部分構造検索

426154

CC(C)(C)OC(=O)N1C(=O)O[C@H]2CCN(c3ccncc3N)C[C@H]21
Reaction #157181
(3aR,7aS)-tert-butyl 5-(3-aminopyridin-4-yl)-2-oxohexahydrooxazolo[4,5-c]pyridine-3(2H)-carboxylate
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(=O)O[C@H]2CCN(c3ccncc3NC(=O)c3nc(-c4c(F)cccc4F)ccc3N)C[C@H]21
Reaction #157182
(3aR,7aS)-tert-butyl 5-(3-(3-amino-6-(2,6-difluorophenyl)picolinamido)-pyridin-4-yl)-2-oxohexahydrooxazolo[4,5-c]pyridine-3(2H)-carboxylate
収率 46.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NC(=O)c1ccc(F)c(-c2ccc(N)c(C(=O)Nc3cnccc3N3CC[C@@H]4OC(=O)N(C(=O)OC(C)(C)C)[C@@H]4C3)n2)c1
Reaction #157183
(3aR,7aS)-tert-butyl 5-(3-(3-amino-6-(2-fluoro-5-(isopropylcarbamoyl)phenyl)picolinamido)pyridin-4-yl)-2-oxohexahydro-oxazolo[4,5-c]pyridine-3(2H)-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(=O)O[C@H]2CCN(c3ccncc3[N+](=O)[O-])C[C@H]21
Reaction #160736
(3aR,7aS)-tert-butyl 5-(3-nitropyridin-4-yl)-2-oxohexahydrooxazolo[4,5-c]pyridine-3(2H)-carboxylate
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(=O)O[C@H]2CCN(c3ccncc3N)C[C@H]21
Reaction #160737
(3aR,7aS)-tert-butyl 5-(3-aminopyridin-4-yl)-2-oxohexahydrooxazolo[4,5-c]pyridine-3(2H)-carboxylate
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(c2ccncc2N)C[C@@H]2[C@H]1OC(=O)N2C(=O)OC(C)(C)C
Reaction #160776
(3aR,7R,7aS)-tert-butyl 5-(3-aminopyridin-4-yl)-7-methyl-2-oxohexahydrooxazolo[4,5-c]pyridine-3(2H)-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CN(c2ccncc2N)C[C@@H]2[C@@H]1OC(=O)N2C(=O)OC(C)(C)C
Reaction #160778
(3aR,7S,7aR)-tert-butyl 5-(3-aminopyridin-4-yl)-7-methyl-2-oxohexahydrooxazolo[4,5-c]pyridine-3(2H)-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(=O)O[C@H]2CCN(c3ccncc3[N+](=O)[O-])C[C@H]21
Reaction #495637
(3aR,7aS)-tert-butyl 5-(3-nitropyridin-4-yl)-2-oxohexahydrooxazolo[4,5-c]pyridine-3(2H)-carboxylate
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CN(c2ccncc2N)CC2C1OC(=O)N2C(=O)OC(C)(C)C
Reaction #1230562
DOI: 10.1039/C8SC04228D
C[C@@H]1CN(c2ccncc2N)C[C@@H]2[C@H]1OC(=O)N2C(=O)OC(C)(C)C
Reaction #1610654
(3aR,7R,7aS)-tert-butyl 5-(3-aminopyridin-4-yl)-7-methyl-2-oxohexahydrooxazolo[4,5-c]pyridine-3 (2H)-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CN(c2ccncc2N)C[C@@H]2[C@@H]1OC(=O)N2C(=O)OC(C)(C)C
Reaction #1610656
(3aR,7S,7aR)-tert-butyl 5-(3-aminopyridin-4-yl)-7-methyl-2-oxohexahydrooxazolo[4,5-c]pyridine-3(2H)-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(=O)OC2CCN(c3ccncc3N)CC21
Reaction #1641459
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1C(=O)O[C@H]2CCN(c3ccncc3[N+](=O)[O-])C[C@H]21
Reaction #2007373
(3aR,7aS)-tert-butyl 5-(3-nitropyridin-4-yl)-2-oxohexahydrooxazolo[4,5-c]pyridine-3(2H)-carboxylate
収率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C(=O)O[C@H]2CCN(c3ccncc3N)C[C@H]21
Reaction #2007374
(3aR,7aS)-tert-butyl 5-(3-aminopyridin-4-yl)-2-oxohexahydrooxazolo[4,5-c]pyridine-3(2H)-carboxylate
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(c2ccncc2N)C[C@@H]2[C@H]1OC(=O)N2C(=O)OC(C)(C)C
Reaction #2007414
(3aR,7R,7aS)-tert-butyl 5-(3-aminopyridin-4-yl)-7-methyl-2-oxohexahydrooxazolo[4,5-c]pyridine-3(2H)-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CN(c2ccncc2N)C[C@@H]2[C@@H]1OC(=O)N2C(=O)OC(C)(C)C
Reaction #2007416
(3aR,7S,7aR)-tert-butyl 5-(3-aminopyridin-4-yl)-7-methyl-2-oxohexahydrooxazolo[4,5-c]pyridine-3(2H)-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(c2ccncc2N)C[C@@H]2[C@H]1OC(=O)N2C(=O)OC(C)(C)C
Reaction #2134013
(3aR,7R,7aS)-tert-butyl 5-(3-aminopyridin-4-yl)-7-methyl-2-oxohexahydrooxazolo[4,5-c]pyridine-3(2H)-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CN(c2ccncc2N)C[C@@H]2[C@@H]1OC(=O)N2C(=O)OC(C)(C)C
Reaction #2134015
(3aR,7S,7aR)-tert-butyl 5-(3-aminopyridin-4-yl)-7-methyl-2-oxohexahydrooxazolo[4,5-c]pyridine-3(2H)-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(c2ccncc2N)C[C@@H]2[C@H]1OC(=O)N2C(=O)OC(C)(C)C
Reaction #2279785
(3aR,7R,7aS)-tert-butyl 5-(3-aminopyridin-4-yl)-7-methyl-2-oxohexahydrooxazolo[4,5-c]pyridine-3(2H)-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CN(c2ccncc2N)C[C@@H]2[C@@H]1OC(=O)N2C(=O)OC(C)(C)C
Reaction #2279787
(3aR,7S,7aR)-tert-butyl 5-(3-aminopyridin-4-yl)-7-methyl-2-oxohexahydrooxazolo[4,5-c]pyridine-3(2H)-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1