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CC(CN)O

COC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CCl
Reaction #1526
(2S,3S)-1-chloro-3-methoxycarbonylamino-4-phenyl-2-butanol
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@@H](Cc1ccccc1)[C@H](O)CCl
Reaction #1527
(2S,3S)-1-chloro-3-methoxycarbonylamino-4-phenyl-2-butanol
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O[Si](c1ccccc1)(c1ccccc1)C(C)(C)C)[C@H](NC(=O)OC(C)(C)C)c1cc(F)c(F)c(F)c1
Reaction #44607
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O[Si](c1ccccc1)(c1ccccc1)C(C)(C)C)[C@H](N)c1cc(F)c(F)c(F)c1
Reaction #44608
title compound
Ausbeute 91.1%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O[Si](c1ccccc1)(c1ccccc1)C(C)(C)C)[C@H](NC(=O)OC(C)(C)C)c1cc(F)c(F)c(F)c1
Reaction #44635
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O[Si](c1ccccc1)(c1ccccc1)C(C)(C)C)[C@H](N)c1cc(F)c(F)c(F)c1
Reaction #44636
title compound
Ausbeute 91.1%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12C[C@H](N3CCOCC3)[C@@H](O)C[C@@H]1CC[C@@H]1[C@@H]2CC[C@]2(C)[C@@H](C(=O)CBr)CC[C@@H]12
Reaction #64870
(2β,3α,5α)-21-bromo-3-hydroxy-2-(4-morpholinyl)pregnan-20-one
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(=O)N[C@@H](CC=O)CO[Si](C)(C)C(C)(C)C
Reaction #80532
residual brown liquid
Ausbeute 81.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](NC(=O)N(C)Cc1csc(N)n1)C(=O)N[C@@H](Cc1ccccc1)[C@H](O)[C@@H](O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)N(C)Cc1csc(N)n1)C(C)C
Reaction #81104
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](NC(=O)N(C)Cc1csc(N)n1)C(=O)N[C@@H](Cc1ccccc1)[C@H](O)[C@H](O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)N(C)Cc1csc(N)n1)C(C)C
Reaction #81105
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(CC(=O)O)CC(c2cccc(Cl)c2)C(c2ccc(Cl)cc2)N(C(C=O)CCC=O)C1=O
Reaction #197809
DOI: 10.1039/C8SC04228D
CCOc1ccccc1C1OC(=O)NC1=O
Reaction #198978
DOI: 10.1039/C8SC04228D
COC1CC(C(=O)O)N(C(=O)CCCS)C1
Reaction #206655
DOI: 10.1039/C8SC04228D
CC(C)(C)C(N)C(=O)N1CCC2C1C(Oc1ccc(F)c(F)c1)CN2C1CCOCC1
Reaction #207517
DOI: 10.1039/C8SC04228D
CC(=O)N1C=C(c2ccccc2)N(CC(=O)NC(Cc2ccccc2)C(=O)C2=NC(C)(C)CO2)C(=O)C1C(C)C
Reaction #210175
DOI: 10.1039/C8SC04228D
CC(=O)NC(Cc1cc(F)cc(F)c1)C(O)CNC1(c2cccc(Br)c2)CCC2(CC1)OCCO2
Reaction #219278
N-[3-[8-(3-Bromo-phenyl)-1,4-dioxa-spiro[4.5]dec-8-ylamino]-1-(3,5-difluoro-benzyl)-2-hydroxy-propyl]-acetamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC(Cc1cc(F)cc(F)c1)C(O)CNC1(c2cccc(Br)c2)CCC(=O)CC1
Reaction #219279
Compound 19
Ausbeute 100.7%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](C)[C@@]1(NC(C)=O)CCN([C@@H](CCc2ccccc2)C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@@H](Oc3ccccc3)CN2)C1=O
Reaction #220138
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](C)[C@@]1(NC(C)=O)CCN([C@@H](CCc2ccccc2)C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@@H](Oc3cccnc3)CN2)C1=O
Reaction #220143
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)N(CC(C)=Cc2ccccc2)CC2CC(O)CN2C2CCOCC2)cc2c1OC(C)(C)O2
Reaction #223215
DOI: 10.1039/C8SC04228D
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