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417758

CC(C)(C)c1cn(C[C@H]2CCCO2)/c(=N/C(=O)c2cc(C(F)(F)F)ccc2O[C@@H]2CCNC2)s1
Reaction #165732
title compound
Ausbeute 90.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Oc2ccccc2C=O)C1
Reaction #172297
tert-butyl 3-(2-formylphenoxy)pyrrolidine-1-carboxylate
Ausbeute 23.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Oc2ccccc2-c2nc3c(C(=O)O)cccc3[nH]2)C1
Reaction #172298
titled compound 31
Ausbeute 84.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Oc2ccc(Cl)cc2O)C1
Reaction #324439
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(Oc2cc(F)ccc2OCc2cccc(Cl)c2)C1
Reaction #324462
solid
Ausbeute 124.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)/C=C/c1ccc2c(c1)C(=O)CC1(CCNC1)O2
Reaction #961404
(±)-(E)-3-[4-oxo-spiro(chromane-2,3′-pyrrolidine)-6-yl]-acrylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC2(CC(=O)c3cc(/C=C/C(=O)NOC4CCCCO4)ccc3O2)C1
Reaction #961412
(±)-(E)-3-[1′-tert-butoxycarbonyl-4-oxo-spiro(chromane-2,3′-pyrrolidine)-6-yl]-N-(tetrahydro-pyran-2-yloxy)-acrylamide
Ausbeute 81.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Oc2ccc(Br)cc2C=O)C1
Reaction #1182272
(R/S)-3-(4-bromo-2-formyl-phenoxy)-pyrrolidine-1-carboxylic acid tert-butyl ester
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(N=Cc1cc(Br)ccc1OC1CCN(C(=O)OC(C)(C)C)C1)O[Si](C)(C)C
Reaction #1182273
(R/S)-1-[5-bromo-2-(1-tert-butoxycarbonyl-3-pyrrolidinyloxy)-phenyl]-3-trimethylsilyoxy-2-aza-1,3-butadiene
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Oc2ccc(I)cc2C=O)C1
Reaction #1182275
(R/S)-3-(2-formyl-4-iodo-phenoxy)-pyrrolidine-1-carboxylic acid tert-butyl ester
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(N=Cc1cc(I)ccc1OC1CCN(C(=O)OC(C)(C)C)C1)O[Si](C)(C)C
Reaction #1182276
(R/S)-1-[2-(1-tert-butoxycarbonyl-3-pyrrolidinyloxy)-5-iodo-phenyl]-3-trimethylsilyoxy-2-aza-1,3-butadiene
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Oc2ccccc2C=O)(C(F)(F)F)C1
Reaction #1566233
title compound
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Oc2ccccc2C(=O)O)(C(F)(F)F)C1
Reaction #1566234
title compound
Ausbeute 102.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2c3c(nn2c(C)c1Cl)CN(C(=O)c1ccc(F)cc1O[C@@H]1CCNC1)C3
Reaction #1566246
title compound
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2c3c(nn2c(C)c1Cl)CN(C(=O)c1ccc(F)cc1O[C@H]1CCNC1)C3.O=CO
Reaction #1566248
title compound
Ausbeute 4.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc2c3c(nn2c(C)c1Cl)CN(C(=O)c1ccccc1OC1(C(F)(F)F)CCNC1)C3
Reaction #1566295
title compound
Ausbeute 25.0%DOI: 10.6084/m9.figshare.5104873.v1