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1345263

O[C@@H]1COC[C@H]1NCc1ccccc1
Reaction #168346
trans-4-(benzylamino) tetrahydrofuran-3-ol
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCl)N(Cc1ccccc1)[C@@H]1COC[C@H]1O
Reaction #168347
trans-N-benzyl-2-chloro-N-(4-hydroxytetrahydrofuran-3-yl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CO[C@@H]2COC[C@H]2N1Cc1ccccc1
Reaction #168348
trans-4-benzyltetrahydro-2H-furo[3,4-b][1,4]oxazin-3(4H)-one
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(CN2CCO[C@@H]3COC[C@H]32)cc1
Reaction #168349
trans-4-benzylhexahydro-2H-furo[3,4-b][1,4]oxazine
DOI: 10.6084/m9.figshare.5104873.v1
C1CO[C@@H]2COC[C@H]2N1
Reaction #168350
(trans)-hexahydro-2H-furo[3,4-b][1,4]oxazine
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1cccc(O)c1
Reaction #995728
3-hydroxybenzamide
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](c1ccccc1)N1C(=O)COC2COCC21
Reaction #1132885
(3aRS,7aSR)-7-((1R)-1-Phenyl-ethyl)-tetrahydro-2,4-dioxa-7-aza-inden-6-one
Ausbeute 64.1%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](c1ccccc1)N1CCO[C@@H]2COC[C@H]21
Reaction #1132886
(3aS,7aR)-7-((1R)-1-phenyl-ethyl)-hexahydro-2,4-dioxa-7-aza-indene
DOI: 10.6084/m9.figshare.5104873.v1
C1CO[C@@H]2COC[C@H]2N1.Cl
Reaction #1132887
(3aS,7aR)-Hexahydro-2,4-dioxa-7-aza-indene Hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CN(Cc1ccccc1)C1COC2C(OCc3ccccc3)COC21
Reaction #1141093
title compound
Ausbeute 46.4%DOI: 10.6084/m9.figshare.5104873.v1
CNC1COC2C(O)COC12
Reaction #1141094
title compound
Ausbeute 88.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1C1COC2C(O)COC21
Reaction #1141120
title compound
Ausbeute 25.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)OC1COC2C1OCC2N1C(=O)c2ccccc2C1=O
Reaction #1141121
title compound
Ausbeute 77.9%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NC1COC2C1OCC2N1C(=O)c2ccccc2C1=O
Reaction #1141122
crude product
DOI: 10.6084/m9.figshare.5104873.v1
NC1COC2C1OCC2N1C(=O)c2ccccc2C1=O
Reaction #1141123
crude product
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1C1COC2C(Nc3nc(Cl)ncc3Cl)COC21
Reaction #1141124
desired compound
Ausbeute 13.5%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(Nc2ncc(Cl)c(NC3COC4C3OCC4N3C(=O)c4ccccc4C3=O)n2)cn1
Reaction #1141125
title compound
Ausbeute 33.1%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(Nc2ncc(Cl)c(NC3COC4C(N)COC34)n2)cn1
Reaction #1141126
product
Ausbeute 63.7%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](Oc1ccc(C(=O)C2CC2)cc1)c1nc(-c2ccc(C(=O)N[C@@H]3C(=O)OC[C@H]3O)c(F)c2)no1
Reaction #1557052
title compound
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](Oc1ccc(C(=O)C2CC2)cc1)c1nc(-c2ccc(C(=O)N[C@@H]3C(=O)OC[C@@H]3O)c(F)c2)no1
Reaction #1557053
title compound
Ausbeute 18.0%DOI: 10.6084/m9.figshare.5104873.v1
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