部分構造検索

B(C)(O)O

CCCCc1nc2c(N)nc3cc(/C=C/c4ccccc4)ccc3c2n1CC(C)C
Reaction #9451
2-butyl-1-isobutyl-7-[(E)-2-phenylethenyl]-1H-imidazo[4,5-c]quinolin-4-amine
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
CCCCC(=O)N(Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1)[C@H](C(=O)O)C(C)C
Reaction #40873
Valsartan
収率 55.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(=O)N(Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1)[C@H](C(=O)O)C(C)C
Reaction #40874
Valsartan
収率 85.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(=O)N(Cc1ccc(-c2ccccc2-c2nnn[nH]2)cc1)[C@H](C(=O)O)C(C)C
Reaction #40875
Valsartan
収率 58.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2ccc(-c3ccc(N4CC[C@@H]5CN(C)C[C@@H]54)cc3)cc2)cn1
Reaction #41252
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2ccc(C3CC3)cc2c(N2CCOCC2)c1S(C)(=O)=O
Reaction #41944
white crystals
収率 22.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(Br)c(C=Cc2ccccc2)c(C)c(C#N)c1NC(=O)C(C)(C)C
Reaction #45549
N-(3-Bromo-6-cyano-2-methoxy-5-methyl-4-styrylphenyl)-2,2-dimethylpropionamide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H](CC(C)C)N1CC(Oc2cccc(C3CC3)c2F)=CC1=O
Reaction #47445
(S)-2-[4-(3-cyclopropyl-2-fluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methyl-pentanoic acid ethyl ester
収率 710.3%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(F)c(C2CC2)c1
Reaction #48069
3-cyclopropyl-4-fluorophenylamine
収率 64.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-n2c(C(=O)N3CCC(F)(F)CC3)cc3cc(OC4CCN(C(C)C)CC4)ccc32)cn1
Reaction #48151
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(Oc2cc(O[C@@H](C)CO[Si](C)(C)C(C)(C)C)cc(C(=O)Nc3ccn(C)n3)c2)cc1
Reaction #48846
desired compound
収率 62.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(C3CC3)c3c2C(=O)NC3)cc2cc(CN3CCN(CCO[Si](C)(C)C(C)(C)C)CC3)ccc21
Reaction #49500
4-cyclopropyl-7-{1-(tert-butoxycarbonyl)-5-[4-(2-tert-butyldimethylsilyloxyethyl)pyperazin-1-ylmethyl]indol-2-yl}isoindolinone
収率 68.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)OB(O)c1ccc(CCCCCCCCCCCO)cc1
Reaction #53274
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(B(O)O)cc1)N1CCN(S(=O)(=O)c2cc3cc(Cl)ccc3[nH]2)CC1
Reaction #56675
4-({4-[(5-chloro-1H-indol-2-yl)sulphonyl]piperazin-1-yl}carbonyl)phenyl boronic acid
収率 56.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2ccc(C(=O)O)cc2)cc(C)c1OCCO
Reaction #59033
title compound
収率 38.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(-c2[nH]c3cccc4c3c2CCNC4=O)cc1
Reaction #61608
4-(6-oxo-3,4,5,6-tetrahydro-1H-azepino[5,4,3-cd]indol-2-yl)-benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCCc2c(-c3ccc[nH]3)[nH]c3cccc1c23
Reaction #61618
2-(1H-pyrrol-2-yl)-1,3,4,5-tetrahydro-azepino[5,4,3-cd]indol-6-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1ccc2c(c1)Sc1cccc(-c3cc(=O)cc(N4CCOCC4)o3)c1S2
Reaction #62070
title compound
収率 127.4%DOI: 10.6084/m9.figshare.5104873.v1
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Reaction #62150
succinate salt
DOI: 10.6084/m9.figshare.5104873.v1
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