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728991

O=S(=O)(c1ccccc1)N1C=C2C=COC=C3C2=C(C1)CC31OCCO1
Reaction #53612
titled compound ( 34 )
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC2=C3C(=CN(S(=O)(=O)c4ccccc4)C2)C=COC=C13
Reaction #53613
titled compound ( 35 )
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(OCC)c1cc(C(CC#N)n2cc(-c3ncnc4c3ccn4COCC[Si](C)(C)C)cn2)cs1
Reaction #69229
3-[5-(diethoxymethyl)-3-thienyl]-3-[4-(7-[2-(trimethylsilyl)ethoxy]methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]propanenitrile
Ausbeute 43.2%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #69230
residue
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(OCC)c1cc(C(CC#N)n2cc(-c3ncnc4c3ccn4COCC[Si](C)(C)C)cn2)cs1
Reaction #73259
3-[5-(diethoxymethyl)-3-thienyl]-3-[4-(7-[2-(trimethylsilyl)ethoxy]methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]propanenitrile
Ausbeute 43.2%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #73260
residue
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(C2(CCCN3CCc4c(c5c(C(F)(F)F)ccc6c5n4CCS6)C3)OCCO2)cc1
Reaction #79260
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cn(C3CCC(=O)CC3)c3ncnc(N)c23)ccc1N
Reaction #79845
4-[4-amino-5-(4-amino-3-methoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]-1-cyclohexanone
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
O[C@H](CCl)Cc1cc2c(c(-c3ccccc3)c1-c1ccccc1)OCO2
Reaction #82434
title compound
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CCC4CC(OCC(=O)NO[C@@H]5O[C@H](CO)[C@@H](O[C@H]6O[C@H](CO)[C@@H](O[C@H]7O[C@H](CO)[C@@H](O)[C@H](O)[C@H]7O)[C@H](O)[C@H]6O)[C@H](O)[C@H]5O)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #162041
white solid
Ausbeute 74.7%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(SCc2ccccc2)cc1
Reaction #165415
title compound
Ausbeute 94.6%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)[C@@H]1CC[C@]2(NCCN3CCS(=O)(=O)CC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(c6ccc(C(=O)O[C@H]7O[C@H](C(=O)O)[C@@H](O)[C@H](O)[C@H]7O)cc6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
Reaction #172893
desired product
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(C(CC2CCC(=O)C2)c2cc3cccnc3[nH]2)cc1
Reaction #176397
DOI: 10.1039/C8SC04228D
COc1ccc2c(C(=O)c3ccc(OCCN4CCCCC4)cc3)c(-c3ccccc3C=O)sc2c1
Reaction #182601
DOI: 10.1039/C8SC04228D
CC(C)CC(C(=O)O)C(C)NOC1CCCCO1
Reaction #194164
DOI: 10.1039/C8SC04228D
CCCC12COC(C3CCC(C=C(Br)Br)CC3)(OC1)OC2
Reaction #197103
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)c1nc(N2CCc3cccc(C(=O)Nc4nc5ccccc5s4)c3C2)ccc1CCC=O
Reaction #199974
DOI: 10.1039/C8SC04228D
Cn1ccc2cc(-c3ccc(S(=O)(=O)n4ccc(C=CC(=O)NO)c4)cc3)ccc21
Reaction #201698
DOI: 10.1039/C8SC04228D
COC1(OCCc2nc(C(C)C)c(Sc3cc(Cl)cc(Cl)c3)n2C)c2ccccc2-c2ccccc21
Reaction #208133
DOI: 10.1039/C8SC04228D
CC(C)Nn1c(CCCCN2CCN(c3ccc4ccccc4n3)CC2)nc2c(c1=O)CC1(CC2)OCCO1
Reaction #209423
DOI: 10.1039/C8SC04228D
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