KHSO4

N=C(NC(=O)OCc1ccccc1)N1CCC(CCN)C1
Reaction #965
title compound
Ausbeute 67.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCN(C(=O)OC(C)(C)C)[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](CCSC)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)NCCCCCC(=O)OC.CCN(C(=O)OC(C)(C)C)[C@@H](Cc1ccc(O)cc1)C(=O)N[C@H](CCSC)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)NCCCCCC(=O)OC.Cl.Cl.O
Reaction #3884
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
—
Reaction #6965
compound 11A
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(NC1CC1)c1ccc(F)c(OCc2cnc(Nc3ccccn3)s2)c1
Reaction #6967
title compound
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)C(Cc1ccc2ccccc2c1)N1CCN(S(=O)(=O)c2ccccc2[N+](=O)[O-])C(CCCNC(=O)OCc2ccccc2)C1=O
Reaction #8624
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@@H](CS(=O)(=O)N(Cc1ccccc1)C(c1ccccc1)c1ccccc1)C(=O)O
Reaction #8933
3-[N-(benzyl)-N-(diphenylmethyl)aminosulfonyl]-2(R)-methylpropionic acid
Ausbeute 80.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@H](NC(=O)C(F)(F)F)[C@H](Oc1ccc2c(cnn2-c2cccc(CN3CCOCC3)c2)c1)c1ccccc1
Reaction #41461
2,2,2-trifluoro-N-((1R,2S)-1-(1-(3-(morpholinomethyl)phenyl)-1H-indazol-5-yloxy)-1-phenylpropan-2-yl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(C(=O)NC2CC2)cc1-c1cc2cnnc(Cl)c2s1
Reaction #47860
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Oc1ccnc(O)c1I
Reaction #47936
2,4-dihydroxy-3-iodopyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)C[C@@H](C=O)NC(=O)OC(C)(C)C
Reaction #50728
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
COC(=C1C(=O)Nc2ccc([N+](=O)[O-])cc21)c1ccc(OC)cc1
Reaction #53232
3-[1-methoxy-1-(4-methoxyphenyl)-methylidene]-5-nitro-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CN(C)CCSC[C@H]1CC[C@H](N(C)S(=O)(=O)c2ccc(C(F)(F)F)cc2)CC1
Reaction #53849
trans-N-[4-(2-Dimethylamino-ethylsulfanylmethyl)-cyclohexyl]-N-methyl-4-trifluoromethyl-benzenesulfonamide
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CON(C)C(=O)[C@H]1CC[C@H](N(C)C(=O)OC(C)(C)C)CC1
Reaction #53854
trans-[4-(Methoxy-methyl-carbamoyl)-cyclohexyl]-methyl-carbamic acid tert-butyl ester
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
—
Reaction #53855
12.83
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CN(C(=O)OC(C)(C)C)[C@H]1CC[C@H](/C=C/CO)CC1
Reaction #53918
trans-(1E)-[4-(3-Hydroxy-propenyl)-cyclohexyl]-methyl-carbamic acid tert-butyl ester
Ausbeute 79.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CN([C@H]1CC[C@H](OCCC(=O)O)CC1)S(=O)(=O)c1ccc(C(F)(F)F)cc1
Reaction #53943
trans-3-{4-[Methyl-(4-trifluoromethyl-benzenesulfonyl)-amino]-cyclohexyloxy}-propionic acid
Ausbeute 99.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CON(C)C(=O)CCCO[C@H]1CC[C@H](N(C)S(=O)(=O)c2ccc(C(F)(F)F)cc2)CC1
Reaction #53948
trans-N-Methoxy-N-methyl-4-{4-[methyl-(4-trifluoromethyl-benzenesulfonyl)-amino]-cyclohexyloxy}-butyramide
Ausbeute 94.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CO[C@H](COCc1ccc(/C=C/Cn2cccc2C(=O)c2ccc(C)cc2)cc1)C(=O)O
Reaction #59833
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)C[C@@H](C=O)NC(=O)OC(C)(C)C
Reaction #60572
Boc-Leucinal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)NC(=O)CC(CC1(C(=O)N[C@H]2CCc3ccccc3N(CC(=O)OC(C)(C)C)C2=O)CCCC1)C(=O)O
Reaction #60631
title compound
Ausbeute 88.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Seite 1Weiter