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CC(=O)[O-].[K+]

CC1(C)S[C@@H]2[C@H](NC(=O)CCC[C@H](N)C(=O)O)C(=O)N2[C@H]1C(=O)O
Reaction #1525
isopenicillin N
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)S[C@@H]2[C@H](NC(=O)CCC[C@H](N)C(=O)O)C(=O)N2[C@H]1C(=O)O
Reaction #2780
isopenicillin N
DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])[C@H]1/C(=C/CO)O[C@@H]2CC(=O)N21.[K+]
Reaction #3722
potassium clavulanate
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])c1ccccc1.[K+]
Reaction #4034
Potassium benzoate
Ausbeute 73.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])c1ccccc1.[K+]
Reaction #4039
Potassium benzoate
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1cccnc1C=O
Reaction #7241
3-n-propoxypyridine-2-carboxaldehyde
Ausbeute 113.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(-c2nn3c(c2-c2ccnc4cc(CCC(=O)N(C)C)ccc24)CCC3)n1
Reaction #8366
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(COc2ccc3c(-c4c(-c5ccccn5)nn5c4CCC5)ccnc3c2)C1
Reaction #8372
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])C1OC1C(=O)[O-].[K+].[K+]
Reaction #8648
potassium epoxysuccinate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCc1nc(CO)co1
Reaction #9002
(4-hydroxymethyl-oxazol-2-ylmethyl)-carbamic acid tert-butyl ester
Ausbeute 28.4%DOI: 10.6084/m9.figshare.5104873.v1
OCc1ccc(-c2nc3ccccc3s2)cc1
Reaction #9069
title compound
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #9075
alcohol
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C(=O)OC(C)(C)C)C[C@H]2Cc3ccc(CCCO)nc3N21
Reaction #12016
compound
Ausbeute 50.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](C#N)CC(=O)[O-].[K+]
Reaction #40272
potassium (S)-3-cyano-5-methylhexanoate
Ausbeute 31.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](CN)CC(=O)O
Reaction #40273
(S)-3-aminomethyl-5-methylhexanoic acid
Ausbeute 26.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nnc(C(=O)N[C@@H](C)[C@H](Oc2ccc3c(cnn3-c3ccc(F)cc3)c2)c2ccccc2)o1
Reaction #41420
N-{(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-phenylpropan-2-yl}-5-methyl-[1,3,4]oxadiazol-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc([C@@H](Oc2ccc3c(cnn3-c3ccc(F)cc3)c2)[C@H](C)NC(=O)c2nnc(C)o2)c1
Reaction #41472
N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-(3-methoxyphenyl)propan-2yl]-5-methyl-1,3,4-oxadiazole-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
COC(COC(=O)c1ccccc1)OC
Reaction #41954
compound
Ausbeute 72.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(COC(=O)c1ccccc1)OCC
Reaction #41955
compound
Ausbeute 84.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(COC(=O)c1ccccc1)OCC
Reaction #41956
compound
Ausbeute 34.1%DOI: 10.6084/m9.figshare.5104873.v1
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