<Abstract of published report>Tetracyanoethylene-Hydrogen Peroxide, a Mild Epoxidation System of Olefins.
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- Oxidative Photo-Decarboxylation in the Presence of Mesoporous Silicas
- Oxidative Transformation of Arylmethyl Bromides and Alcohols with a Combination of Mesoporous Silica FSM-16 and Alkali Iodides under Photoirradiation.
- Photooxidation of Arylmethyl Bromides with Mesoporous Silica FSM-16.
- New Synthetic Method of Imides through Oxidative Photodecarboxylation Reaction of N-Protected α-Amino Acids with FSM-16.
- Oxidative Photodecarboxylation of α-Hydroxycarboxylic Acids and Phenylacetic Acid Derivatives with FSM-16.
- New Synthetic Method of Imides through Oxidative Photodecarboxylation Reaction of N-Protected α-Amino Acids with FSM-16
- Synthesis of (R)-(+)-Tanikolide through Stereospecific C-H Insertion Reaction of Dichlorocarbene with Optically Active Secondary Alcohol Derivatives
- Stereospecific Construction of Chiral Quaternary Carbon Compounds from Chiral Secondary Alcohol Derivatives
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- Polymer-Supported Dicyanoketene Acetal as a π-Acid Catalyst : Monothioacetalization and Carbon-Carbon Bond Formation of Acetals.
- Polymer-Supported Dicyanoketene Acetal as a π-Acid Catalyst : Monothioacetalization and Carbon-Carbon Bond Formation of Acetals
- Unprecedented Polymer-supported π-Acid : Synthesis and Its Application as a Promoter to the Monothioacetalization of Acetals.
- Mild Esterification and Transesterification of Carboxylic Acids Catalyzed by Tetracyanoethylene and Dicyanoketene Dimethyl Acetal
- Mild Esterification and Transesterification of Carboxylic Acids Catalyzed by Tetracyanoethylene and Dicyanoketene Dimetheyl Acetal
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- Regio-and Stereoselective Terminal Allylic Carboxymethylation of gem-Dimethyl Olefins. Synthesis of Biologically Important Linear Degraded Terpenoids
- Synthetic Studies on Isoprenoidquinones. I. A Facile Regioand Stereocontrolled Synthesis of Protected Hydroquinones with an Omega-Hydroxyprenyl or Omega-Hydroxygeranyl Side Chain
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- Synthetic Studies on Isoprenoidquinones. II. Syntheses of Ubiquinone-10,Phylloquinone, and Menaquinone-4 by a Chain-Extending Method Utilizing Terminally Functionalized Isoprenoidhydroquinones
- HIGHLY STEREOSELECTIVE SYNTHESIS AND STRUCTURAL CONFIRMATION OF A FUNGAL METABOLITE, LL-P880β
- Preparation of Nitroalkenes : Substitution Reaction via Addition-Elimination Using β-Nitrovinyl Sulfoxides.
- Hard Acid and Soft Nucleophile Systems. Part 12. : Regioselective Functionalization of 1,3-Dienes through the Lewis Acid Mediated Thienium Cation Diels-Alder Reaction.
- Facile Synthesis of Optically Active Tertiary Alcohol Building Blocks by Stereospecific C-H Insertion Reaction of Dichlorocarbene with Secondary Alcohol Derivatives.
- Facile Synthesis of Optically Active Tertiary Alcohol Building Blocks by Stereospecific C - H Insertion Reaction of Dichlorocarbene with Secondary Alcohol Derivatives
- Total Synthesis of (+)-Asperlin Starting with (S, S)-Tartaric Acid.
- Total Synthesis of (+)-Asperlin Starting with (S,S)-Tartaric Acid
- Catalytic Activity of Isoborneol-Derived Sulfides in Asymmetric Addition of Diethylzinc to Benzaldehyde
- Addition-Elimination Strategy for Asymmetric Induction : A Chiral Sulfoxide as a Leaving Group.
- Deprotection of a Silyl Group with Mesoporous Silica
- New Synthetic Method of Benzaldehydes and α, β-Unsaturated Aldehydes with I_2under Photoirradiation.
- New Synthetic Method of Benzaldehydes and α,β-Unsaturated Aldehydes with I_2 under Photoirradiation
- Selective Deprotection of Triethylsilyl Group in the Presence of t-Butyldimethylsilyl Group with MCM-41/MeOH Heterogeneous System.
- Selective Acceleration for Deprotection of Benzyl Ethers with Ti-HMS
- Short-Step Synthesis of Chiral C_2-Symmetric 2,3,4,5-Tetrasubstituted Pyrrolidines from D-Mannitol and Their Use as Chiral Ligands in the Reaction of Diethylzinc and Benzaldehyde.
- Studies on Indolizines and Azaindolizines. I. The 1,3-Dipolar Cycloaddition of Acetylenic Compounds to Pyridazinium Ylides
- Synthesis and Investigation of C_2-Symmetric Optically Active Pyrrolidinium Salts as Chiral Phase-Transfer Catalysts
- Alcoholysis of Epoxides Catalyzed by Tetracyanoethylene and Dicyanoketene Acetals.
- Alocoholysis of Epoxides Catalyzed by Tetracyanoethylene and Dicyanoketene Acetals
- Alcoholysis of Epoxides Catalyzed by Tetracyanoethylene
- Substrate-Specific Rearrangement and Acetonidation of Epoxy-Ethers Catalyzed by Tetracyanoethylen
- Substrate-Specific Rearrangement and Acetonidation of Epoxy-Ethers Catalyzed by Tetracyanoethylene
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- Synthesis and Structure of 1-(Diacetoxyiodo)-2,4,6-tri-tert-butylbenzen and Its Analogues.
- Inversion of Configuration in Nucleophilic Vinylic Substitutions of (E)-β-Alkylvinyliodonium Tetrafluoroborates with Halides.
- Generation of Allenyliodinanes and Their Reductive Indonio-Claisen Rearrangement.
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- Synthesis of (3S,4S)-Statine and a Related Compound, (3S,4S)-AHPPA, from _D-Glucosamine as a Chiral Pool
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