hydroxide

COC(=O)c1cc(N=Nc2ccc(O)c(CC(=O)O)c2)cc(C(=O)OC)c1
Reaction #4515
5-(3,5-bis-(methoxycarbonyl)-phenylazo)-2-hydroxy-phenylacetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CON=C1CC(CO[Si](C)(C)C(C)(C)C)(CO[Si](C)(C)C(C)(C)C)C1
Reaction #6061
title compound
수율 20.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cc1cccc(C(=O)N(NC(=O)C2C=c3ccc4cccc5ccc(c3c54)C2=O)C(C)(C)C)c1
Reaction #49951
N'-t-butyl-N-pyrenonecarbonyl-N'-(3-toluoyl)hydrazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CC[P+](CC)(c1ccccc1)c1ccccc1.[OH-]
Reaction #68704
diphenyldiethylphosphonium hydroxide
수율 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC1=C(C)C(=O)C(C)CC1
Reaction #94087
2,3,6-trimethyl-2-cyclohexen-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
COC(C(=O)NC1CSc2ccccc2N(Cc2ccccc2)C1=O)C(O)C(O)C(O)C=CC(C)(C)C
Reaction #172950
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(CBr)(OC)c1ccc(Cl)cc1Cl
Reaction #172964
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CCc1ccc(NCc2cccc(-c3c(C)cc(OCC4(O)CCS(=O)CC4)cc3C)c2)cc1F
Reaction #172965
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(c1ccc(NC=O)c([N+](=O)[O-])c1)n1ccnc1
Reaction #172970
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C(=O)O)c1ccc2c(c1)Cc1cccnc1O2
Reaction #172975
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(Br)c(C(=O)NC(Cc2ccc(-c3cc(Br)cn(C)c3=O)cc2)C(=O)O)c1
Reaction #172979
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN1CCc2c([nH]c3ccc([N+](=O)[O-])cc23)C1
Reaction #172987
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(COc2nn(Cc3ccccc3)cc2CC(=O)O)ccc1OCc1nc(-c2ccccc2)oc1C
Reaction #172990
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCc1ccc2c(c1)CCC(=O)C2
Reaction #172995
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCP(=O)(O)c1cc(Oc2ncc(Cl)cc2Cl)ccc1[N+](=O)[O-]
Reaction #173002
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1cc2[nH]ccc2c(-c2nc(N3CCOCC3)c3nc(CN4CC(N5CCOCC5)C4)sc3n2)n1
Reaction #173042
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1c(C(=O)NCC(=O)O)nc(Cl)c2ccccc12
Reaction #173044
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(CCCc1ccc(F)cc1)C1CCC(c2ccc3[nH]c(=O)sc3c2)CC1
Reaction #173046
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOCCn1nc(CC)c(N)c1C(N)=O
Reaction #173066
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOCCn1cc(C2CCNCC2)c2ccccc21
Reaction #173075
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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