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10887

O=C1c2ccccc2C(=O)N1c1ncnc2c1ncn2OCc1ccccc1
Reaction #6347
title compound
Выход 49.0%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc(N2C(=O)c3ccccc3C2=O)cc1
Reaction #66415
titled compound
Выход 90.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1cnc(N2C(=O)c3ccccc3C2=O)nc1
Reaction #66423
(tert-butoxy)-N-[2-(1,3-dioxobenzo[c]azolidin-2-yl)pyrimidin-5-yl]carboxamide
Выход 91.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(=O)c2cc(Cl)ccc21
Reaction #246949
DOI: 10.1039/C8SC04228D
O=C1c2ccccc2C(=O)N1c1nc2ccccc2[nH]1
Reaction #290448
DOI: 10.1039/C8SC04228D
NC(=O)c1ccc(C(=O)O)c(C(N)=O)c1
Reaction #411519
2,4-dicarbamoylbenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1ccc(C(N)=O)c(C(=O)O)c1
Reaction #411521
2,5-dicarbamoylbenzoic acid
Выход 89.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1c1ncnc2c1ncn2OCc1ccccc1
Reaction #461077
title compound
Выход 49.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Br)c(CCN2C(=O)c3ccccc3C2=O)cc1OC
Reaction #475378
crude product
DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc(N2C(=O)c3ccccc3C2=O)cc1
Reaction #649848
titled compound
Выход 90.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1cnc(N2C(=O)c3ccccc3C2=O)nc1
Reaction #649856
(tert-butoxy)-N-[2-(1,3-dioxobenzo[c]azolidin-2-yl)pyrimidin-5-yl]carboxamide
Выход 91.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(C)(C)C)c(OC(=O)c2ccccc2C(=O)Oc2c(C(C)(C)C)cc(C)cc2C(C)(C)C)c(C(C)(C)C)c1
Reaction #655511
Compound 6
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1c1nc2ccccc2[nH]1
Reaction #683755
N-(benzimidazol-2-yl)phthalimide
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Br)c(CCN2C(=O)c3ccccc3C2=O)cc1OC
Reaction #710579
crude product
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)c2ccccc21
Reaction #736455
9,10-anthraquinone
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)c2c(O)ccc(O)c21
Reaction #736456
1,4-dihydroxy-9,10-anthraquinone
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(O)c2c(c1O)C(=O)c1ccccc1C2=O
Reaction #736457
2-methyl-1,4-dihydroxy-9,10-anthraquinone
Выход 62.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccc([N+](=O)[O-])cc2C(=O)c2c(O)ccc(O)c21
Reaction #736458
6-nitro-1,4-dihydroxy-9,10-anthraquinone
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)c2c1ccc(O)c2O
Reaction #736459
1,2-dihydroxy-9,10-anthraquinone
Выход 55.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)c2c(O)c3c(c(O)c21)CCCC3
Reaction #736460
6,11-dihydroxy-7,8,9,10-tetrahydro-5,12-naphtacenequinone
Выход 88.0%DOI: 10.6084/m9.figshare.5104873.v1
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