pyridinium

CCCCCCC(C(=O)O)C(O)CC(CCCCC)OCc1ccccc1
Reaction #5723
rac-(2RS,3RS,5SR)-5-benzyloxy-2-hexyl-3-hydroxy-decanoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C1CCC(c2ccc(O)cc2O)CC1
Reaction #51879
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C(NC1CCCCC1)NC1CCCCC1
Reaction #71586
dicyclohexylurea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(NC1CCCCC1)NC1CCCCC1
Reaction #71587
dicyclohexylurea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1cc(Cl)cc(C(C)=O)c1OC
Reaction #173035
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)COc1ccc(CC=O)cc1
Reaction #174587
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN(C)C(=O)CC1(CCCC(=O)O)C=CCCC1
Reaction #175136
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1C(=Cc2ccccc2)SC(=S)N1N=c1sc2ccccc2s1
Reaction #175164
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)CCCCCc1cccc2cncn12
Reaction #175224
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCC(CCc1ccccc1)(CC(=O)C(C(=O)OC)C(CC)c1cccc([N+](=O)[O-])c1)OCOc1ccc(-c2ccccc2)cc1
Reaction #176438
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCNC(=O)c1ccc2cc(C(O)(c3c[nH]cn3)C(C)C)ccc2c1
Reaction #176513
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC=CC1OC(C(=O)OC(C)C)C(C(=O)OC(C)C)O1
Reaction #176661
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(C2(C#Cc3ccccn3)CCC(=O)CC2)cc1OC1CCCC1
Reaction #177310
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCC#CCC#CC=CC=O
Reaction #177891
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCC(=O)c1ccc2cc(OC)ccc2c1
Reaction #178703
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CS(=O)(=O)c1ccc(CC(=O)c2ccc(F)cc2)cc1
Reaction #179062
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)Cc1c([N+](=O)[O-])ccc(O)c1F
Reaction #179265
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=CCNC(=O)OCc1ccccc1
Reaction #179337
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)Oc1ccc(CC(NC(=O)OCc2ccccc2)C2OC(C)(C)OC2C(Cc2ccc(OC(C)(C)C)cc2)NC(=O)OCc2ccccc2)cc1
Reaction #179724
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1(C)COC(c2ccc(C(C)(C)C)cc2C2OCCCO2)=N1
Reaction #180383
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Seite 1Weiter