propan-2-one

O=C(Nc1ccc(NC(=S)Nc2ccccc2)cc1)c1ccc(NC(=S)Nc2ccccc2)cc1
Reaction #850
colorless crystal
Выход 72.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(Nc1ccc(NC(=S)NCc2ccccc2)cc1)c1ccc(NC(=S)NCc2ccccc2)cc1
Reaction #851
colorless crystal
Выход 43.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)=O.CO.O=C([O-])CC(O)(CC(=O)[O-])C(=O)[O-]
Reaction #857
Citrate Acetone MeOH
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)=O.CO.O=C([O-])CC(O)(CC(=O)[O-])C(=O)[O-]
Reaction #858
Citrate Acetone MeOH
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1c(N)ccc([N+](=O)[O-])c1C
Reaction #903
Methyl 2-methyl-3-nitro-6-aminobenzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CSC[C@H](Nc1cc(F)ccc1[N+](=O)[O-])C(=O)O
Reaction #972
N-(5-Fluoro-2-nitrophenyl)-S-methyl-L-cysteine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CC(F)=C(F)F
Reaction #1038
3,4,4-trifluoro-3-butenoic
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)CC(F)(Cl)C(F)(F)Br
Reaction #1041
4-bromo-3-chloro-3,4,4-trifluorobutanoic acid
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1c(OC2CCC(=O)CC2)ccnc1C
Reaction #1112
4-(4-Oxocyclohexyloxy)-3-methoxy-2-methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCn1ncc(C(=O)c2ccc3c(c2C)C(=NOC)CCS3(=O)=O)c1OCC(=O)c1ccccc1
Reaction #1163
4-methoxyimino-5-methyl-6-(1-ethyl-5-phenacyloxypyrazol-4-yl)carbonylthiochroman-1,1-dioxide
Выход 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
c1ccc2c(c1)ccn1cccc21
Reaction #1269
pyrrolo[2,1-a]isoquinoline
Выход 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)c1ccc(I)nc1
Reaction #1320
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC1=Cc2c(-c3ccccc3)cccc2C1O
Reaction #1353
desired product
Выход 100.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C=CCn1c(=O)n(C)c(=O)n(-c2cc(N=c3sc(=O)n4n3CCCC4)c(F)cc2Cl)c1=O
Reaction #1585
title product
Выход 73.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Oc1cccc(C[C@H]2CO2)c1OCc1ccccc1
Reaction #1614
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Oc1cccc(OCc2ccccc2)c1C[C@H]1CO1
Reaction #1615
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Oc1ccc(OCc2ccccc2)cc1C[C@H]1CO1
Reaction #1616
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)C1(C(=O)OCC)Oc2ccc(C[C@@H](C)NC(=O)OC(C)(C)C)cc2O1
Reaction #1620
(R)-5-[N-(t-Butyloxycarbonyl)-2-aminopropyl]-1,3-benzodioxole-2,2-dicarboxylic acid, diethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)COc1ccc(C[C@@H](C)NC(=O)OC(C)(C)C)cc1
Reaction #1625
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)c1cn2c3c([nH]c(=O)c2n1)-c1cc(Cl)ccc1C3
Reaction #1701
ethyl 7-chloro-4,5-dihydro-4-oxo-10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-2-carboxylate
Выход 61.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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