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CC#N.ClC(Cl)(Cl)Cl.O

C[C@@H]1C[C@@H](C(=O)O)N(C(=O)OC(C)(C)C)C1=O
Reaction #2977
product
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCO/N=[N+](\[O-])N1CCC[C@H]1C(=O)O
Reaction #475395
title product
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-n2cc(C#N)c(C(F)(F)F)n2)cc1.c1coc(-c2ccn[nH]2)c1
Reaction #481995
title compound
Ausbeute 102.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C(F)(F)F)nn(-c2ccc(OC)cc2)c1C(=O)O
Reaction #481998
title compound
Ausbeute 53.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C(=O)O)C(F)(F)F
Reaction #560543
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(CC(=O)O)C[C@@H](C(=O)Nc2ccccc2)n2c1ncc(N(Cc1cccc(C(F)(F)F)c1)C(=O)OCc1ccccc1)c2=O
Reaction #568438
117b
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-n2nc(C(F)(F)F)c(C#N)c2C(=O)O)cc1
Reaction #697339
title compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C(F)(F)F)nn(-c2ccc(OC)cc2)c1C(=O)O
Reaction #697342
title compound
Ausbeute 53.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(C(=O)O)CC2CC21
Reaction #799989
title compound
Ausbeute 46.1%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CCOCN1C(=O)[C@@]2(c3ccc(Cl)cc31)[C@@H](c1cccc(Cl)c1)C[C@H](CC(=O)O)C(=O)N2CC1CC1
Reaction #1019128
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](CO[Si](c1ccccc1)(c1ccccc1)C(C)(C)C)N1C(=O)[C@H](CC(=O)O)C[C@H](c2cccc(Cl)c2)[C@H]1c1ccc(Cl)cc1
Reaction #1019247
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C(=O)O)C(F)(F)F
Reaction #1126862
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CCOCN1C(=O)[C@@]2(c3ccc(Cl)cc31)[C@@H](c1cccc(Cl)c1)C[C@H](CC(=O)O)C(=O)N2CC1CC1
Reaction #1135441
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](CO[Si](c1ccccc1)(c1ccccc1)C(C)(C)C)N1C(=O)[C@H](CC(=O)O)C[C@H](c2cccc(Cl)c2)[C@H]1c1ccc(Cl)cc1
Reaction #1135560
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CC(C)(C)c1cc(F)ccc1Br)C(=O)c1ccccc1
Reaction #1334740
product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C(N)=O)c1ccc(C(=O)O)cc1
Reaction #1351395
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc2c(c1)NC(=O)C1(F)CCCC21
Reaction #1457101
3a-Fluoro-1,2,3,3a,5,9b-hexahydrocyclopenta[c]quinolin-4-one-7-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CC(C)(C)c1cc(F)ccc1Br)C(=O)c1ccccc1
Reaction #1461802
product
DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H](C)[C@@H](C(=O)O)N(C)C(=O)OC(C)(C)C
Reaction #1605930
(2S,3R)-2-(tertbutoxycarbonyl-methyl-amino)-4-methoxy-3-methyl-butyric acid
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](COCC(C)(C)O)[C@@H](C(=O)O)N(C)C(=O)OC(C)(C)C
Reaction #1605935
compound 2.7c
Ausbeute 89.5%DOI: 10.6084/m9.figshare.5104873.v1
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