1-ethylpiperidine

CC(C)(c1ccc(O)cc1)c1ccc(O)cc1.Oc1ccc(Oc2ccc(O)cc2)cc1
Reaction #59223
bisphenol A 4,4′-dihydroxydiphenyl ether
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)(c1ccc(O)cc1)c1ccc(O)cc1.Oc1ccc(Oc2ccc(O)cc2)cc1
Reaction #59224
bisphenol A 4,4′-dihydroxydiphenyl ether
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)(c1ccc(O)cc1)c1ccc(O)cc1.Oc1ccc(Oc2ccc(O)cc2)cc1
Reaction #59225
bisphenol A 4,4′-dihydroxydiphenyl ether
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC1CC(C)(C)CC(c2ccc(O)cc2)(c2ccc(O)cc2)C1.Oc1ccc(Oc2ccc(O)cc2)cc1
Reaction #59226
bisphenol TMC 4,4′-dihydroxydiphenyl ether
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Oc1ccc(-c2ccc(O)cc2)cc1.Oc1ccc(Oc2ccc(O)cc2)cc1
Reaction #59227
4,4′-dihydroxydiphenyl ether 4,4′-dihydroxybiphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Oc1ccc(-c2ccc(O)cc2)cc1.Oc1ccc(Oc2ccc(O)cc2)cc1
Reaction #59228
4,4′-dihydroxydiphenyl ether 4,4′-dihydroxybiphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Oc1ccc(-c2ccc(O)cc2)cc1.Oc1ccc(Oc2ccc(O)cc2)cc1
Reaction #59229
4,4′-dihydroxydiphenyl ether 4,4′-dihydroxybiphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)(c1ccc(O)cc1)c1ccc(O)cc1.Oc1ccc(Oc2ccc(O)cc2)cc1
Reaction #59230
bisphenol A 4,4′-dihydroxydiphenyl ether
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)(c1ccc(O)cc1)c1ccc(O)cc1.Oc1ccc(Oc2ccc(O)cc2)cc1
Reaction #59231
bisphenol A 4,4′-dihydroxydiphenyl ether
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1ccc(CCC(=O)O)cc1OC
Reaction #64702
3-(3,4-dimethoxyphenyl)propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC[C@@H](NC(c1ccccc1)(c1ccccc1)c1ccccc1)C(C)=O
Reaction #168616
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC[C@H](NC(c1ccccc1)(c1ccccc1)c1ccccc1)C(C)=O
Reaction #168617
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COC(=O)C(Cc1ccccc1)NC(=O)C(CC(N)=O)NC(=O)C(CO)NC(=O)OCc1ccccc1
Reaction #195563
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C=CCOC(=O)N1CC(OC(=O)NC)CC1C=C(C)C(=O)CC1NC(=O)C1C(CO[SiH](C)C)C(C)(C)C
Reaction #199172
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCC(NC(c1ccccc1)(c1ccccc1)c1ccccc1)C(C)=O
Reaction #242493
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(O[Si](C)(C)C(C)(C)C)C1C(=O)NC1C(C)C(=O)C(C)(C)O[Si](C)(C)C
Reaction #245007
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(O[Si](C)(C)C(C)(C)C)C1C(=O)NC1C(C)C(=O)N1CCSC1=S
Reaction #246145
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
C=CCOC(=O)N1CC(OC)CC1C=C(C)C(=O)CC1NC(=O)C1C(CO[SiH](C)C)C(C)(C)C
Reaction #280133
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)C(Cc1ccccc1)NC(=O)C(CC(N)=O)NC(=O)OCc1ccccc1
Reaction #282037
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(OC)c1ncn2c(-c3cccnc3)c(C(=O)[C@H](C)[C@H]3NC(=O)[C@@H]3[C@@H](C)O[Si](C)(C)C(C)(C)C)sc12
Reaction #317221
(3S,4R)-3-[(1R)-1-(tert-Butyldimethylsilyloxy)ethyl]-4-[(1R)-1-methyl-2-[7-dimethoxymethyl(pyridin-3-yl)imidazo[5,1-b]thiazol-2-yl]-2-oxoethyl]azetidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
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