部分構造検索

NC(N)=O.OO

CCCN(CCC)C(=O)c1cc(C(N)=O)cc(C(=O)O)c1
Reaction #42275
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(OC(C)=O)c(OC)c2c1CCN(Cc1ccc(F)c(Cl)c1)C2=O
Reaction #46287
Ethyl 3-(acetyloxy)-6-(3-chloro-4-fluorobenzyl)-4-methoxy-5-oxo-5,6,7,8-tetrahydro-2,6-naphthyridine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(Nc3c(Cl)cncc3Cl)c(O)c(=O)oc2c1OC1CCCC1
Reaction #48910
8-(cyclopentyloxy)-4-(3,5-dichloropyridin-4-ylamino)-3-hydroxy-7-methoxy-2H-chromen-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CCCCC[C@H]1CC[C@H]([N+](C)([O-])S(=O)(=O)c2ccc(C(F)(F)F)cc2)CC1)CCO[Si](C)(C)C(C)(C)C
Reaction #53897
trans-N-[4-(5-{[2-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-ethyl-amino}-pentyl)-cyclohexyl]-N-methyl-4-trifluoromethyl-benzenesulfonamide N-oxide
収率 30.7%DOI: 10.6084/m9.figshare.5104873.v1
O[C@H]1C[C@H]2C[C@@H]1C[C@@H]2O
Reaction #74379
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc[n+]([O-])c1-c1cccc(C(=O)OC(C)(C)C)c1
Reaction #85463
2-(3-(tert-butoxycarbonyl)phenyl)-3-methylpyridine-1-oxide
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CCOCn1c2c[n+]([O-])c(Br)cc2c2ccc[n+]([O-])c21
Reaction #88593
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(C(F)(C(F)(F)F)C(F)(F)C(F)(F)F)cc(C)c1NC(=O)c1ccc2c(ccc(C#N)[n+]2[O-])c1
Reaction #157995
2-cyano-N-[2-ethyl-6-methyl-4-(1,1,1,2,3,3,4,4,4-nonafluorobutan-2-yl)phenyl]quinoline-6-carboxamide-1-oxide
収率 81.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1oc2cc(Br)ccc2c2ccc(Br)cc12
Reaction #159085
3,8-Dibromo-benzo[c]chromen-6-one
収率 134.5%DOI: 10.6084/m9.figshare.5104873.v1
O=c1oc2cc(Br)ccc2c2ccc(Br)cc12
Reaction #167031
3,8-Dibromo-benzo[c]chromen-6-one
収率 134.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)c[n+]([O-])c(C)c1Cl
Reaction #168876
title compound
収率 91.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc[n+]([O-])c1-c1cccc(C(=O)OC(C)(C)C)c1
Reaction #169522
2-(3-(tert-butoxycarbonyl)phenyl)-3-methylpyridine-1-oxide
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c2cc(Cc3cc[n+]([O-])c(Cl)c3)c3ccccc3c2ncn1[C@H]1CCOC[C@@H]1O
Reaction #169641
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCn1c(=O)n(-c2ccc(O[Si](C(C)C)(C(C)C)C(C)C)cc2)c2c1c(C)cc[n+]2[O-]
Reaction #169872
1-ethyl-7-methyl-3-(4-{[tris(1-methylethyl)silyl]oxy}phenyl)-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one 4-oxide
DOI: 10.6084/m9.figshare.5104873.v1
CCn1c(=O)n(-c2ccc(O[Si](C(C)C)(C(C)C)C(C)C)cc2)c2c1c(C)cc[n+]2[O-]
Reaction #169880
title compound
収率 19.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC1(CN(OC(=O)C(=O)OOC(C)(C)C)C(=O)OC(C)(C)C)NC(=O)N(CC(=O)c2ccccc2)C1=O
Reaction #265758
DOI: 10.1039/C8SC04228D
C=CC(=O)OOC(C)(CC)NC(=O)NCC
Reaction #281347
DOI: 10.1039/C8SC04228D
CCCCCCCCNC(=O)NC(=O)CCC(=O)OO
Reaction #290193
DOI: 10.1039/C8SC04228D
Cc1ccc[n+]([O-])c1-c1cccc(C(=O)OC(C)(C)C)c1
Reaction #329316
2-(3-(tert-butoxycarbonyl)phenyl)-3-methylpyridine-1-oxide
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)NC(=O)CCCC(=O)OO
Reaction #394080
DOI: 10.1039/C8SC04228D
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