Teilstruktursuche

788860

Cc1cc(C23CCCN2CCC3)on1
Reaction #3379
oil
Ausbeute 11.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(N)CC1C(=O)O
Reaction #46102
4-amino-1-boc-pyrrolidine-2-carboxylic acid
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@]1(C)C[C@@H](O)CN1C(=O)OC(C)(C)C
Reaction #52157
N-BOC-4(R)-hydroxy-2-methyl-(L)-proline, methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
Br.O=C(O)C1NCC2CCCC21
Reaction #52161
3-azabicyclo[3.3.0]octane-2-carboxylic acid, hydrobromide
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](OCc2ccc(Br)cc2)C[C@@]1(C)C(=O)O
Reaction #78257
(2S,4R)-N-Boc-4-(4-bromo-benzyloxy)-2-methyl-proline
Ausbeute 28.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@]1(C)C[C@@H](OCc2ccc(Br)cc2)CN1
Reaction #78258
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1C(=O)N1C(c2ccco2)C(C(=O)O)CC1(Cc1c[nH]cn1)C(=O)O
Reaction #79444
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCN1CCC[C@H]1C(N)=O
Reaction #82335
N1 -isopentyl-L-prolinamide
Ausbeute 111.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N1C[C@H](N=[N+]=[N-])C[C@]1(C(N)=O)C(=O)OCc1ccccc1.N#N
Reaction #82388
N2 (benzyloxycarbonyl)-4(R)-azido-N1 -tert.butyl-L-prolinamide
Ausbeute 78.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N1C[C@H](N)C[C@]1(C(N)=O)C(=O)OCc1ccccc1.N#N
Reaction #82389
N2 (benzyloxycarbonyl)-4(R)-amino-N1 -tert-butyl-L-prolinamide
Ausbeute 56.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H]1C[C@@H](C(N)=O)N(C(C)(C)C)C1
Reaction #82390
4(R)-(tert.butoxyformamido)-N1 -tert.butyl-L-prolinamide
Ausbeute 106.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(C(=O)OCC)C2CCCC2CN1C(C)=O
Reaction #89137
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Br.O=C(O)C1NCC2CCCC21
Reaction #89138
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(C(=O)OCC)C2CCCC2CN1C(C)=O
Reaction #89271
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Br.O=C(O)C1NCC2CCCC21
Reaction #89272
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@]1(C)CC[C@H](c2cc(-c3ccc(F)cc3C)c(N(C)C(=O)C(C)(C)c3cc(C(F)(F)F)cc(C(F)(F)F)c3)cn2)N1
Reaction #156716
title compound
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@]1(C)CC[C@H](c2cc(-c3ccc(F)cc3C)c(N(C)C(=O)C(C)(C)c3cc(C(F)(F)F)cc(C(F)(F)F)c3)cn2)N1
Reaction #156717
title compound
Ausbeute 97.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@]1(C)CC[C@@H](c2cc(-c3ccc(F)cc3C)c(N(C)C(=O)C(C)(C)c3cc(C(F)(F)F)cc(C(F)(F)F)c3)cn2)N1
Reaction #156722
title compound
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)N1CCC[C@H]1[C@H](OC)[C@@H](C)C(=O)N[C@@H](Cc1ccccc1)C(=O)OC)OC)N(C)C(=O)[C@@H](NC(=O)[C@]1(C)CCCN1C(=O)OC(C)(C)C)C(C)C
Reaction #161955
#116
Ausbeute 75.1%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)N1CCC[C@H]1[C@H](OC)[C@@H](C)C(=O)N[C@@H](Cc1ccccc1)C(=O)OC)OC)N(C)C(=O)[C@@H](NC(=O)[C@@]1(C)CCCN1)C(C)C.O=C(O)C(F)(F)F
Reaction #161968
#131
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter