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10681

COc1ccc(CSC[C@@H]2CCCN2C(=O)OC(C)(C)C)cc1
Reaction #5203
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC1COc1ccc(OCc2ccccc2)cc1
Reaction #41200
crystals
Ausbeute 55.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@H]1COC1Cc2ccccc2C1
Reaction #57344
indanyl ether
Ausbeute 17.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OC[C@@H]2CCCN2C(=O)OC(C)(C)C)cc1
Reaction #73860
title compound
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@@H](F)C[C@@H]1COS(C)(=O)=O
Reaction #168575
tert-butyl (2R,4S)-4-fluoro-2-methanesulfonyloxymethylpyrrolidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(O[Si](C)(C)C(C)(C)C)CC1CC#N
Reaction #186246
DOI: 10.1039/C8SC04228D
C[SiH](C)OC1(CSc2ccc(S(N)(=O)=O)cc2)CC(C(C)(C)C)CN1C(=O)OC(C)(C)C
Reaction #191584
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCCC1COc1ccc(NCc2ccccc2)cc1
Reaction #193202
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCCC1CF
Reaction #203127
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CC(O[Si](C)(C)C(C)(C)C)CC1COS(C)(=O)=O
Reaction #211605
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCCC1COc1ccc(C(=O)c2ccc(I)cc2)cc1
Reaction #213649
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCCC1CSc1ccc(I)cc1
Reaction #222320
DOI: 10.1039/C8SC04228D
COCC1CC(NC(=O)c2ccc(Cl)s2)CN1C(=O)OC(C)(C)C
Reaction #242881
DOI: 10.1039/C8SC04228D
CNCC1CC(Oc2cc(F)cc([N+](=O)[O-])c2)CN1C(=O)OC(C)(C)C
Reaction #252437
DOI: 10.1039/C8SC04228D
CC1CCCN1C(=O)OC(C)(C)C
Reaction #254332
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1C2CC(CC2N2CCCC2)C1C(=O)N1CCCC1C#N
Reaction #258844
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CC(Cc2ccc(Cl)c(Cl)c2)CC1COS(C)(=O)=O
Reaction #262970
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CC(NC(=O)c2ccc(Cl)s2)CC1CF
Reaction #278804
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCCC1COc1ccc2c(Nc3cnn(CC(=O)Nc4cccc(F)c4)c3)ncnc2c1
Reaction #282014
DOI: 10.1039/C8SC04228D
Cc1ccc(S(=O)(=O)OCC2CCCN2C(=O)OC(C)(C)C)cc1
Reaction #291237
DOI: 10.1039/C8SC04228D
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