Noyori, Ryōji 1938-....
![Sudoc [ABES], France](/viaf/images/flags/SUDOC.png "Sudoc [ABES], France")
野依, 良治
Noyori, Ryōji
野依, 良治, 1938-
נויורי, ריוג'י
VIAF ID: 85075841 (Personal)
Permalink: http://viaf.org/viaf/85075841
Preferred Forms
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200 _ |
‡a
Noyori
‡b
Ryōji
‡f
1938-....
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100 1 _ ‡a Noyori, Ryoji
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100 1 _ ‡a Noyori, Ryoji
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100 1 _ ‡a Noyori, Ryoji
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100 1 _ ‡a Noyori, Ryoji
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100 1 _ ‡a Noyori, Ryoji
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100 1 _ ‡a Noyori, Ryoji ‡d (1938- ).
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100 1 _
‡a
Noyori, Ryoji
‡d
1938-
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100 1 _
‡a
Noyori, Ryoji
‡d
1938-...
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100 1 _
‡a
Noyori, Ryoji,
‡d
1938-
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100 1 _ ‡a Noyori, Ryoji, ‡d 1938-
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100 1 _
‡a
Noyori, Ryoji,
‡d
1938-....
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100 1 _
‡a
Noyori, Ryōji
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100 1 _ ‡a נויורי, ריוג'י
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100 0 _
‡a
野依 良治
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100 1 _
‡a
野依, 良治
-
100 1 _
‡a
野依, 良治,
‡d
1938-
4xx's: Alternate Name Forms (76)
Works
| Title | Sources |
|---|---|
| Ab initio molecular orbitals study of the conformational preference in alpha-cyano-alpha-fluorophenylacetic acid ester |
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| Asymmetric catalysis in organic synthesis |
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| Asymmetric catalysis: science and opportunities (Nobel lecture). |
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| Asymmetric hydrogenation of .beta.-keto carboxylic esters. A practical, purely chemical access to .beta.-hydroxy esters in high enantiomeric purity |
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| Benzimidazolium Triflate as an Efficient Promoter for Nucleotide Synthesis via the Phosphoramidite Method |
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| The Chemical Society of Japan : a 125-year quest for exellence : 1878-2003 |
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| Chiral eta |
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| Chiral eta(6)-arene/N-tosylethylenediamine-ruthenium(II) complexes: solution behavior and catalytic activity for asymmetric hydrogenation |
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| Compounds with two carbon-heteroatom bonds : acetals : O/N, S/S, S/N and N/N and higher heteroatom analogues |
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| Conformationally Flexible Biphenyl-phosphane Ligands for Ru-Catalyzed Enantioselective Hydrogenation |
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| Converging and Integrating Our Knowledge to Sustain Humanity |
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| Direct C-H arylation of (hetero)arenes with aryl iodides via rhodium catalysis |
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| Enantioselective Addition of Organometallic Reagents to Carbonyl Compounds: Chirality Transfer, Multiplication, and Amplification |
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| Facts are the enemy of truth-reflections on serendipitous discovery and unforeseen developments in asymmetric catalysis |
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| Gakkō o inobēshon-suru 14 no kyōikuron |
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| Gakumon to sōzō : Nōberushō kagakusha noyori ryōji hakushi |
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| Gendai yūki kagaku. |
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| Green oxidation with aqueous hydrogen peroxide |
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| Homogeneous catalytic hydrogenation of supercritical carbon dioxide |
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| Hydration of terminal alkynes catalyzed by water-soluble cobalt porphyrin complexes |
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| The hydrogenation/transfer hydrogenation network in asymmetric reduction of ketones catalyzed by [RuCl2 |
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| Jijitsu wa shinjitsu no teki nari : Watakushi no rirekisho |
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| Jinsei wa ito o koete : Noberu kagakusho eno michi. |
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| Kagaku shizen to shakai eno kakawari : Dai 17kai daigaku to kagaku kokai shinpojiumu koen shurokushu. |
