methanol

COC(=O)c1cc(Cl)ccc1O
Reaction #856
methyl 5-chlorosalicylate
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
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
Yield 57.5%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)CC)c1ccccc1
Reaction #866
α-L-aspartyl-D-isoleucine (S)-α-ethylbenzylamide
Yield 72.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC[C@H](NC(=O)[C@H](NC(=O)[C@@H](N)CC(=O)O)C(C)C)c1ccccc1
Reaction #870
α-L-aspartyl-D-valine (R)-α-methoxymethylbenzylamide
Yield 70.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC[C@H](NC(=O)[C@H](NC(=O)[C@@H](N)CC(=O)O)C(C)C)c1ccccc1
Reaction #872
α-L-aspartyl-D-valine (R)-α-ethoxymethylbenzylamide
Yield 50.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(CC(=O)c1ccc(Br)cc1)C(=O)c1ccc(Br)cc1
Reaction #889
1,2-Bis(4-bromobenzoyl)-1-methoxyethane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cnn(C)c(=O)c1Br
Reaction #893
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C#CCC1C(=O)N(C)OC1c1ccccc1
Reaction #907
2-methyl-5-phenyl-4-propargylisoxazolin-3-one
Yield 34.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CON=Cc1[nH]ccc1S(=O)(=O)NC(C)(C)C
Reaction #917
title compound
Yield 96.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Fc1cccc(F)c1-c1ccc2cccnc2n1
Reaction #926
desired product
Yield 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
c1cnc2nc(-c3nccs3)ccc2c1
Reaction #927
desired product
Yield 46.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(C)cc(S(=O)c2cccc(F)c2C#N)c1
Reaction #937
2-[(3,5-dimethylphenyl)sulfinyl]-6-fluorobenzonitrile
Yield 47.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(C)cc(S(=O)(=O)c2cccc(F)c2C#N)c1
Reaction #938
2-[(3,5-dimethylphenyl)sulfonyl]-6-fluorobenzonitrile
Yield 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(C)cc(S(=O)c2cccc(N)c2C#N)c1
Reaction #939
2-amino-6-[(3,5-dimethylphenyl)sulfinyl]benzonitrile
Yield 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(C)cc(S(=O)(=O)c2cccc(N)c2C#N)c1
Reaction #940
2-amino-6-[(3,5-dimethylphenyl)sulfonyl]benzonitrile
Yield 57.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)NCC1CNC1
Reaction #966
title compound
Yield 67.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc([N+](=O)[O-])c(N[C@@H](CSC)C(=O)O)c1
Reaction #973
N-(5-Methoxy-2-nitrophenyl)-S-methyl-L-cysteine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)c1coc2c1C(=O)CCC2
Reaction #995
4-oxo-4,5,6,7-tetrahydrobenzofuran-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
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