Teilstruktursuche

1430261

CC1(C)CC(c2ccc(OS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)cc2N2CCN(C(=O)OC(C)(C)C)CC2)CC(C)(C)C1
Reaction #60481
title compound
Ausbeute 95.8%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F.O=S(=O)(O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F.Oc1ccc2ccccc2c1-c1cccc2ccccc12
Reaction #78429
Racemic Binaphthol Dinonaflate
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC[C@H](CF)N1c1ccnc(F)n1
Reaction #85639
(R)-4-(fluoromethyl)-3-(2-fluoropyrimidin-4-yl)oxazolidin-2-one
Ausbeute 40.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](F)[C@H]1COC(=O)N1c1ccnc(F)n1
Reaction #85642
(R)-4-((R)-1-fluoroethyl)-3-(2-fluoropyrimidin-4-yl)oxazolidin-2-one
Ausbeute 28.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](F)[C@H]1COC(=O)N1c1nc(F)ncc1F
Reaction #85646
(R)-3-(2,5-difluoropyrimidin-4-yl)-4-((R)-1-fluoroethyl)oxazolidin-2-one
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](F)[C@H]1COC(=O)N1c1ccnc(F)n1
Reaction #85648
(R)-4-((S)-1-fluoroethyl)-3-(2-fluoropyrimidin-4-yl)oxazolidin-2-one
Ausbeute 14.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)OC[C@@H]2[C@H](C)F)cc1
Reaction #85759
desired product
Ausbeute 95.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](F)[C@H]1COC(=O)N1c1nc(F)ncc1F
Reaction #85761
(R)-3-(2,5-difluoropyrimidin-4-yl)-4-((S)-1-fluoroethyl)oxazolidin-2-one
Ausbeute 47.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)OC[C@@H]2[C@H](C)F)cc1
Reaction #85784
(R)-4-((S)-1-fluoroethyl)-3-(4-methoxybenzyl)oxazolidin-2-one
Ausbeute 95.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1=N[C@@]2(c3ccc(F)cc3F)CO[C@H](CF)[C@H]2CS1)c1ccccc1
Reaction #155558
title compound
Ausbeute 65.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1C[C@@H](CF)CN(C(=O)OCc2ccccc2)C1
Reaction #157172
cis (+/−)-benzyl 3-(tert-butoxycarbonylamino)-5-(fluoromethyl)piperidine-1-carboxylate
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1C[C@@H](CF)CN(C(=O)OCc2ccccc2)C1
Reaction #160731
cis (+/−)-benzyl 3-(tert-butoxycarbonylamino)-5-(fluoromethyl)piperidine-1-carboxylate
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)NC1Cc2cc(F)c(OS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)cc2C1Cc1ccccc1
Reaction #170079
3-benzyl-2-(ethoxycarbonylamino)-6-fluoro-2,3-dihydro-1H-inden-5-yl 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate
DOI: 10.6084/m9.figshare.5104873.v1
C=CC1CN(C(=O)OCc2ccccc2)CC1F
Reaction #179980
DOI: 10.1039/C8SC04228D
CC(C)(O)C#Cc1cnc2c(c1)C1(COC(N)=N1)c1cc(OS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)ccc1O2
Reaction #201421
DOI: 10.1039/C8SC04228D
Cn1nc(Br)cc1OS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F
Reaction #204958
DOI: 10.1039/C8SC04228D
CCOC(=O)c1sc2ccncc2c1OS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F
Reaction #205764
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(OS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)c2cnccc2n1C
Reaction #280043
DOI: 10.1039/C8SC04228D
COc1ccc2ccc(OS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)c(-c3nnc(OC(C)c4ccccc4)c4ccccc34)c2c1
Reaction #381117
DOI: 10.1039/C8SC04228D
COC(C)(C)C#Cc1cnc2c(c1)[C@@]1(COC(N)=N1)c1cc(OS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F)ccc1O2
Reaction #422941
(R)-2′-amino-3-(3-methoxy-3-methylbut-1-ynyl)-5′H-spiro[chromeno[2,3-b]pyridine-5,4′-oxazole]-7-yl 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter