Teilstruktursuche

378202

CC(C)[C@H]1COC(=O)N1C(=O)[C@H](Cc1ccccc1)[C@@H](O)c1ccccc1
Reaction #5037
(4S)-3-[(2R)-2-Benzyl-(3R)-3-hydroxy-3-phenylpropionyl]-4-(2-propyl)-oxazolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@@H]1NC(=O)OC1=O
Reaction #54130
(S)-4-Isopropyl-oxazolidine-2,5-dione
Ausbeute 47.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](NC(=O)OCc1nc(C(C)C)cs1)C(C)C
Reaction #80991
desired compound
Ausbeute 52.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@@H](C(=O)O)[C@H](N)C(=O)O
Reaction #83740
2(S)-amino-3(S)-carboxy-4(R)-hydroxypentanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(=O)O)[C@H]1COC(=O)N1
Reaction #85653
(R)-2-((S)-2-oxooxazolidin-4-yl)propanoic acid
Ausbeute 92.1%DOI: 10.6084/m9.figshare.5104873.v1
CON(C)C(=O)[C@H](C)[C@H]1COC(=O)N1
Reaction #85654
(R)—N-methoxy-N-methyl-2-((S)-2-oxooxazolidin-4-yl)propanamide
Ausbeute 195.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CCCN(C(=O)OCc2ccccc2)[C@@H]1CO
Reaction #89164
title compound
Ausbeute 92.3%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #93638
B7
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H]1COC(=O)N1C(=O)CCC(F)(F)F
Reaction #155533
oil
Ausbeute 40.7%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc([C@H]2C[C@H]3CSC(NC(=O)c4ccccc4)=N[C@@]3(c3cc(C#N)ccc3F)CO2)cn1
Reaction #155610
N-[(4aR,6R,8aS)-8a-(5-cyano-2-fluorophenyl)-6-(1-methyl-1H-pyrazol-4-yl)-4,4a,5,6,8,8a-hexahydropyrano[3,4-d][1,3]thiazin-2-yl]benzamide
DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc([C@H]2C[C@H]3CSC(N)=N[C@@]3(c3cc(C#N)ccc3F)CO2)cn1
Reaction #155611
product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(=S)N[C@@]1(c2cc(Br)ccc2F)CO[C@@H](C2CC2)C[C@H]1CO)c1ccccc1
Reaction #155616
product
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(F)c([C@]23CO[C@@H](C4CC4)C[C@H]2CSC(NC(=O)c2ccccc2)=N3)c1
Reaction #155617
product
DOI: 10.6084/m9.figshare.5104873.v1
COC[C@@H](C)NCc1ccc(F)c([C@]23CO[C@@H](c4cnn(C)c4)C[C@H]2CSC(N)=N3)c1
Reaction #155619
product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(NC(=O)OC(C)(C)C)C(=O)Oc1ccc(C2(c3ccccc3)CCCCC2)cc1
Reaction #157911
tert-Butyl 1-((4-(1-phenylcyclohexyl)phenoxy)carbonyl)-2-methylpropylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(N)C(=O)Oc1ccc(C2(c3ccccc3)CCCCC2)cc1
Reaction #157912
4-(1-Phenylcyclohexyl)phenyl 2-amino-3-methylbutanoate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1C(O)CC(O)(C(=O)OCc2ccccc2)OC1C(O)C(O)COC(=O)C(NC(=O)OCc1ccccc1)C(C)C
Reaction #164435
( 1-5 )
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCCCCCN(NC(=O)OC(C)(C)C)C(=O)N1CC(Oc2cc(-c3ccccc3)nc3cc(OC)ccc23)CC1C(=O)NC1(C(=O)OCC)CC1C=C
Reaction #182583
DOI: 10.1039/C8SC04228D
CC(C)(CC1NC(C(=O)O)C(c2cccc(Cl)c2F)C1(C#N)c1ccc(Cl)cc1F)C1CC1
Reaction #187098
DOI: 10.1039/C8SC04228D
Cc1cc(Nc2nc(Cl)cn(C(CO)C3CC3)c2=O)c(C)nc1OC(F)F
Reaction #187414
DOI: 10.1039/C8SC04228D
Seite 1Weiter