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Cc1ccccc1P(c1ccccc1C)c1ccccc1C

Cc1ncc(-c2nc(Nc3ccc(CN4CCOCC4)cc3F)ncc2F)n1C1CCOCC1
Reaction #112
Ausbeute 88.0%
CCOC(=O)c1ccc(/C=C/c2cccc3c2C(Sc2ccccc2)=CCC3(C)C)cc1
Reaction #1466
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(/C=C/c2ccc3c(c2)C(SCC)=CCC3(C)C)cc1
Reaction #1467
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C1CCc2cc(/C=C/C(=O)OC)ccc2C1
Reaction #1765
expected product
Ausbeute 28.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC[C@H](NC(=O)c1ccc(C(=Cn2cnc3nc(NC(=O)C(C)(C)C)cc-3c2O)COC2CCCCO2)cc1)C(=O)OCC
Reaction #6625
diethyl N-[4-{1-(tetrahydropyr-2-yloxy)-3-(4-hydroxy-6-pivaloylaminopyrrolo[2,3-d]pyrimidin-3-yl)prop-2-en-2yl}benzoyl]glutamate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CC(=O)Nc2cccc(/C=C/c3cccc(C)c3)c2)ccc1OCCNC(=O)OC(C)(C)C
Reaction #7178
4-[2-(tert-butoxycarbonylamino)-ethoxy]-3-methoxy-N-[3-[(E)-2-(3-methylphenyl)vinyl]phenyl]phenylacetamide
Ausbeute 152.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C=Cc1ccc2c(-c3c(-c4cccc(C)n4)nn4c3CCC4)ccnc2c1
Reaction #8348
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc2c(N)nc3cc(/C=C/c4ccccn4)ccc3c2n1CCCOC
Reaction #9599
(E)-2-ethoxymethyl-1-(3-methoxypropyl)-7-(2-pyridin-2-ylvinyl)-1H-imidazo[4,5-c]quinolin-4-amine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(F)cccc1-c1ccc([C@@H](C)NC(=O)OC(C)(C)C)cc1
Reaction #10163
methyl 4′-{(1R)-1-[(tert-butoxycarbonyl)amino]ethyl}-3-fluoro-1,1′-biphenyl-2-carboxylate
Ausbeute 18.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccccc1-c1ccc(C#N)cc1
Reaction #10166
methyl 4′-cyano-1,1′-biphenyl-2-carboxylate
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=Cc1ccc2c(n1)N1[C@H](C2)CN(C(=O)OC(C)(C)C)C[C@H]1C
Reaction #12015
desired compound
Ausbeute 91.2%DOI: 10.6084/m9.figshare.5104873.v1
C(=C\c1cccc2sccc12)/c1ccccc1
Reaction #43682
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(/C=C/C(=O)OCc2ccccc2)cn1
Reaction #46486
title compound
Ausbeute 39.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCOc2cc(/C=C/C(=O)O)cnc21
Reaction #46497
title compound
Ausbeute 94.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)/C=C/c1ccc2c(c1)CC(=O)N2
Reaction #46519
title compound
Ausbeute 162.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CNc1ccc(/C=C/C(=O)OC(C)(C)C)cn1
Reaction #46533
title compound
Ausbeute 93.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)/C=C/c1cnc2c(c1)CCC(=O)N2
Reaction #46535
title compound
Ausbeute 45.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)/C=C/c1cnc2c(c1)CCCC(=O)N2
Reaction #46572
title compound
Ausbeute 58.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1[nH]c2ccccc2c1CN(C)C(=O)/C=C/c1cnc(N)nc1
Reaction #46588
title compound
Ausbeute 128.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C=C/c1cnc2c(c1)CCC(=O)N2
Reaction #46592
title compound
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1
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