3Q1446 緑/赤色光変換をするフィトクロム型光受容体の解析(光生物_視覚・光受容4,第49回年会講演予稿集)
スポンサーリンク
概要
- 論文の詳細を見る
- 2011-08-15
著者
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Inomata Katsuhiko
Kanazawa Univ. Kanazawa Jpn
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Lagarias Clark
U. C. Davis Dpt . Mol. Cel. Biol.
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Hirose Yuu
Tokyo Univ. Grad. Sch. Front. Sci.
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Rockwell Nathan
U. C. Davis, Dpt . Mol. Cel. Biol.
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Martin Shelley
U. C. Davis, Dpt . Mol. Cel. Biol.
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Narikawa Rei
Tokyo Univ. Grad. Sch. Art. Sci.
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Ikeuchi Masahiko
Tokyo Univ. Grad. Sch. Art. Sci.
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Rockwell Nathan
U. C. Davis Dpt . Mol. Cel. Biol.
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Martin Shelley
U. C. Davis Dpt . Mol. Cel. Biol.
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Inomata Katsuhiko
Kanazawa Univ. Grad. Sch. Sci.
関連論文
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- "Syn-Effect" in the Conversion of (E)-α, β-Unsaturated Esters to the Corresponding β, γ-Unsaturated Esters
- "Syn-Effect"in the Isomerization of (E)-α-Fluorovinylic Sulfones to the Corresponding Allylic Sulfones under Basic Conditions
- STRUCTURAL FEATURES OF BILIN CHROMOPHORES NECESSARY FOR PHYTOCHROME-B MEDIATED REGULATION OF HYPOCOTYL GROWTH IN ARABIDOPSIS
- STRUCTURAL REQUIREMENT OF TETRAPYRROLE A∿D RINGS FOR ASSEMBLY WITH PHYTOCHROME-B AND PHOTOREVERSIBLE ABSORPTION CHANGE
- EFFECTS OF CHEMICALLY MODIFIED PHYCOCYANOBILIN ON LIGATION TO APOPHYTOCHROME-B AND PHOTOREVERSIBLE SPECTRAL CHANGE OF HOLO-PHYTOCHROME-B
- Asymmetric Addition of Alkynylzinc Reagents to Nitrones Utilizing Tartaric Acid Ester as a Chiral Auxiliary
- Total Syntheses of Doubly Locked Biliverdin Derivatives toward Elucidation of the Stereochemistry of Phytochrome Chromophore
- Syntheses of Biliverdin Derivatives Sterically Locked at the CD-Ring Components
- Synthesis of Biliverdin Derivative Bearing the Sterically Fixed E-anti C/D-Ring Component
- Synthesis of the Sterically Fixed Biliverdin Derivative Bearing the Z-anti C/D-Ring Component
- An Efficient Method for the Conversion of 2-Bromo-5-tosylpyrroles to the Corresponding 5-Tosylpyrrolinones as the D-Ring of Phycocyanobilin Derivatives
- Total Syntheses of Phycocyanobilin Derivatives Bearing a Modified A-Ring toward the Structure/Function Analysis of Phytochrome
- Efficient Synthesis of B- and C-Rings Components of Phycobilin Derivatives for Structure/Function Analysis of Phytochrome
- An Efficient Method to Construct the A,B-Rings Component toward Total Syntheses of Phycocyanobilin and Its Derivative as a Photoprobe
- Total Syntheses of (±)-Phycocyanobilin and Its Derivatives Bearing a Photoreactive Group at D-ring
- Syntheses of 3,4-Disubstituted 2-Tosylpyrroles and 5-Tosyl-1,5-dihydro-2H-pyrrol-2-ones Starting from Ethyl 3,4-Disubstituted 2-Pyrrolecarboxylates
- Convenient and Regioselective Syntheses of 3, 4-Disubsutituted Δ^3-Pyrrolin-2-one Derivatives Starting from 2-Tosyl-3, 4-Disubstituted Pyrroles
- Asymmetric 1,3-Dipolar Cycloaddition of Nitrones with an Electron-Withdrawing Group to Allylic Alcohols Utilizing Diisopropyl Tartrate as a Chiral Auxiliary
- Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Imines to Homoallytic Alcohols
- Asymmetric 1,3-Dipolar Cycloaddition Reaction of Azomethine Imines to Allyl Alcohol
- Catalytic Asymmetric Addition of Alkynylzinc Reagents to Nitrones
- The First Enantioselective Hetero Diels-Alder Reaction of Nitroso Compound Utilizing Tartaric Acid Ester as a Chiral Auxiliary
- Catalytic Asymmetric 1,3-Dipolar Cycloaddition of a Nitrone Bearing a Bulky Amide Moiety to γ-Substituted Allylic Alcohols
- A Catalytic Asymmetric 1,3-Dipolar Cycloaddition of Nitrones to Allyl Alcohol
- Total Syntheses of Sterically Locked Phycocyanobilin Derivatives Bearing a 15Z-anti or a 15E-anti CD-Ring Component
- 3Q1446 緑/赤色光変換をするフィトクロム型光受容体の解析(光生物_視覚・光受容4,第49回年会講演予稿集)