heptane

CC(C)(C)[Si](C)(C)O[C@H]1C=C[C@@H](O)C1
Reaction #2635
title compound
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)C1C(C)=CC(=O)CC1(C)C
Reaction #4075
ester
Ausbeute 27.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)C(=O)C(=Cc1ccccc1)C(=O)Nc1ccccc1
Reaction #5780
4-methyl-3-oxo-N-phenyl-2-(phenylmethylene)pentanamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=P([O-])([O-])[O-].[Al+3].[Mg+2]
Reaction #5859
aluminum-magnesium phosphate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
[Li][c]1cccc2c1ccc1ccccc12
Reaction #8609
1-lithiophenanthrene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
[Li][c]1cccc2c1ccc1ccccc12
Reaction #8610
1-lithiophenanthrene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(=O)NC[C@H]1CN(c2cccc(F)c2)C(=O)O1
Reaction #8619
title compound
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C#Cc1cccc2nc(NC(=O)NCC)sc12
Reaction #9217
desired compound
Ausbeute 15.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(OC)c(-c2cc3ccccc3s2)cc1/C=C/C(=O)c1ccc(C(=O)O)cc1
Reaction #10717
4-[3-(5-benzo[b]thiophen-2-yl-2,4-dimethoxy-phenyl)-E-acryloyl]-benzoic acid
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCCCCCCC1(CCCCCCCC)c2ccccc2-c2ccc(C(=O)NNC(=O)c3cc(Cl)ccc3Cl)cc21
Reaction #11280
desired intermediate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1nc2ccc(N3CCCCC3)cc2c(-c2ccccc2)c1S(C)(=O)=O
Reaction #41934
solid
Ausbeute 398.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1nc2ccc(N3CCOCC3)cc2c(-c2ccccc2)c1S(C)(=O)=O
Reaction #41935
solid
Ausbeute 78.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1nc2ccc(N3CCCCC3)cc2c(N2CCOCC2)c1S(C)(=O)=O
Reaction #41939
solid
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1nc2ccc(N3CCOCC3)cc2c(-c2ccc(F)cc2)c1S(C)(=O)=O
Reaction #41946
solid
Ausbeute 408.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1nc2ccc(N3CCOCC3)cc2c(-c2ccc(Cl)cc2)c1S(C)(=O)=O
Reaction #41948
solid
Ausbeute 43.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1nc2ccc(N3CCOCC3)cc2c(-c2ccc(C(F)(F)F)cc2)c1S(C)(=O)=O
Reaction #41949
solid
Ausbeute 36.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1nc2ccc(N3CCOCC3)cc2c(-c2cc(F)c(F)cc2F)c1S(C)(=O)=O
Reaction #41950
solid
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(Nc1cccc2cc[nH]c12)OCc1ccccc1
Reaction #41976
title compound
Ausbeute 96.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)N1CCC(c2ccccc2Sc2ccc(C(F)(F)F)cc2)CC1
Reaction #43516
4-[2-(4-trifluoromethyl-phenylsulfanyl)-phenyl]-piperidine-1-carboxylic acid tert-butyl ester
Ausbeute 59.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(O)C(O)C12CC3CC(CC(C3)C1)C2
Reaction #46047
α-hydroxytricyclo[3.3.1.13,7]decane-1-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
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