An 88 Reaktionen beteiligt

834203

O=C(OCc1ccccc1)c1ccc(OCc2ccccc2)cc1
Reaction #81358
phenylmethyl 4-(phenylmethoxy)benzoate
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
C(=Cc1ccccc1)c1ccccc1
Reaction #202685
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(C=Cc1ccccc1)Nc1ccc(S(=O)(=O)O)cc1
Reaction #238834
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(OCc1ccccc1)c1ccc(OCc2ccccc2)cc1
Reaction #246879
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
N#CC(=O)c1ccccc1
Reaction #254145
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CN(C)Cc1ccccc1
Reaction #269304
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
[Br-]
Reaction #295638
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCO[Si](OCC)(OCC)C(C)[N+](C)(C)Cc1ccccc1.[Br-]
Reaction #346137
alpha-(benzyldimethylammonio)ethyltriethoxysilane bromide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_07
N#CC=Cc1ccc(Br)cc1
Reaction #392104
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCOCC(O)COc1ccc(-c2nc(-c3ccc(C)cc3C)nc(-c3ccc(C)cc3C)n2)c(O)c1
Reaction #394461
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CN(C)Cc1ccccc1
Reaction #400987
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cn1nnnc1SCC1=C(C(=O)O)N2C(=O)C(NC(=O)C(OC3CCCCO3)c3csc(NS(C)(=O)=O)n3)[C@H]2SC1
Reaction #412577
3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-7-[2-(2-tetrahydropyranyl)oxy-2-(2-mesylamino-1,3-thiazol-4-yl)acetamido]-3-cephem-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_04
CCCCC(CC)COCC1CNC(=O)O1
Reaction #413586
5-(2-ethylhexyl) oxymethyl-2-oxazolidinone
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
CCCCCCCCCCCCCCCCCCOCC1CNC(=O)O1
Reaction #413587
5-stearyloxymethyl-2- oxazolidinone
Ausbeute 290.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
—
Reaction #416836
15.9
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1990_01
CC(C)C(=O)O.CCOc1cc(C=O)ccc1O
Reaction #450469
ethylvanillin isobutyrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_02
O=C1OC2(CCN(C(=O)Nc3cnc(-c4ccccc4)cn3)CC2)c2ccccc21
Reaction #479973
compound
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_10
CCCCOCC(O)COc1ccc(-c2nc(-c3ccc(C)cc3C)nc(-c3ccc(C)cc3C)n2)c(O)c1
Reaction #483914
2-[2-hydroxy-4(3-butoxy-2-hydroxypropyloxy)-phenyl]-4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
CN(C)Cc1ccc(S(=O)(=O)Cl)cc1
Reaction #498789
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
C=CC[N+](C)(C)Cc1ccccc1.[Cl-]
Reaction #524215
Allyl benzyl dimethylammonium chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_06
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