acetic

O=c1[nH]c(-c2ccccc2)nc(C(F)(F)F)c1Br
Reaction #1542
5-bromo-2-phenyl-6-trifluoromethyl-4(3H)-pyrimidinone
Выход 83.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1cc(-c2ccc(Cl)cc2)c[nH]c1=O
Reaction #1601
3-cyano-5-(4-chlorophenyl)-2-pyridinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1cc(-c2ccc(Cl)cc2)c[nH]c1=O
Reaction #2214
3-cyano-5-(4-chlorophenyl)-2-pyridinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCC(CCC)=C(C#N)C(=O)OCC
Reaction #3764
Ethyl α-cyano-α-(4-heptylidene)acetate
Выход 80000.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(NC(CO)c1ccccc1)c1ccccc1
Reaction #3793
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C/C(O)=C(/C#N)C(=O)c1ccc(F)c(F)c1
Reaction #74839
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
Nc1cc(Cl)nc(N)[n+]1[O-]
Reaction #75108
2,4-diamino-6-chloropyrimidine-3-oxide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
O=C(O)c1ccc2c(c1)COC2=O
Reaction #76811
5-carboxyphthalide
Выход 70.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
N#Cc1ccc2[nH]c3c(c2c1)CC(OC(=O)c1ccccc1)CC3
Reaction #81599
3-benzoyloxy-6-cyano-1,2,3,4-tetrahydrocarbazole
Выход 47.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CC1=C(C)C(=O)C(C)CC1
Reaction #94083
2,3,6-trimethyl-2-cyclohexen-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
N#Cc1nn2c(-c3cccc(C(F)(F)F)c3)ccnc2c1C#N
Reaction #312451
3-Cyano-7-(α,α,α-trifluoro-m-tolyl)pyrazolo-[1,5-a]pyrimidine-2-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_11
O=C(c1ccccc1)c1cnn2c1NCCC2c1ccncc1
Reaction #318695
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_07
Cl.ClCCN(CCCl)Cc1cccs1
Reaction #319054
DCTA
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_07
CC(=O)O[C@H](C)CC[C@@H](C)OC(C)=O
Reaction #323610
(R,R)-2,5-diacetoxyhexane
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
O=C(CCl)Nc1cccc2c(=O)[nH][nH]c(=O)c12
Reaction #328668
2-Chloro-N-(1,4-dioxo-1,2,3,4-tetrahydrophthalazine-5-yl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Cc1nn(-c2ccc(O)cc2F)c(-n2c(C)ccc2C)c1C#N
Reaction #329375
5-(2,5-dimethyl-1H-pyrrol-1-yl)-1-(2-fluoro-4-hydroxyphenyl)-3-methyl-1H-pyrazole-4-carbonitrile
Выход 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
O=CN1CCC(Oc2c(F)c(F)c(F)c(F)c2F)CC1
Reaction #336049
1-formyl-4-(2,3,4,5,6-pentafluorophenoxy)piperidine
Выход 91.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
COc1ccc(CN2C(=O)C(N)C(=O)N(c3ccccc3)c3ccccc32)cc1
Reaction #351211
title compound
Выход 102.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
CCOC(=O)C(C#N)=C(C)c1ccccc1
Reaction #357345
2-Cyano-3-phenyl-but-2-enoic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
CC(C)CN1CCC(CN(C2CN(C(c3ccc(Cl)cc3)c3ccc(Cl)cc3)C2)[SH](=O)=O)CC1
Reaction #364312
N-{1-[bis(4-chloro-phenyl)methyl]azetidin-3-yl}-N-(1-isobutylpiperid-4 -yl)methylsulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
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