Noyori, Ryōji 1938-....
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
- 200 _ | ‡a Noyori ‡b Ryōji ‡f 1938-....
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- 100 1 _ ‡a Noyori, Ryoji ‡d 1938-
- 100 1 _ ‡a Noyori, Ryoji ‡d 1938-...
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- 100 1 _ ‡a Noyori, Ryoji, ‡d 1938-
- 100 1 _ ‡a Noyori, Ryoji, ‡d 1938-....
- 100 1 _ ‡a Noyori, Ryōji
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- 100 0 _ ‡a 野依 良治
- 100 1 _ ‡a 野依, 良治
- 100 1 _ ‡a 野依, 良治, ‡d 1938-
4xx's: Alternate Name Forms (75)
Works
Title | Sources |
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Ab initio molecular orbitals study of the conformational preference in alpha-cyano-alpha-fluorophenylacetic acid ester | |
Asymmetric catalysis in organic synthesis | |
Asymmetric catalysis: science and opportunities (Nobel lecture). | |
Asymmetric hydrogenation of .beta.-keto carboxylic esters. A practical, purely chemical access to .beta.-hydroxy esters in high enantiomeric purity | |
Benzimidazolium Triflate as an Efficient Promoter for Nucleotide Synthesis via the Phosphoramidite Method | |
The Chemical Society of Japan : a 125-year quest for exellence : 1878-2003 | |
Chiral eta | |
Chiral eta(6)-arene/N-tosylethylenediamine-ruthenium(II) complexes: solution behavior and catalytic activity for asymmetric hydrogenation | |
Compounds with two carbon-heteroatom bonds : acetals : O/N, S/S, S/N and N/N and higher heteroatom analogues | |
Conformationally Flexible Biphenyl-phosphane Ligands for Ru-Catalyzed Enantioselective Hydrogenation | |
Converging and Integrating Our Knowledge to Sustain Humanity | |
Direct C-H arylation of (hetero)arenes with aryl iodides via rhodium catalysis | |
Enantioselective Addition of Organometallic Reagents to Carbonyl Compounds: Chirality Transfer, Multiplication, and Amplification | |
Facts are the enemy of truth-reflections on serendipitous discovery and unforeseen developments in asymmetric catalysis | |
Gakkō o inobēshon-suru 14 no kyōikuron | |
Gakumon to sōzō : Nōberushō kagakusha noyori ryōji hakushi | |
Gendai yuki kagaku. | |
Green oxidation with aqueous hydrogen peroxide | |
Homogeneous catalytic hydrogenation of supercritical carbon dioxide | |
Hydration of terminal alkynes catalyzed by water-soluble cobalt porphyrin complexes | |
The hydrogenation/transfer hydrogenation network in asymmetric reduction of ketones catalyzed by [RuCl2 | |
Jijitsu wa shinjitsu no teki nari : Watakushi no rirekisho | |
Jinsei wa ito o koete : Noberu kagakusho eno michi. | |
Kagaku shizen to shakai eno kakawari : Dai 17kai daigaku to kagaku kokai shinpojiumu koen shurokushu. | |
Kenkyū wa mizumizushiku : Nōberu kagakushō no kotoba | |
Kinetic Resolution of Racemic Secondary Alcohols by RuII-Catalyzed Hydrogen Transfer | |
Mechanism of asymmetric hydrogenation of alpha-(acylamino)acrylic esters catalyzed by BINAP-ruthenium(II) diacetate | |
Molecules that changed the world : a brief history of the art and science of synthesis and its impact on society | |
Molecules that changed the world / K. C. Nicolaou, T. Montagnon. - Weinheim, cop. 2008. | |
The Nagoya COE Conference on Molecular Mechanism of Biofunctions, Oct. 30 and 31, 1997 | |
One-pot nitrile aldolization/hydration operation giving β-hydroxy carboxamides | |
Organic chemistry. | |
Organometallics : compounds of groups 13 and 2 (Al, Ga, In, Tl, Be-Ba) | |
Practical synthesis of optically active styrene oxides via reductive transformation of 2-chloroacetophenones with chiral rhodium catalysts | |
Pursuing practical elegance in chemical synthesis | |
Rh-catalyzed arylation and alkenylation of C(60) using organoboron compounds | |
Salt | |
Solution structures and behavior of trans-RuH(eta(1)-BH(4)) (binap)(1,2-diamine) complexes. | |
Sulfonyl-Stabilized Oxiranyllithium-Based Approach to Polycyclic Ethers. Convergent Synthesis of the ABCDEF-Ring System of Yessotoxin and Adriatoxin | |
Supercritical Fluids: Introduction | |
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 | |
Synthesis of novel pyrimidine C-nucleosides | |
Synthesis of the ABCD ring of gambierol | |
Synthesizing our future | |
Toward efficient asymmetric hydrogenation: architectural and functional engineering of chiral molecular catalysts | |
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 | |
trans-RuH(eta1-BH4)(binap)(1,2-diamine): a catalyst for asymmetric hydrogenation of simple ketones under base-free conditions | |
Vibrant Science Needed for Future Society | |
Why p-Cymene? Conformational effect in asymmetric hydrogenation of aromatic ketones with a η(6) -arene/ruthenium(II) catalyst | |
ウォーレン有機化学. | |
グリーン化学に向けた高機能性触媒の開拓 | |
スーパーアニオン種の合成と反応 | |
不斉合成 : 右手形と左手形分子のつくり分け | |
事実は真実の敵なり : 私の履歴書 | |
人生は意図を超えて : ノーベル化学賞への道 | |
分子構造と反応・有機金属化学 | |
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 | |
大学院講義有機化学. | |
学問と創造 : ノーベル賞化学者野依良治博士 | |
学術研究の実態に関する調査研究 | |
学校をイノベーションする14の教育論 | |
研究はみずみずしく : ノーベル化学賞の言葉 | |
新有機化学反応の開拓と生理活性物質の化学合成 | |
有機亜鉛化合物の触媒的不斉反応の機構 | |
有機合成化学・生物有機化学 | |
現代有機化学. | |
高選択的不斉水素化反応の開拓 |