Busqueda de Subestructura

Cc1ccccc1

CCC(C)(CN=[N+]=[N-])NC(=O)OCc1ccccc1
Reaction #5652
1-Azido-2-(benyloxycarbonylamino)-2-methylbutane
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(-c2ccc(Cl)cc2)cc1C1=C(OC)CCC1=O
Reaction #68746
2-(4′-chloro-4-ethylbiphen-3-yl)-3-methoxycyclopent-2-enone
Rendimiento 75.5%DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(-c2ccc(Cl)cc2)cc1C1C(=O)CCC1=O
Reaction #68747
2-(4′-chloro-4-ethylbiphen-3-yl)-1,3-cyclopentanedione
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C2CC(C(=O)O)Nc3cc(Cl)cc(Cl)c32)cc1
Reaction #75652
Compound 20
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CC(c2cccc(Br)c2)c2c(Cl)cc(Cl)cc2N1
Reaction #75670
Compound 38
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)nc(Oc2ccc3scc(C)c3c2C=O)n1
Reaction #80271
desired compound
Rendimiento 86.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)nc(Oc2ccc3scc(C)c3c2C(=O)O)n1
Reaction #80272
desired compound
Rendimiento 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1C(=O)CC(C)(C)c2ccc(C#C[Si](C)(C)C)cc21
Reaction #80728
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC1(OC)CCC(CN2C(=O)c3ccccc3C2=O)N(C(=O)c2ccccc2-c2ccccc2)C1
Reaction #89090
2-((1-(biphenylcarbonyl)-5,5-dimethoxypiperidin-2-yl)methyl)isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
CN1c2ccccc2C(C(=O)Cl)c2ccccc21
Reaction #155388
10-Methylacridan-9-carboxylic acid chloride
DOI: 10.6084/m9.figshare.5104873.v1
CN1c2ccccc2C(C(=O)Cl)c2ccccc21
Reaction #155390
acid chloride
DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc(-c2ccccc2)c1COc1cc(OCc2ccccc2)ccn1
Reaction #170344
title compound
Rendimiento 28.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc(-c2ccccc2)c1COc1ccc(C(=O)N[C@H](CO)CC(C)C)cn1
Reaction #170511
title compound
Rendimiento 49.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1CCOCC1)c1ccc(OCc2conc2-c2ccc(Cl)cc2)nc1
Reaction #170622
title compound
Rendimiento 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](Nc1nc(Cl)c(C#N)cc1F)C1(NC(=O)OCc2ccccc2)CC1
Reaction #172095
(R)-benzyl 1-(1-(6-chloro-5-cyano-3-fluoropyridin-2-ylamino)propyl)cyclopropylcarbamate
Rendimiento 44.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1)N1CCC(Nc2cc(Cl)cc3cc(-c4ccccc4)[nH]c23)CC1
Reaction #185424
DOI: 10.1039/C8SC04228D
CN1CCC(N(C)C(=O)C2CNc3ccccc32)CC1
Reaction #185613
DOI: 10.1039/C8SC04228D
COC(=O)C1=C(O)CCc2ccc(Br)cc21
Reaction #188088
DOI: 10.1039/C8SC04228D
O=C(C=Cc1ccc(Cl)cc1)C1(Cl)CC1
Reaction #188500
DOI: 10.1039/C8SC04228D
CCCCCCCNC(=O)N(C)c1cccc(-c2ccc(C=C(OCC)C(=O)O)cc2)c1
Reaction #194977
DOI: 10.1039/C8SC04228D
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