部分構造検索

BrCc1cccc2ccccc12

CCCCC1N=C(I)C(C=O)(Cc2ccc(C(=O)OC)c3ccccc23)N1

収率 85.0%DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)c1ccc(CBr)c2ccccc12

Reaction #11954

収率 96.6%DOI: 10.6084/m9.figshare.5104873.v1

O=C(O)c1ccc(CNc2ccccn2)c2ccccc12

Reaction #11970

収率 9.5%DOI: 10.6084/m9.figshare.5104873.v1

CC(C)(C)OC(=O)N1C[C@H](OCc2cccc3ccccc23)C[C@H]1C(=O)O

Reaction #61358

収率 56.2%DOI: 10.6084/m9.figshare.5104873.v1

CCCCc1nc(I)c(C=O)n1Cc1ccc(C(=O)OC)c2ccccc12

Reaction #65283

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

BrC(c1ccccc1)c1cccc2ccccc12

Reaction #69602

収率 138.5%DOI: 10.6084/m9.figshare.5104873.v1

Cc1ccc2cccc(NC(c3ccccc3)c3cccc4ccccc34)c2n1

Reaction #69603

title compound A5

収率 12.0%DOI: 10.6084/m9.figshare.5104873.v1

Cc1nc2c([N+](=O)[O-])cc(Br)cc2n1Cc1cccc2ccccc12

Reaction #72743

desired product

収率 100.0%DOI: 10.6084/m9.figshare.5104873.v1

CC(C)c1nc2c([N+](=O)[O-])cc(Br)cc2n1Cc1cccc2ccccc12

Reaction #72760

収率 102.6%DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)c1cc(N2CCOCC2)cc2c1nc(C)n2Cc1cccc2ccccc12

Reaction #72782

desired product

収率 74.0%DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)c1cc(N2CCOCC2)cc2c1nc(C(F)(F)F)n2Cc1cccc2ccccc12

Reaction #72803

methyl 6-(4-morpholinyl)-1-(1-naphthalenylmethyl)-2-(trifluoromethyl)-1H-benzimidazole-4-carboxylate

収率 69.2%DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)c1cc(N2CCOCC2)cc2c1nc(C(F)F)n2Cc1cccc2ccccc12

Reaction #72827

desired product

収率 98.0%DOI: 10.6084/m9.figshare.5104873.v1

COc1cccc2ccccc12

Reaction #184157

DOI: 10.1039/C8SC04228D

Clc1ccc2nccc(CBr)c2c1

Reaction #187123

DOI: 10.1039/C8SC04228D

BrCc1cc2c3ccccc3ccc2c2ccccc12

Reaction #191027

DOI: 10.1039/C8SC04228D

COC(=O)c1cc2sccc2n1Cc1cccc2ccccc12

Reaction #197645

DOI: 10.1039/C8SC04228D

BrCc1ccc2sc3ccc4ccccc4c3c2c1

Reaction #208800

DOI: 10.1039/C8SC04228D

BrCc1c2ccccc2cc2ccccc12

Reaction #222036

DOI: 10.1039/C8SC04228D

O=C(O)c1ccc(CO)c2ccccc12

Reaction #250169

DOI: 10.1039/C8SC04228D

BrCc1cccc2ccccc12

Reaction #251388

DOI: 10.1039/C8SC04228D

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