Methanesulfonic acid

N[C@@H]1c2ccccc2C[C@@H]1O
Reaction #1274
cis 1-amino-2-indanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1CCCc2ccccc2N1
Reaction #1829
product
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1ccc(/C=C/c2cccc[c]2[Na])c(S(=O)(=O)O)c1
Reaction #2074
white powder
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1c(-c2cccc(OCC(O)CO)c2)oc2ccccc12
Reaction #2076
2-[3-(2,3-dihydroxypropoxy)phenyl]-3-methylbenzofuran
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1cc(C2C=CCC2)c(S(C)(=O)=O)cc1C(=O)N=C(N)N
Reaction #2989
N-diaminomethylene-2-methyl-4-(1-cyclopenten-3-yl)-5-methylsulfonylbenzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2C3=CC=C4CC(O)C=C[C@]4(C)[C@H]3CC[C@]12C
Reaction #4082
cholesta-1,5,7-trien-3-ol
Ausbeute 61.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCC1CN(c2ccc(F)c(C(F)(F)F)c2)C(c2cccc(Cl)c2)O1
Reaction #4218
2-m-Chlorophenyl-3-(3-trifluoromethyl-4-fluorophenyl)-5-ethyl oxazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCC1CN(c2ccc(Cl)c(C(F)(F)F)c2)C(c2cccc(C#N)c2)O1
Reaction #4219
2-m-Cyanophenyl-3-(3-trifluoromethyl-4-chlorophenyl)-5-ethyl oxazolidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CN1C[C@H](CCCl)Oc2ncccc2C1=O.Cl
Reaction #4918
(S)-2-(2-Chloroethyl)2,3-dihydro-4-methylpyrido[3,2-f][1,4]oxazepin-5(4H)-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CN1C[C@@H](CCCl)Oc2ncccc2C1=O.Cl
Reaction #4919
(R)-2-(2-Chloroethyl)-2,3-dihydro-4-methylpyrido[3,2-f]-1,4-oxazepin-5-(4H)-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
COc1ccc2c(c1)-c1cc(OC)ccc1C2=O
Reaction #5394
3,6-dimethoxy-9-fluorenone
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOC(=O)C1CCCCCCCC(=O)N1
Reaction #5486
ethyl 2-oxo-1-azacyclodecane-10-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)NCC1OC(=O)N2c3ccc(C(C)=O)cc3CC12
Reaction #6328
material
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)NCC1OC(=O)N2c3ccc(C(C)=O)cc3CC12
Reaction #6329
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)NCC1OC(=O)N2c3ccc(C(C)=O)cc3CC12
Reaction #6330
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCOC(=O)C1CCNC(=O)CC1
Reaction #7496
ester
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1ccc(CC(=O)c2sc(-c3ccc(C(F)(F)F)cc3)cc2C)cc1C
Reaction #9763
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)C[C@H]1C[C@@H](COC(=O)c2ccccc2)OC(C)(C)O1
Reaction #10241
2-[(4R,6S)-2,2-dimethyl-6-benzoyloxymethyl-1,3-dioxan-4-yl]acetic tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=Cc1nc2cc(Br)ccc2o1
Reaction #10501
5-bromo-2-vinyl-benzooxazole
Ausbeute 45.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C[C@@H]1CCCN1CCc1nc2cc(Br)ccc2[nH]1
Reaction #10512
title compound
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
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