sodium ethoxide

COc1ccc(/C=C\c2ccncc2)cc1OC1CCCC1
Reaction #1018
compound
المردود 11.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)C1C2CCCCC2CCN1C(=O)OC
Reaction #1690
title compound
المردود 95.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1nc(O)cc(O)n1
Reaction #3142
4,6-dihydroxy-2-methylpyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)OC(=O)OCC
Reaction #5845
diethyl pyrocarbonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOC(=O)C(Cc1cccc(OC)c1OCc1ccccc1)(NC(C)=O)C(=O)OCC
Reaction #5998
pure crystalline product
المردود 66.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOP(=O)(COCCO)OCC
Reaction #6338
title compound
المردود 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(Nc1ccc([N+](=O)[O-])cc1)c1ccc(O)cc1
Reaction #6509
4-Hydroxy-4'-nitrobenzanilide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(Nc1ccc([N+](=O)[O-])cc1)c1ccc(O)cc1
Reaction #6514
4-Hydroxy-4'-nitrobenzanilide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOC(=O)c1ccc(NC(N)=S)nc1
Reaction #6977
6-thioureido-nicotinic acid ethyl ester
المردود 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Fc1cc(F)c2[nH]ccc2c1
Reaction #8209
5,7-difluoro-indole
المردود 78.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)c1oc2nc(-c3ccc(Cl)cc3Cl)c(-c3ccc(Cl)cc3)cc2c1N
Reaction #8879
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)COc1ccc(O)cc1C
Reaction #9721
solution
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)C(C)(C)Oc1ccc(O)cc1C
Reaction #9724
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1nc(NCC(c2ccccc2)c2ccccc2)c2ncn([C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)c2n1
Reaction #10564
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1C(=O)CC#N
Reaction #11822
title compound
المردود 74.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOc1c(Cl)cc2c([nH]c3cnccc32)c1[N+](=O)[O-]
Reaction #40460
desired product
المردود 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCNc1nccc(C(C)=O)n1
Reaction #40545
1-(2-Ethylaminopyrimidin-4-yl)ethanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(OC)c(-n2nnc(C(=O)O)c2-c2ccc(F)cc2)cc1Cl
Reaction #40717
1-(5-Chloro-2,4-dimethoxy-phenyl)-5-(4-fluoro-phenyl)-1H-[1,2,3]triazole-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)/C(=C/C=C/c1ccc(C)cc1)N=[N+]=[N-]
Reaction #40813
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C/C(=C(\O)c1ccccc1)c1ccccc1
Reaction #40847
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
الصفحة 1التالي