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| Kenkyū wa mizumizushiku : Nōberu kagakushō no kotoba |
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| Kinetic Resolution of Racemic Secondary Alcohols by RuII-Catalyzed Hydrogen Transfer |
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| Mechanism of asymmetric hydrogenation of alpha-(acylamino)acrylic esters catalyzed by BINAP-ruthenium(II) diacetate |
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| Molecules that changed the world : a brief history of the art and science of synthesis and its impact on society |
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| Molecules that changed the world / K. C. Nicolaou, T. Montagnon. - Weinheim, cop. 2008. |
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| The Nagoya COE Conference on Molecular Mechanism of Biofunctions, Oct. 30 and 31, 1997 |
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| One-pot nitrile aldolization/hydration operation giving β-hydroxy carboxamides |
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| Organic chemistry. |
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| Organometallics : compounds of groups 13 and 2 (Al, Ga, In, Tl, Be-Ba) |
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| Practical synthesis of optically active styrene oxides via reductive transformation of 2-chloroacetophenones with chiral rhodium catalysts |
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| Pursuing practical elegance in chemical synthesis |
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| Rh-catalyzed arylation and alkenylation of C(60) using organoboron compounds |
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| Salt |
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| Solution structures and behavior of trans-RuH(eta(1)-BH(4)) (binap)(1,2-diamine) complexes. |
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| Sulfonyl-Stabilized Oxiranyllithium-Based Approach to Polycyclic Ethers. Convergent Synthesis of the ABCDEF-Ring System of Yessotoxin and Adriatoxin |
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| Supercritical Fluids: Introduction |
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| Synthesis of 11C-labelled N,N'-diphenylurea and ethyl phenylcarbamate by a rhodium-promoted carbonylation via [11C]isocyanatobenzene using phenyl azide and [11C]carbon monoxide |
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| Synthesis of novel pyrimidine C-nucleosides |
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| Synthesis of the ABCD ring of gambierol |
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| Synthesizing our future |
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| Toward efficient asymmetric hydrogenation: architectural and functional engineering of chiral molecular catalysts |
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| trans-[RuCl2 (phosphane)2 (1,2-diamine)] and Chiral trans-[RuCl2 (diphosphane)(1,2-diamine)]: Shelf-Stable Precatalysts for the Rapid, Productive, and Stereoselective Hydrogenation of Ketones |
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| trans-RuH(eta1-BH4)(binap)(1,2-diamine): a catalyst for asymmetric hydrogenation of simple ketones under base-free conditions |
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| Vibrant Science Needed for Future Society |
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| Why p-Cymene? Conformational effect in asymmetric hydrogenation of aromatic ketones with a η(6) -arene/ruthenium(II) catalyst |
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| ウォーレン有機化学. |
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| グリーン化学に向けた高機能性触媒の開拓 |
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| スーパーアニオン種の合成と反応 |
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| 不斉合成 : 右手形と左手形分子のつくり分け |
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| 事実は真実の敵なり : 私の履歴書 |
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| 人生は意図を超えて : ノーベル化学賞への道 |
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| 分子構造と反応・有機金属化学 |
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| 化学:自然と社会へのかかわり : 第17回「大学と科学」公開シンポジウム講演収錄集 |
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| 大学院講義有機化学. |
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| 学問と創造 : ノーベル賞化学者野依良治博士 |
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| 学術研究の実態に関する調査研究 |
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| 学校をイノベーションする14の教育論 |
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| 研究はみずみずしく : ノーベル化学賞の言葉 |
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| 新有機化学反応の開拓と生理活性物質の化学合成 |
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| 有機亜鉛化合物の触媒的不斉反応の機構 |
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| 有機合成化学・生物有機化学 |
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| 現代有機化学. |
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| 高選択的不斉水素化反応の開拓 |
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