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C(C(CO)N)O

COC1O[C@H]2[C@H](OCc3ccccc3)[C@@H]1N(C(=O)OCc1ccccc1)C[C@@H]2OCc1ccccc1
Reaction #6528
Methyl N-benzyloxycarbonyl-3,5-di-O-benzyl-2,6-dideoxy-2,6-imino-L-gulofuranoside
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(CC1CC1)C[C@@H](OC[C@@H](NC(=O)OCc1ccccc1)C(=O)O)c1ccccc1
Reaction #48402
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCC[C@@]1(C(=O)OC)CO[C@H](C(C)(C)C)N1C=O
Reaction #48542
title compound
Выход 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(C(=O)OC(C)(C)C)[C@@H](CO)CO1
Reaction #48618
desired compound
Выход 92.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1[C@@H]([C@@H](O)[C@@H](N)Cc2cccc(O)c2)COC1(C)C
Reaction #48626
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #48627
residue
Выход 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1cccc(O)c1)[C@H](O)C1CO[C@@H](OCC(C)(C)C)[C@H](C)N1C(=O)OC(C)(C)C
Reaction #48630
desired compound
Выход 34.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1cccc(C[C@H](NC(C)=O)[C@H](O)[C@H]2CO[C@@H](OCC(C)(C)C)[C@H](C)N2C(=O)OC(C)(C)C)c1
Reaction #48631
title compound
Выход 102.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@H](Cc1cc(F)cc(F)c1)[C@@H](O)[C@@H]1CO[C@@H](CCC(C)C)CN1C(=O)OC(C)(C)C
Reaction #48635
5-(S)-[2-(R)-Acetylamino-3-(3,5-difluorophenyl)-1-(R)-hydroxypropyl]-2-(S)-(3-methylbutyl)-morpholine-4-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1cc(F)cc(Cl)c1)[C@H](O)[C@H]1CO[C@@H](OCC(C)(C)C)CN1C(=O)OC(C)(C)C
Reaction #48641
title compound
Выход 45.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](CCC2CCCCC2)OC[C@@H]1[C@@H](O)[C@@H](N)Cc1cc(F)cc(F)c1
Reaction #48643
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1cc(F)cc(F)c1)[C@H](O)[C@H]1CO[C@@H](CCC2CCCCC2)CN1C(=O)OC(C)(C)C
Reaction #48644
title compound
Выход 37.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](CCC2CCCCC2)OC[C@@H]1CO
Reaction #48646
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1ccccc1)[C@H](O)[C@H]1CO[C@@H](CCC2CCCCC2)CN1C(=O)OC(C)(C)C
Reaction #48650
title compound
Выход 54.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1cc(F)cc(F)c1)[C@H](O)[C@H]1CO[C@@H](CO)CN1C(=O)OC(C)(C)C
Reaction #48657
title compound
Выход 68.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](COC2CCCCC2)OC[C@@H]1[C@@H](O)[C@@H](N)Cc1cc(F)cc(F)c1
Reaction #48660
desired compound
Выход 97.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)/C=C(\C)C(=O)N[C@@H](Cc1cc(F)cc(F)c1)[C@H](O)[C@H]1CO[C@@H](COC2CCCCC2)CN1C(=O)OC(C)(C)C
Reaction #48661
title compound
Выход 45.2%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@H]1CN(C(=O)OC(C)(C)C)C([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(C)=O)CO1
Reaction #48671
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1N[C@@H]([C@H](OCc2ccccc2)[C@H](Cc2cc(F)cc(F)c2)N(Cc2ccccc2)Cc2ccccc2)COC1O
Reaction #48692
desired compound
Выход 99.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1N[C@@H]([C@H](OCc2ccccc2)[C@H](Cc2cc(F)cc(F)c2)N(Cc2ccccc2)Cc2ccccc2)CO[C@H]1OCC(C)(C)C
Reaction #48693
desired compound
Выход 56.0%DOI: 10.6084/m9.figshare.5104873.v1
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