2-(3-bromophenyl)-1,3-dioxolane

O=C1C(=O)N(c2cccc(C3OC=CO3)c2)c2ccccc21
Reaction #6699
N-[3-(1,3-dioxolyl)phenyl]isatin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1C(=O)N(c2cccc(C3OC=CO3)c2)c2ccccc21
Reaction #11298
N-[3-(1,3-dioxolyl)phenyl]isatin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[Si](C)(C)C#Cc1cccc(C2OCCO2)c1
Reaction #58827
{[3-(1,3-dioxolan-2-yl)phenyl]ethynyl}-(trimethyl)silane
Yield 74.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
BrCCCCc1cccc(C2OCCO2)c1
Reaction #70666
2-(3-(4-bromobutyl)phenyl)-1,3-dioxolane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1cccc(Nc2cccc(C3OCCO3)c2)c1
Reaction #70671
N-(3-(1,3-dioxolan-2-yl)phenyl)-3-methylaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
c1cc(Nc2cccc3ccccc23)cc(C2OCCO2)c1
Reaction #70673
N-(3-(1,3-dioxolan-2-yl)phenyl)naphthalen-1-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
BrCCCCc1cccc(C2OCCO2)c1
Reaction #70674
2-(3-(4-bromobutyl)phenyl)-1,3-dioxolane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
OC(c1ccccc1)c1cccc(C2OCCO2)c1
Reaction #181952
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1ccc(CN2CCC(Nc3cccc(C4OCCO4)c3)CC2)cc1
Reaction #190903
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1ccc(Nc2cccc(C3OCCO3)c2)nc1
Reaction #194943
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OC(c1cccc(C2OCCO2)c1)c1cccc(C(F)(F)F)c1
Reaction #217530
(3-(1,3-dioxolan-2-yl)phenyl)[3-(trifluoromethyl)phenyl]-methan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
C=C(C)c1cccc(C2OCCO2)c1
Reaction #223053
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(C(O)c2cccc(C3OCCO3)c2)s1
Reaction #272405
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Nc1ccc(Cl)cc1C(=O)c1cccc(C2OCCO2)c1
Reaction #363024
3-(2-amino-5-chlorobenzoyl)phenyl-1,3-dioxolane
Yield 57.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
O=C1C(=O)N(c2cccc(C3OC=CO3)c2)c2ccccc21
Reaction #364526
N-[3-(1,3-dioxolyl)phenyl]isatin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
OC(c1cccc(C2OCCO2)c1)c1cccc(C(F)(F)F)c1
Reaction #370432
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
N#CC(OCCO)c1cccc(Br)c1
Reaction #493541
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
CCCCCCNc1cccc(C2OCCO2)c1
Reaction #499966
title compound
Yield 94.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
C#CCc1cccc(C2OCCO2)c1
Reaction #501311
3(2-propynyl)benzaldehyde ethylene acetal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_12
OCCOCc1cccc(Br)c1
Reaction #746082
2-(3-bromobenzyloxy)ethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
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