Reaction #664
収率 53.6%
CC(C)(C)OC(=O)N[C@@H]1CCC[C@H](C(=O)Nc2cc(-c3cnn4c3CCCC4)c(F)cn2)C1
Reaction #694
収率 37.4%
CC1(C)Cc2c(-c3cc(NC(=O)[C@@H]4CCC[C@@H](NC(=O)OC(C)(C)C)C4)ncc3F)cnn2C1
Reaction #743
収率 84.4%
FC(F)(F)CC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[I-]
Reaction #950
solid
収率 76.5%DOI: 10.6084/m9.figshare.5104873.v1
N=C(NC(=O)OCc1ccccc1)c1ccc(CN)cc1
Reaction #953
4-aminomethyl-1-(N-benzyloxycarbonylamidino)benzene
DOI: 10.6084/m9.figshare.5104873.v1
CC#Cc1cncc(C2CCCN2C)c1
Reaction #1137
5-propynyl-3-(1-methyl-2-pyrrolidinyl)pyridine
収率 312.1%DOI: 10.6084/m9.figshare.5104873.v1
C#CC(C)(O)Cc1cncc(C2CCCN2C(=O)OC(C)(C)C)c1
Reaction #1138
5-(2-hydroxy-2-methyl-3-butynyl)-3-(1-tert-butyloxycarbonyl-2-pyrrolidinyl)pyridine
収率 76.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)N1CCC(N2C(=O)c3ccccc3C2=O)CC1
Reaction #1173
1-benzyloxycarbonyl-4-phthalimidylpiperidine
収率 50.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC#CCn1c(-c2ccccc2)nc(C(F)(F)F)c(CC)c1=O
Reaction #1552
5-ethyl-3-(pent-2-yn-4-en-1-yl)-2-phenyl-6-trifluoromethyl-4(3H)-pyrimidinone
収率 28.4%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(CBr)s1
Reaction #1693
2-cyano-5-(bromomethyl)thiophene
収率 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1ccc(C(=O)Oc2ccc(C(=O)O)cn2)cc1C12CC3CC(CC(C3)C1)C2
Reaction #1739
6-[3-adamantan-1-yl-4-(tert-butyl-dimethyl-silanyloxy)-benzoyloxy]-nicotinic acid
収率 22.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OC(=O)C2CCOCC2)cc1OC
Reaction #1770
methyl 4-(4-tetra-hydropyranoyloxy)-2-methoxy-benzoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OC(=O)[C@@H]2CCCC[C@@H]2c2ccccc2)cc1OC
Reaction #1773
methyl 4-(cis-2-phenyl-1-cyclohexanoyloxy)-2-methoxybenzoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OC(=O)C2CCOc3ccccc32)cc1OC
Reaction #1778
methyl 4-(4-chromanoyloxy)-2-methoxybenzoate
DOI: 10.6084/m9.figshare.5104873.v1
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