Molecular Formula: C10H9BO2
Molecular weight: 171.98826
InChi: InChI=1S/C10H9BO2/c12-11(13)10-6-5-8-3-1-2-4-9(8)7-10/h1-7,12-13H
InChi Key: KPTRDYONBVUWPD-UHFFFAOYSA-N
SMILES: c12c(ccc(c1)B(O)O)cccc2
Chemical Name
(naphth-2-yl)boronic acid
2-naphthaleneboronic acid
2-Naphthyl-phenylboronic acid
naphthalene-2-boronic acid
β-naphthaleneboronic acids
β-naphthylboronic acid
(naphth-2-yl)boronic acid
2-naphthaleneboronic acid
2-Naphthyl-phenylboronic acid
naphthalene-2-boronic acid
β-naphthaleneboronic acids
β-naphthylboronic acid
Authors of compound
Naus, Petr
Holy, Antonin
Cibulka, Radek
Kotoucova, Hana
Dvorakova, Hana
Menova, Petra
Strnadova, Iveta
Kovandova, Martina
Chudoba, Josef
Hocek, Michal
Votruba, Ivan
Masojidkova, Milena
Pohl, Radek
Klepetarova, Blanka
Urban, Milan
Joubert, Nicolas
Otmar, Miroslav
Bambuch, Vitezslav
Slavetinska, Lenka
Dzubak, Petr
Hajduch, Marian
Birkus, Gabriel
Wang, Ting
Ray, Adrian S.
Cihlar, Tomas
Raindlova, Veronika
Pichova, Iva
Perlikova, Pavla
Bourderioux, Aurelie
Konecny, Petr
Stray, Kirsten M.
Feng, Joy Y.
Bahador, Gina
Eberlin, Ludovic
Tloustova, Eva
Lee, Yu-Jen
Holy, Antonin
Cibulka, Radek
Kotoucova, Hana
Dvorakova, Hana
Menova, Petra
Strnadova, Iveta
Kovandova, Martina
Chudoba, Josef
Hocek, Michal
Votruba, Ivan
Masojidkova, Milena
Pohl, Radek
Klepetarova, Blanka
Urban, Milan
Joubert, Nicolas
Otmar, Miroslav
Bambuch, Vitezslav
Slavetinska, Lenka
Dzubak, Petr
Hajduch, Marian
Birkus, Gabriel
Wang, Ting
Ray, Adrian S.
Cihlar, Tomas
Raindlova, Veronika
Pichova, Iva
Perlikova, Pavla
Bourderioux, Aurelie
Konecny, Petr
Stray, Kirsten M.
Feng, Joy Y.
Bahador, Gina
Eberlin, Ludovic
Tloustova, Eva
Lee, Yu-Jen
Articles
Cibulka, Radek;
Kotoucova, Hana;
Dvorakova, Hana;
Strnadova, Iveta;
Kovandova, Martina;
Chudoba, Josef, Biomimetic aerobic oxidative hydroxylation of arylboronic acids to phenols catalysed by a flavin derivative. Organic and Biomolecular Chemistry 2014, 12(13), 2137 - 2142, 10.1039/c3ob42081g 
.
.
Holy, Antonin;
Dvorakova, Hana;
Hocek, Michal;
Votruba, Ivan, Cytostatic 6-arylpurine nucleosides III. Synthesis and structure-activity relationship study in cytostatic activity of 6-aryl-, 6-hetaryl-and 6-benzylpurine ribonucleosides. Collect. Czech. Chem. Commun. 2001, 66(3), 483 - 499, 10.1135/cccc20010483 .
.
Hocek, Michal;
Pohl, Radek;
Klepetarova, Blanka, A new modular and practical methodology for the synthesis of 4- or 3-substituted phenyl C-nucleosides. European Journal of Organic Chemistry 2005(21), 4525 - 4528, 10.1002/ejoc.200500607 .
.
Hocek, Michal;
Pohl, Radek;
Urban, Milan;
Joubert, Nicolas, Modular Synthesis of 4-aryl- and 4-amino-substituted benzene C-2′-Deoxyribonucleosides. Synthesis 2008(12), 1918 - 1932, 10.1055/s-2008-1067038 .
.
Naus, Petr;
Hocek, Michal;
Votruba, Ivan;
Pohl, Radek;
Dzubak, Petr;
Hajduch, Marian;
Birkus, Gabriel;
Wang, Ting;
Ray, Adrian S.;
Cihlar, Tomas;
Pichova, Iva;
Perlikova, Pavla;
Bourderioux, Aurelie;
Konecny, Petr;
Stray, Kirsten M.;
Feng, Joy Y., Synthesis and significant cytostatic activity of 7-hetaryl-7- deazaadenosines. Journal of Medicinal Chemistry 2011, 54(15), 5498 - 5507, 10.1021/jm2005173 .
.
Naus, Petr;
Hocek, Michal;
Votruba, Ivan;
Pohl, Radek;
Slavetinska, Lenka;
Birkus, Gabriel;
Cihlar, Tomas;
Perlikova, Pavla;
Bourderioux, Aurelie;
Bahador, Gina, Sugar-modified derivatives of cytostatic 7-(het)aryl-7-deazaadenosines: 2′-C-methylribonucleosides, 2′-deoxy-2′- fluoroarabinonucleosides, arabinonucleosides and 2′-deoxyribonucleosides. Bioorganic and Medicinal Chemistry 2012, 20(17), 5202 - 5214, 10.1016/j.bmc.2012.07.003 .
.
Menova, Petra;
Hocek, Michal;
Slavetinska, Lenka;
Raindlova, Veronika;
Perlikova, Pavla;
Bahador, Gina;
Eberlin, Ludovic;
Tloustova, Eva;
Lee, Yu-Jen, Synthesis and Cytostatic and Antiviral Activities of 2′-Deoxy-2′,2′-difluororibo- and 2′-Deoxy-2′-fluororibonucleosides Derived from 7-(Het)aryl-7-deazaadenines. ChemMedChem 2013, 8(5), 832 - 846, 10.1002/cmdc.201300047 .
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