HOAc

CCN(CCCOC)C(=N)N
Reaction #859
title compound
Выход 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COCCOCCNC(=N)N
Reaction #860
title compound
Выход 28.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N=C(N)NCCOCCOC(=O)c1ccccc1
Reaction #861
title compound
Выход 62.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC[C@H](NC(=O)[C@H](NC(=O)[C@@H](N)CC(=O)O)[C@H](C)O)c1ccccc1
Reaction #864
α-L-aspartyl-D-threonine (S)-α-ethylbenzylamide
Выход 57.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1c(I)ccc2c1C(=O)NS2(=O)=O
Reaction #906
iodine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CS(=O)(=O)c1nccc(OCC(F)(F)F)n1
Reaction #1013
2-methanesulphonyl-4-(2,2,2-trifluorethoxy)-pyrimidine
Выход 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
c1ccc(Oc2ccc(C3CCNCC3)cc2)cc1
Reaction #1047
compound ( 4 )
Выход 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCc1nccc(N[C@H]2CC[C@@H](c3ccccc3)CC2)c1Br
Reaction #1119
2-Ethyl-3-bromo-4-(cis-4-phenylcyclohexylamino)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)c1ccc(S(C)(=O)=O)cc1
Reaction #1161
4-(methylsulfonyl)acetophenone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1ccc(C(=O)O)cc1NN.Cl
Reaction #1183
3-Hydrazino-4-methylbenzoic acid hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1nc(N)c(N=Nc2ccc(Cl)cc2)c(Cl)n1
Reaction #1262
6-chloro-5-[(4-chlorophenyl)azo]-2,4-pyrimidinediamine
Выход 41.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1nc(N)c(N)c(Cl)n1
Reaction #1263
desired product
Выход 75.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)N[C@@H](COc1ccccc1[N+](=O)[O-])C(=O)O
Reaction #1283
N-[(1,1-Dimethylethoxy)carbonyl]-O-(2-nitrophenyl)-L-serine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)[C@@H](Br)Cc1ccccc1
Reaction #1285
(S)-α-Bromobenzenepropanoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)CCC(=O)c2cc(Br)ccc21
Reaction #1309
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC(CC=Cc1ccccc1Br)(C(=O)O)C(=O)O
Reaction #1357
desired product
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1c(F)c(F)cc2c1c(=O)c(C(=O)O)cn2C1CC1
Reaction #1375
1-cyclopropyl-6,7-difluoro-5-methyl-1,4,-dihydro-4-oxoquinoline-3-carboxylic acid
Выход 92.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1c(F)c(F)cc2c1c(=O)c(C(=O)O)cn2-c1ccc(F)cc1
Reaction #1377
1-(4-fluorophenyl)-5-methyl-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid
Выход 94.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCn1cc(C(=O)O)c(=O)c2c(C)c(F)c(F)cc21
Reaction #1379
1-ethyl-5-methyl-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3- carboxylic acid
Выход 80.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1cccc(N)c1C
Reaction #1381
methyl 2-methyl-3-aminobenzoate
Выход 101.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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