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224435

CC1(C)CCC(=O)c2cc(C#Cc3ccc(C(=O)O)cn3)ccc21
Reaction #1330
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C1CCc2cccc(C(=O)C(=CN(C)C)OC)c2C1
Reaction #50425
2-di-n-propylamino-8-(1-oxo-2-methoxy-3-(dimethylamino)-prop-2-enyl)-1,2,3,4-tetrahydronaphthalene
DOI: 10.6084/m9.figshare.5104873.v1
C#Cc1ccc2c(c1)C(C)(C)CCC2N(C)C(C)C
Reaction #52362
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(C#Cc2ccc(CC(=O)OC)cc2)ccc1C1(OCc2ccccc2)CC1
Reaction #52453
title compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(C#Cc2ccc(CC(=O)O)cc2)ccc1C1(OCc2ccccc2)CC1
Reaction #52455
{4-[4-(1-Benzyloxycyclopropyl)-3-ethyl-phenylethynyl]-phenyl}-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(N=Nc2ccc3c(c2)C(OCOC)CCC3(C)C)cc1
Reaction #52859
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(NC(C)C)C(O)c1ccc(OC(=O)C2CCCCC2)c2c1CCC(=O)N2
Reaction #56059
8-cyclohexylcarbonyloxy-5-(1-hydroxy-2-isopropylaminobutyl)-3,4-dihydrocarbostyril
DOI: 10.6084/m9.figshare.5104873.v1
NC1CCCc2cc(OS(=O)(=O)C(F)(F)F)ccc21
Reaction #60383
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC(NS(=O)(=O)c1cccc(C(F)(F)F)c1)c1ccccc1)NC1CCCc2cc(OS(=O)(=O)C(F)(F)F)ccc21
Reaction #60384
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2cc(OC)ccc2c1O
Reaction #63942
final product
Ausbeute 67.0%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
Ausbeute 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
C#Cc1ccc2c(c1)C(C)(C)CCC2N(C)C(C)C
Reaction #79931
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(C#Cc2ccc(CC(=O)OC)cc2)ccc1C1(OCc2ccccc2)CC1
Reaction #80019
title compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(=O)c2cc(C#Cc3ccc(C(=O)O)cn3)ccc21
Reaction #81598
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(=O)c2cc(C#Cc3ccc(C(=O)O)cn3)ccc21
Reaction #81663
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1ccc(C(=O)NC2CCc3c(O)ccc(N4CCN(C)CC4)c3C2)cc1
Reaction #175718
DOI: 10.1039/C8SC04228D
Cc1cc(C(F)(F)F)nn1CC(=O)N1CCN(c2nc(C(=O)N(C)C3CCCc4ccccc43)cs2)CC1
Reaction #194270
DOI: 10.1039/C8SC04228D
CCc1ccc(Cc2cc3c(cc2Cl)C(F)CC32OC(COCc3ccccc3)C(OCc3ccccc3)C(OCc3ccccc3)C2OCc2ccccc2)cc1
Reaction #195291
DOI: 10.1039/C8SC04228D
O=C1CCCN1c1ccc(Oc2ccc3c(c2)CCN(C2CCC2)CC3)nc1
Reaction #203120
DOI: 10.1039/C8SC04228D
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