Teilstruktursuche

1016380

COCCOC(=O)OCCOC
Reaction #335842
bis(2-methoxyethyl)carbonate
Ausbeute 87.5%DOI: 10.6084/m9.figshare.5104873.v1
COCCOC(=O)OCCOC
Reaction #460851
bis(2-methoxyethyl)carbonate
Ausbeute 87.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)OC[C@H]1O[C@@H](n2cnc3c(=O)[nH]c(N)nc32)C[C@@H]1F)COC(=O)[C@@H](N)C(C)C
Reaction #576252
titled product
DOI: 10.6084/m9.figshare.5104873.v1
COC1C2OC(=O)OC2C(Oc2ccc3cc(NC(C)=O)c(=O)oc3c2)OC1(C)C
Reaction #750970
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)OC[C@H]1O[C@@H](n2cnc3c(=O)[nH]c(N)nc32)C[C@@H]1F)COC(=O)[C@@H](N)C(C)C
Reaction #1077181
titled product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCCOCCOCCOCCOCCOCCOCc1ccccc1)OCC1CN(c2ccc3cc(-c4ccccc4C(F)(F)F)[nH]c(=O)c3c2)C(=O)O1
Reaction #1215628
DOI: 10.1039/C8SC04228D
O=C(OCCOCCOCCOCCOCCOCCOCc1ccccc1)OC[C@@H]1CN(c2ccc3cc(-c4ccccc4C(F)(F)F)[nH]c(=O)c3c2)C(=O)O1
Reaction #1250136
2-[2-(2-{2-[2-(2-benzyloxyethoxy)ethoxy]ethoxy}ethoxy)ethoxy]ethyl carbonate (S)-2-oxo-3-[1-oxo-3-(2-trifluoromethylphenyl)-1,2-dihydroisoquinolin-7-yl]-oxazolidin-5-ylmethyl ester
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC(=O)OC(COC(=O)OC[C@H]1O[C@@H](n2cnc3c(=O)[nH]c(N)nc32)C[C@@H]1F)COC(=O)[C@@H](N)C(C)C
Reaction #1257842
titled product
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1[C@H]2OC(=O)O[C@H]2[C@H](Oc2ccc3cc(NC(C)=O)c(=O)oc3c2)OC1(C)C
Reaction #1524180
N-(7-((3aR,4R,7R,7aR)-7-methoxy-6,6-dimethyl-2-oxo-tetrahydro-3aH-[1,3]dioxolo[4,5-c]pyran-4-yloxy)-2-oxo-2H-chromen-3-yl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1[C@H]2OC(=O)O[C@H]2[C@H](Oc2ccc3cc(NC(C)=O)c(=O)oc3c2)OC1(C)C
Reaction #1598386
N-(7-((3aR,4R,7R,7aR)-7-methoxy-6,6-dimethyl-2-oxo-tetrahydro-3aH-[1,3]dioxolo[4,5-c]pyran-4-yloxy)-2-oxo-2H-chromen-3-yl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2cc(NC(=O)OCc3ccccc3)c(=O)oc2c(C)c1O[C@@H]1OC(C)(C)[C@H](OC)[C@H]2OC(=O)O[C@@H]12
Reaction #1598412
25a
Ausbeute 95.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1cc2cc(NC(=O)OCc3ccccc3)c(=O)oc2c(C)c1O[C@@H]1OC(C)(C)[C@H](OC)[C@H]2OC(=O)O[C@@H]12
Reaction #1598413
25b
Ausbeute 95.8%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1[C@H]2OC(=O)O[C@H]2[C@H](Oc2c(OC(C)C)cc3cc(NC(=O)OCc4ccccc4)c(=O)oc3c2C)OC1(C)C
Reaction #1598414
25c
Ausbeute 95.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(O[C@@H]2OC(C)(C)[C@H](OC)[C@H]3OC(=O)O[C@@H]23)c(C)c2oc(=O)c(NC(=O)OCc3ccccc3)cc12
Reaction #1598415
25d
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1[C@H]2OC(=O)O[C@H]2[C@H](Oc2ccc3cc(NC(=O)OCc4ccccc4)c(=O)oc3c2Cc2ccccc2)OC1(C)C
Reaction #1598416
25e
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1[C@H]2OC(=O)O[C@H]2[C@H](Oc2ccc3cc(NC(=O)OCc4ccccc4)c(=O)oc3c2-c2ccccc2)OC1(C)C
Reaction #1598417
25f
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1c(O[C@@H]2OC(C)(C)[C@H](OC)[C@H]3OC(=O)O[C@@H]23)ccc2cc(NC(=O)OCc3ccccc3)c(=O)oc12
Reaction #1598418
25h
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2cc(C(=O)Nc3cc4cc(OC)c(O[C@@H]5OC(C)(C)[C@H](OC)[C@@H](O)[C@H]5O)c(C)c4oc3=O)ccc2OC)c1
Reaction #1598419
26a
Ausbeute 3.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1cc2cc(NC(=O)c3ccc(OC)c(-c4cccc(OC)c4)c3)c(=O)oc2c(C)c1O[C@@H]1OC(C)(C)[C@H](OC)[C@@H](O)[C@H]1O
Reaction #1598420
26b
Ausbeute 7.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2cc(C(=O)Nc3cc4cc(OC(C)C)c(O[C@@H]5OC(C)(C)[C@H](OC)[C@@H](O)[C@H]5O)c(C)c4oc3=O)ccc2OC)c1
Reaction #1598421
26c
Ausbeute 14.6%DOI: 10.6084/m9.figshare.5104873.v1
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