shingo-sato documents

Xcode 6の新機能
Technology Xcode 6の新機能
日暮里アジャイル
Business 日暮里アジャイル
アプリエンジニアのデザインに対するこころがまえの話
Technology アプリエンジニアのデザインに対するこころがまえの話
俺のManaged Objectの使い方は間違っていた
Technology 俺のManaged Objectの使い方は間違っていた
Objective-Cで学ぶ英文法 (2)
Education Objective-Cで学ぶ英文法 (2)
re:日暮里アジャイル
Business re:日暮里アジャイル
ChemInform Abstract: Convenient Synthesis of 1,6,7,8-Substituted 2-(3′,4′-Substituted-phenyl)-4-quinolones via a 4-Ethoxyflavylium Salt
Documents ChemInform Abstract: Convenient Synthesis of 1,6,7,8-Substituted 2-(3′,4′-Substituted-phenyl)-4-quinolones via a 4-Ethoxyflavylium Salt
ChemInform Abstract: Direct Conversion to 2-Phenyl-4-quinolones via a 4-Alkoxyflavylium Salt from a Naturally Occurring Flavanone
Documents ChemInform Abstract: Direct Conversion to 2-Phenyl-4-quinolones via a 4-Alkoxyflavylium Salt from a Naturally Occurring Flavanone
ChemInform Abstract: Novel Glycosylation of the Nitroxyl Radicals with Peracetylated Glycosyl Fluorides Using a Combination of BF3×OEt2 and an Amine Base as Promoters
Documents ChemInform Abstract: Novel Glycosylation of the Nitroxyl Radicals with Peracetylated Glycosyl Fluorides Using a Combination of BF3×OEt2 and an Amine Base as Promoters
ChemInform Abstract: Synthesis of Carthamin Acetate, the Red Pigment in Safflower Petals
Documents ChemInform Abstract: Synthesis of Carthamin Acetate, the Red Pigment in Safflower Petals
Direct conversion to 2-phenyl-4-quinolones via a 4-alkoxyflavylium salt from a naturally occurring flavanone
Documents Direct conversion to 2-phenyl-4-quinolones via a 4-alkoxyflavylium salt from a naturally occurring flavanone
Synthesis of vicenin-1 and 3, 6,8- and 8,6-di-C-β-d-(glucopyranosyl-xylopyranosyl)-4′,5,7-trihydroxyflavones using two direct C-glycosylations of naringenin and phloroacetophenone
Documents Synthesis of vicenin-1 and 3, 6,8- and 8,6-di-C-β-d-(glucopyranosyl-xylopyranosyl)-4′,5,7-trihydroxyflavones using two direct C-glycosylations of naringenin and phloroacetophenone
Conversion of diacetyl-C-(β-d-glucopyranosyl)phloroglucinol to spiroketal compounds
Documents Conversion of diacetyl-C-(β-d-glucopyranosyl)phloroglucinol to spiroketal compounds
Synthesis and enzyme-catalyzed hydrolysis of a radical-masked glycosylated spin-label reagent
Documents Synthesis and enzyme-catalyzed hydrolysis of a radical-masked glycosylated spin-label reagent
A mild and environmentally friendly scandium(III) trifluoromethanesulfonate-catalyzed synthesis of bis(3′-indolyl)alkanes and bis(3′-indolyl)-1-deoxyalditols
Documents A mild and environmentally friendly scandium(III) trifluoromethanesulfonate-catalyzed synthesis of bis(3′-indolyl)alkanes and bis(3′-indolyl)-1-deoxyalditols
Total synthesis of two isoflavone C-glycosides: genistein and orobol 8-C-β-d-glucopyranosides
Documents Total synthesis of two isoflavone C-glycosides: genistein and orobol 8-C-β-d-glucopyranosides
Direct C-glycosylation of indole with unprotected mono-, di-, and trisaccharides: a one-pot synthesis of 1-deoxy-1,1-bis(3-indolyl)alditols
Documents Direct C-glycosylation of indole with unprotected mono-, di-, and trisaccharides: a one-pot synthesis of 1-deoxy-1,1-bis(3-indolyl)alditols
Synthesis and properties of umbelliferone-nitroxide radical hybrid compounds as fluorescence and spin-label probes
Documents Synthesis and properties of umbelliferone-nitroxide radical hybrid compounds as fluorescence and spin-label probes
Synthesis and spectral properties of polymethine-cyanine dye–nitroxide radical hybrid compounds for use as fluorescence probes to monitor reducing species and radicals
Documents Synthesis and spectral properties of polymethine-cyanine dye–nitroxide radical hybrid compounds for use as fluorescence probes to monitor reducing species and radicals
Efficient synthesis of analogs of safflower yellow B, carthamin, and its precursor: two yellow and one red dimeric pigments in safflower petals
Documents Efficient synthesis of analogs of safflower yellow B, carthamin, and its precursor: two yellow and one red dimeric pigments in safflower petals
Novel glycosylation of the nitroxyl radicals with peracetylated glycosyl fluorides using a combination of BF3·OEt2 and an amine base as promoters
Documents Novel glycosylation of the nitroxyl radicals with peracetylated glycosyl fluorides using a combination of BF3·OEt2 and an amine base as promoters