部分構造検索

CCc1cccc(CC)c1

CC(=O)c1cc(Nc2cc(C)[n+](C)c(N)n2)cc(C(C)=O)c1.[I-]

2-amino-4-(3,5-diacetylphenyl)amino-1,6-dimethylpyrimidinium iodide

DOI: 10.6084/m9.figshare.5104873.v1

CC(C)(C)c1cc(SCC(=O)NC2CN3CCC2CC3)cc(C(C)(C)C)c1O.Cl

DOI: 10.6084/m9.figshare.5104873.v1

CC(=O)c1ccc2c(c1)C(C)(C)CCS2

DOI: 10.6084/m9.figshare.5104873.v1

C#Cc1ccc2c(c1)C(C)(C)CCS2

DOI: 10.6084/m9.figshare.5104873.v1

CCc1cccc(C(=O)[C@H](C)NC(=O)OC(C)(C)C)c1

Reaction #41306

subtitle compound

DOI: 10.6084/m9.figshare.5104873.v1

$CCOC(=O)c1ccc(/C=C(\C)c2ccc3c(c2)CCC(C)(C)CS3)cc1$

Reaction #65692

ethyl p-[(E)-2-(2,3,4,5-tetrahydro-3,3-dimethyl-1-benzothiepin-7-yl)propenyl]benzoate

DOI: 10.6084/m9.figshare.5104873.v1

CC=CC(=O)c1ccc2sc3ccc(C(=O)C=CC)cc3c(=O)c2c1

Reaction #66038

2,7-bis-(but-2-enoyl)-thioxanthen-9-one

DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)CCc1cc(CCNS(=O)(=O)c2ccc(Cl)cc2)cc(Cc2ccc(F)cc2)c1

Reaction #81610

収率 73.2%DOI: 10.6084/m9.figshare.5104873.v1

O=C(O)CCc1cc(CCNS(=O)(=O)c2ccc(Cl)cc2)cc(Cc2ccc(F)cc2)c1

Reaction #81611

収率 82.6%DOI: 10.6084/m9.figshare.5104873.v1

CC(=O)c1cc(Nc2cc(C)[n+](C)c(N)n2)cc(C(C)=O)c1.[I-]

Reaction #81889

2-amino-4-(3,5-diacetylphenyl)amino-1,6-dimethylpyrimidinium iodide

DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)[C@@H](Cc1ccc2c(c1)CCN(Cc1ccc(OC)cc1OC)S2(=O)=O)NC(=O)OC(C)(C)C

Reaction #87140

(R)-methyl 2-((tert-butoxycarbonyl)amino)-3-(2-(2,4-dimethoxybenzyl)-1,1-dioxido-3,4-dihydro-2H-benzo[e][1,2]thiazin-6-yl)propanoate

収率 46.0%DOI: 10.6084/m9.figshare.5104873.v1

CC(C)(C)c1cc(SC(Sc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)c2ccccc2)cc(C(C)(C)C)c1O

Reaction #93217

収率 66.3%DOI: 10.6084/m9.figshare.5104873.v1

CC(C)(C)c1cc(SC(Sc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)C2CC=CCC2)cc(C(C)(C)C)c1O

Reaction #93220

収率 113.1%DOI: 10.6084/m9.figshare.5104873.v1

CCc1ccc2c(c1)CCN2S(=O)(=O)c1ccccc1

Reaction #161127

1-benzenesulfonyl-5-ethyl-2,3-dihydro-1H-indole

収率 43.4%DOI: 10.6084/m9.figshare.5104873.v1

CCc1ccc2c(c1)CCN2

Reaction #161128

5-ethyl-2,3-dihydro-1H-indole

収率 34.0%DOI: 10.6084/m9.figshare.5104873.v1

OCc1ccc(-c2ccc(Cc3cc(C4OC(CO)C(O)C(O)C4O)ccc3Cl)s2)cc1

Reaction #182230

DOI: 10.1039/C8SC04228D

COc1c(N(C)C)cc(C(=O)CBr)cc1C(C)(C)C

Reaction #186710

DOI: 10.1039/C8SC04228D

CC(C)(C)c1cc(-n2nc3ccc(S(=O)(=O)c4ccccc4)cc3n2)c(O)c(C(C)(C)C)c1

Reaction #188410

DOI: 10.1039/C8SC04228D

CC(C)(C)c1cc(-n2nc3ccc(S(=O)c4ccccc4)cc3n2)c(O)c(C(C)(C)C)c1

Reaction #188480

DOI: 10.1039/C8SC04228D

CC(=O)c1ccc2c(c1)C(C)(C)CCS2

Reaction #190944

DOI: 10.1039/C8SC04228D

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