piperonal

CCOc1ccc2c(c1)c(-c1ccc3c(c1)OCO3)c(C(=O)OC)c(=O)n2Cc1ccccc1OC
Reaction #3003
methyl 4-(1,3-benzodioxol-5-yl)-1,2-dihydro-6-ethoxy-1-(2-methoxybenzyl)-2-oxoquinoline-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=[N+]([O-])/C=C/c1ccc2c(c1)OCO2
Reaction #3096
E-2-(3,4-methylenedioxy)-nitrostyrene
수율 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=[N+]([O-])C=Cc1ccc2c(c1)OCO2
Reaction #3102
3,4-Methylenedioxy-1-(2-nitroethenyl)-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cn1c(-c2ccc3c(c2)OCO3)cc2onc(-c3ccccc3Cl)c2c1=O
Reaction #8408
6-Benzo[1,3]dioxol-5-yl-3-(2-chloro-phenyl)-5-methyl-5H-isoxazolo[4,5-c]pyridin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
c1cnc2c(c1)CCCC2N(Cc1ccc2c(c1)OCO2)Cc1nc2ccccc2[nH]1
Reaction #9058
titled compound
수율 33.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
BrC(Br)=Cc1ccc2c(c1)OCO2
Reaction #52302
title compound
수율 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(C)/N=C1\S/C(=C\c2ccc3c(c2)OCO3)C(=O)N1c1ccccc1
Reaction #66987
5-benzo[1,3]dioxol-5-ylmeth-(Z)-ylidene-2-[(Z)-isopropylimino]-3-phenyl-thiazolidin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(Nc1ccccc1)N1CCN(Cc2ccc3c(c2)OCO3)CC1
Reaction #68891
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(Nc1ccc(F)cc1)N1CCN(Cc2ccc3c(c2)OCO3)CC1
Reaction #68896
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CN(C)CCCN=Cc1ccc2c(c1)OCO2
Reaction #74873
product
수율 75.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
O=[N+]([O-])/C=C/c1ccc2c(c1)OCO2
Reaction #82849
E-2-(3,4-methylenedioxy)-nitrostyrene
수율 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=[N+]([O-])C=Cc1ccc2c(c1)OCO2
Reaction #82855
3,4-Methylenedioxy-1-(2-nitroethenyl)-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cc1cc(OCc2ccccc2)cc2[nH]c(C(=O)O)cc12
Reaction #90932
6-(Benzyloxy)-4-methyl-1H-indole-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cl.OC1(c2ccc3c(c2)OCO3)C(c2ccc(F)cc2)SC2=NCCCCN21
Reaction #95517
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
N#CC(N)c1ccc2c(c1)OCO2
Reaction #175789
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOc1cc(C(O)c2ccc3c(c2)OCO3)ccc1OC
Reaction #189795
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1NC(=S)SC1=Cc1ccc2c(c1)OCO2
Reaction #202654
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cccc(C(O)c2ccc3c(c2)OCO3)c1
Reaction #203185
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C1Cc2c([nH]c3ccccc23)C(c2ccc3c(c2)OCO3)N1
Reaction #203200
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1c(NCc2ccc3c(c2)OCO3)cccc1[N+](=O)[O-]
Reaction #211569
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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