An 136 Reaktionen beteiligt

1328

CCOP(=O)(CCCn1c(=O)c2c(ncn2CC2CC2)n(C)c1=O)OCC
Reaction #2133
Diethyl [3-(7-cyclopropylmethyl-3-methylxanthin-1-yl)propyl]phosphonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOP(=O)(CCCCCn1c(=O)c2c(ncn2CC2CC2)n(C)c1=O)OCC
Reaction #2135
Diethyl [5-(7-cyclopropylmethyl-3-methylxanthin-1-yl)pentyl]phosphonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CP(C)(=O)Cn1c(=O)c2c(ncn2CC2CC2)n(-c2ccccc2)c1=O
Reaction #2150
[1-(7-Cyclopropylmethyl-3-phenylxanthin-1-yl)methyl]dimethylphosphine Oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Oc1ccc(CCOCC2CC2)cc1
Reaction #3090
4-[(2-Cyclopropylmethoxy)-ethyl]-phenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cc(OCC2CC2)c(C=O)cc1-c1cccs1
Reaction #10735
2-Cyclopropylmethoxy-4-methoxy-5-thiophen-2-yl-benzaldehyde
Ausbeute 18.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Brc1ccc(OCC2CC2)cc1
Reaction #68838
1-Bromo-4-cyclopropylmethoxybenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
NCc1cccc(OCC2CC2)c1
Reaction #69061
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
NCc1ccc(F)c(OCC2CC2)c1
Reaction #69062
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
NC(c1ccccc1)c1cccc(OCC2CC2)c1
Reaction #69063
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(N)c1cccc(OCC2CC2)c1
Reaction #69064
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
NC(c1ccc(F)cc1)c1ccc(F)c(OCC2CC2)c1
Reaction #69066
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(N)c1ccc(F)c(OCC2CC2)c1
Reaction #69067
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CNCCc1cccc(OCC2CC2)c1
Reaction #69071
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=Cc1cccc(OCC2CC2)c1
Reaction #165153
title compound
Ausbeute 99.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)N1CCC(COCC2CC2)C1
Reaction #203712
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)N1c2ccc(OCC3CC3)cc2C(C)(c2ccccc2)CC1(C)C
Reaction #206387
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(C2=CCCN(CC3CC3)C2)c1
Reaction #239065
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)c1c(-c2ccc(OC)cc2)c(-c2ccc(OC)cc2)nn(CC2CC2)c1=O
Reaction #252813
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
c1cc2c(cc1-c1nnc(SCC3CC3)o1)CCO2
Reaction #253628
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(=O)c1cc(-c2ccc(SC)cc2)nn(CC2CC2)c1=O
Reaction #254743
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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