Teilstruktursuche

CN(C)C(On1nnc2ccc(Cl)cc21)=[N+](C)C.F[P-](F)(F)(F)(F)F

—
Reaction #74192
material
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C2(NC(=O)c3cc(Cl)cnc3N3CC(COc4ccc(F)cc4)C3)CC2)cc1
Reaction #159689
title compound ( D163 )
Ausbeute 64.1%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #426000
material
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](OC(=O)OC1CCCCC1)OC(=O)[C@](C)(CO)C[C@@H](Cc1ccc(-c2ccccc2)cc1)NC(=O)c1cnn[nH]1
Reaction #535827
(2S,4R)-5-Biphenyl-4-yl-2-hydroxymethyl-2-methyl-4-[(3H-[1,2,3]triazole-4-carbonyl)-amino]-pentanoic acid (S)-1-cyclohexyloxycarbonyloxy-ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H](O)C[C@@H](Cc1ccc(Br)cc1)NC(=O)c1cn(O)nn1
Reaction #603620
title compound
Ausbeute 61.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(COc2cc(C(=O)N[C@H](Cc3ccc(-c4cccc(Cl)c4)cc3)C[C@@H](O)C(=O)O)nn2C)cc1
Reaction #603622
title compound
Ausbeute 70.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H](Cc1ccc(-c2cccc(Cl)c2)cc1)C[C@@H](O)C(=O)O)c1ccc2nnn(O)c2c1
Reaction #603626
title compound
Ausbeute 21.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1nc(C(=O)N[C@H](Cc2ccc(-c3cccc(Cl)c3)cc2)C[C@@H](O)C(=O)O)cc1O
Reaction #603637
title compound
Ausbeute 14.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H](Cc1ccc(-c2cccc(Cl)c2)cc1)C[C@@H](O)C(=O)O)c1cc(O)n(-c2ccccn2)n1
Reaction #603640
title compound
Ausbeute 58.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1oc(=O)oc1COC(=O)[C@H](O)C[C@@H](Cc1ccc(-c2cccc(Cl)c2)cc1)NC(=O)c1cc(O)n(-c2ccccn2)n1
Reaction #603641
title compound
Ausbeute 80.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)N[C@H](Cc2ccc(-c3cccc(Cl)c3)cc2)C[C@@H](O)C(=O)O)on1
Reaction #603648
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H](Cc1ccc(-c2cccc(Cl)c2)cc1)C[C@@H](O)C(=O)O)c1nn(-c2ccccc2)c(=O)[nH]1
Reaction #603657
title compound
Ausbeute 3.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](OC(=O)OC1CCCCC1)OC(=O)[C@](C)(CO)C[C@@H](Cc1ccc(-c2ccccc2)cc1)NC(=O)c1cnn[nH]1
Reaction #610610
(2S,4R)-5-Biphenyl-4-yl-2-hydroxymethyl-2-methyl-4-[(3H-[1,2,3]triazole-4-carbonyl)-amino]-pentanoic acid (S)-1-cyclohexyloxycarbonyloxy-ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](OC(=O)OC1CCCCC1)OC(=O)[C@](C)(CO)C[C@@H](Cc1ccc(-c2ccccc2)cc1)NC(=O)c1cnn[nH]1
Reaction #622384
(2S,4R)-5-Biphenyl-4-yl-2-hydroxymethyl-2-methyl-4-[(3H-[1,2,3]triazole-4-carbonyl)-amino]-pentanoic acid (S)-1-cyclohexyloxycarbonyloxy-ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NN(Cc1ccc(-c2cc(Cl)ccc2F)cc1)C[C@@H](O)C(=O)O)c1nn(-c2cccc(Cl)c2)c(=O)[nH]1
Reaction #628686
title compound
Ausbeute 46.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NN(Cc1ccc(-c2cc(Cl)ccc2F)cc1)C[C@@H](O)C(=O)O)c1cnc(O)s1
Reaction #628687
title compound
Ausbeute 15.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NN(Cc1ccc(-c2cc(Cl)ccc2F)cc1)C[C@@H](O)C(=O)O)c1nn(-c2ccccc2)c(=O)[nH]1
Reaction #628709
title compound
Ausbeute 75.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@H](O)CN(Cc1ccc(-c2cc(Cl)ccc2F)cc1)NC(=O)c1nn(-c2ccccc2)c(=O)[nH]1
Reaction #628711
title compound
Ausbeute 1.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)COC(=O)[C@H](O)CN(Cc1ccc(-c2cc(Cl)ccc2F)cc1)NC(=O)c1nn(-c2ccccc2)c(=O)[nH]1
Reaction #628712
title compound
Ausbeute 1.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc(C(=O)NN(Cc2ccc(-c3cc(Cl)ccc3F)cc2)C[C@@H](O)C(=O)O)[nH]n1
Reaction #628719
title compound
Ausbeute 57.9%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter