Naoyuki Hanaki

ORCID: 0009-0007-4449-3192
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Research Areas
  • Chemical Synthesis and Reactions
  • Synthetic Organic Chemistry Methods
  • Asymmetric Synthesis and Catalysis
  • Asymmetric Hydrogenation and Catalysis
  • Advanced Synthetic Organic Chemistry
  • Chemical Synthesis and Analysis
  • Carbohydrate Chemistry and Synthesis
  • Phenothiazines and Benzothiazines Synthesis and Activities
  • Sulfur-Based Synthesis Techniques
  • Plant Reproductive Biology
  • Plant Molecular Biology Research
  • Chemical Synthesis and Characterization
  • Analytical Methods in Pharmaceuticals
  • Synthesis and Biological Activity
  • Synthesis and Biological Evaluation
  • Quinazolinone synthesis and applications
  • Polyoxometalates: Synthesis and Applications
  • Cyclopropane Reaction Mechanisms
  • Polysaccharides and Plant Cell Walls
  • Light effects on plants
  • Model-Driven Software Engineering Techniques
  • Organoboron and organosilicon chemistry
  • Carbon dioxide utilization in catalysis
  • Synthesis of heterocyclic compounds
  • Antibiotics Pharmacokinetics and Efficacy

Nagoya University
1991-2000

Irvine University
2000

University of California, Irvine
1999

Japan Science and Technology Agency
1998

In the higher plant, Arabidopsis thaliana, results from recent intensive studies suggested that His-to-Asp phosphorelay mechanisms are involved presumably in propagation of environmental stimuli, such as phytohormones (e.g. ethylene and cytokinin). Here we identified characterized a set novel genes whose products considerably resemble authentic response regulators (ARR-series) sense they have phospho-accepting receiver-like domain. However, should be discriminated classical ones strict lack...

10.1093/pcp/41.6.791 article EN Plant and Cell Physiology 2000-06-01

His-Asp phosphorelays are evolutionary-conserved powerful biological tactics for intracellular signal transduction. Such a phosphorelay is generally made up of "sensor histidine (His)-kinases", "response regulators", and "histidine-containing (HPt) phosphotransmitters". In the higher plant, Arabidopsis thaliana, results from recent intensive studies suggested that may be widely used propagating environmental stimuli, such as phytohormones (e.g., ethylene cytokinin). this study, we first...

10.1093/oxfordjournals.pcp.a029600 article EN Plant and Cell Physiology 1999-01-01

Abstract Tris(pentafluorophenyl)boron is an efficient, air stable, and water tolerant Lewis acid catalyst for the aldol-type Michael reactions of silyl enol ethers with carbonyl compounds or other electrophiles (trimethyl orthoformate, dimethyl acetal, chloromethyl methyl ether), allylation reaction allylsilanes aldehydes, Diels–Alder dienes α,β-unsaturated aldehydes. A solution formaldehyde in applicable as electrophile. Also, ketene acetals aromatic aliphatic imines successfully carried...

10.1246/bcsj.68.1721 article EN Bulletin of the Chemical Society of Japan 1995-06-01

ADVERTISEMENT RETURN TO ISSUEPREVCommunicationNEXTAntimony-Templated Macrolactamization of Tetraamino Esters. Facile Synthesis Macrocyclic Spermine Alkaloids, (±)-Buchnerine, (±)-Verbacine, (±)-Verbaskine, and (±)-VerbascenineKazuaki Ishihara, Yoshichika Kuroki, Naoyuki Hanaki, Suguru Ohara, Hisashi YamamotoView Author Information School Engineering, Nagoya University Furo-cho, Chikusa, 464-01, Japan Cite this: J. Am. Chem. Soc. 1996, 118, 6, 1569–1570Publication Date (Web):February 14,...

10.1021/ja953541a article EN Journal of the American Chemical Society 1996-01-01

The aldol-type reaction of ketene silyl acetals with aromatic or aliphatic imines is successfully carried out using tris(pentafluorophenyl)boron as a catalyst (0.2~10 mol%).

10.1055/s-1994-23065 article EN Synlett 1994-01-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTHighly diastereoselective acetal cleavages using novel reagents prepared from organoaluminum and pentafluorophenolKazuaki Ishihara, Naoyuki Hanaki, Hisashi YamamotoCite this: J. Am. Chem. Soc. 1993, 115, 23, 10695–10704Publication Date (Print):November 1, 1993Publication History Published online1 May 2002Published inissue 1 November 1993https://pubs.acs.org/doi/10.1021/ja00076a030https://doi.org/10.1021/ja00076a030research-articleACS...

10.1021/ja00076a030 article EN Journal of the American Chemical Society 1993-11-01

Tris(pentafluorophenyl)boron is an efficient Lewis acid catalyst for stereoselective rearrangement of epoxides to carbonyl compounds.

10.1055/s-1995-5049 article EN Synlett 1995-07-01

[reaction: see text] The condensation of allylic diols with unsymmetrical ketones proceeds high stereoselection to form 2,2-disubstituted 4-acyltetrahydrofurans when the alpha-substituents ketone differ substantially in size. A Prins-pinacol this type is central strategic step an enantioselective synthesis (-)-citreoviral.

10.1021/ol991315q article EN Organic Letters 1999-12-23

Abstract The total synthesis of spermidine and spermine alkaloids, (S)-(+)-dihydroperiphylline (1), (±)-buchnerine (2), (±)-verbacine (3), (±)-verbaskine (4), (±)-verbascenine (5), is described. construction macrocyclic lactams has been efficiently accomplished by the metal-templated cyclization triamino esters tetraamino esters. It was also found that antimony(III) ethoxide useful as an intermolecular amidation catalyst.

10.1246/bcsj.71.1221 article EN Bulletin of the Chemical Society of Japan 1998-05-01

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTHighly selective acetal cleavage using new organoaluminum reagentsKazuaki Ishihara, Naoyuki Hanaki, and Hisashi YamamotoCite this: J. Am. Chem. Soc. 1991, 113, 18, 7074–7075Publication Date (Print):August 1, 1991Publication History Published online1 May 2002Published inissue 1 August 1991https://pubs.acs.org/doi/10.1021/ja00018a075https://doi.org/10.1021/ja00018a075research-articleACS PublicationsRequest reuse permissionsArticle...

10.1021/ja00018a075 article EN Journal of the American Chemical Society 1991-08-01

The reaction of acetals derived from (-)-(2R,4R)-2,4-pentanediol and ketones in the presence a catalytic amount aluminum pentafluorophenoxide produces reductively cleaved products with high diastereoselectivity. is new method for diastereoselective cleavage acetals: an intramolecular Meerwein-Ponndorf-Verley reductive Oppenauer oxidative on acetal template.

10.1055/s-1993-22373 article EN Synlett 1993-01-01

Highly regio- and stereo-selective annulation–elimination reactions of 1-cycloalkenyl 3-hydroxypropyl ethers in the presence triflic anhydride tertiary amines are described; bicyclic vinyl produced converted to 2-substituted δ-lactones, macrocyclic oxolactones hydroxy by ozonolysis stereoselective hydroboration.

10.1039/c39950001117 article EN Journal of the Chemical Society Chemical Communications 1995-01-01

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at glance that was extracted from about 100 leading journals. To access of an article which published elsewhere, please select “Full Text” option. The original trackable via the “References”

10.1002/chin.199509085 article EN ChemInform 1995-02-28

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at glance that was extracted from about 100 leading journals. To access of an article which published elsewhere, please select “Full Text” option. The original trackable via the “References”

10.1002/chin.199547071 article EN ChemInform 1995-11-21

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at glance that was extracted from about 100 leading journals. To access of an article which published elsewhere, please select “Full Text” option. The original trackable via the “References”

10.1002/chin.200016259 article EN ChemInform 2000-04-18

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at glance that was extracted from about 100 leading journals. To access of an article which published elsewhere, please select “Full Text” option. The original trackable via the “References”

10.1002/chin.199834256 article EN ChemInform 1998-08-25

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at glance that was extracted from about 100 leading journals. To access of an article which published elsewhere, please select “Full Text” option. The original trackable via the “References”

10.1002/chin.199638147 article EN ChemInform 1996-09-17

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at glance that was extracted from about 100 leading journals. To access of an article which published elsewhere, please select “Full Text” option. The original trackable via the “References”

10.1002/chin.199624226 article EN ChemInform 1996-06-11

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at glance that was extracted from about 100 leading journals. To access of an article which published elsewhere, please select “Full Text” option. The original trackable via the “References”

10.1002/chin.199541188 article EN ChemInform 1995-10-10

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at glance that was extracted from about 100 leading journals. To access of an article which published elsewhere, please select “Full Text” option. The original trackable via the “References”

10.1002/chin.199542056 article EN ChemInform 1995-10-17

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at glance that was extracted from about 100 leading journals. To access of an article which published elsewhere, please select “Full Text” option. The original trackable via the “References”

10.1002/chin.199409054 article EN ChemInform 1994-03-01

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at glance that was extracted from about 100 leading journals. To access of an article which published elsewhere, please select “Full Text” option. The original trackable via the “References”

10.1002/chin.199416050 article EN ChemInform 1994-04-19

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at glance that was extracted from about 100 leading journals. To access of an article which published elsewhere, please select “Full Text” option. The original trackable via the “References”

10.1002/chin.199149076 article EN ChemInform 1991-12-10
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