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499224

CCOC(=O)C(=CNc1ccc(F)cc1F)C(=O)c1c(F)cc(F)c(F)c1C
Reaction #1385
ethyl 2-(2-methyl-3,4,6-trifluorobenzoyl)-3-(2,4-difluorophenyl)aminoacrylate
Ausbeute 87.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cn(-c2ccc(F)cc2F)c2cc(F)c(F)c(C)c2c1=O
Reaction #1386
ethyl 1-(2,4-difluorophenyl)-5-methyl-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)c2c(c1O)C(=O)C(c1ccccc1)C2
Reaction #5088
2,3-dihydro-4,6-dimethyl-2-phenyl-7-hydroxy-1H-inden-1-one
Ausbeute 70.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)c2c(c1O)C(NCc1ccccc1)=C(c1ccccc1)C2
Reaction #5096
4,6-dimethyl-7-hydroxy-1-benzylamino-2-phenyl-3H-indene
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cncn1C1c2ccccc2C(=O)CC1(C)C
Reaction #5869
1-(2,2-dimethyl-4-oxo-tetralin-1-yl)-5-imidazolecarboxylic acid methyl ester
Ausbeute 28.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCC1CC(=O)c2ccc(OC)cc21
Reaction #7972
5-methoxy-3-propyl-1-indanone
Ausbeute 15.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCC1c2cc(OC)ccc2C(=O)C1CCC1(CC)OCCO1
Reaction #7973
2-[2-(2-ethyl-[1,3]dioxolan-2-yl)-ethyl]-5-methoxy-3-propyl-1-indanone
Ausbeute 29.1%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)CCC1(CCO)Cc2cc(OC)ccc2C1=O
Reaction #7997
2-(2-hydroxyethyl)-5-methoxy-2-(3-oxopentyl)-1-indanone
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)(C)CC(=O)c1ccc(-c2ccc(N)c(OC)c2)cc1
Reaction #9653
methyl 4-(4′-amino-3′-methoxy-1,1′-biphenyl-4-yl)-2,2-dimethyl-4-oxobutanoate
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCN3CCOCC3)cc2C1=O
Reaction #46156
title compound
Ausbeute 128.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2cc(OCCCc3ccccc3)ccc2C(c2ccccc2)C1Br
Reaction #46166
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=O
Reaction #46174
title compound
Ausbeute 75.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=O.[NH-]C1CCCCC1
Reaction #46175
title compound
Ausbeute 59.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCN3CCOCC3)cc2C1=O
Reaction #47809
titled compound
Ausbeute 506.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(c2ccccc2)c2ccc(OCCN3CCOCC3)cc2C1(O)c1ccccc1
Reaction #47810
titled compound
Ausbeute 44.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1=O
Reaction #47817
titled compound
Ausbeute 62.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=C(c2ccccc2)c2ccc(OCCCc3ccccc3)cc2C1(O)c1ccccc1
Reaction #47818
titled compound
Ausbeute 90.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC1(O)CCC(C)(C)c2ccc(N=Nc3ccc(C(=O)OCC)cc3)cc21
Reaction #52857
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(N=Nc2ccc3c(c2)C(O)CCC3(C)C)cc1
Reaction #52858
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)(C)CC(=O)c1ccc(-c2ccc(N)c(OC)c2)cc1
Reaction #59150
methyl 4-(4′-amino-3′-methoxy-1,1′-biphenyl-4-yl)-2,2-dimethyl-4-oxobutanoate
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
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