H. Nakatsuji

发表

Practical and robust method for stereoselective preparations of ketene silyl (thio)acetal derivatives and NaOH-catalyzed crossed-Claisen condensation between ketene silyl acetals and methyl esters

A. Iida, K. Takai, Yuuya Nawate, 2009 .

Mild, powerful, and robust methods for esterification, amide formation, and thioesterification between acid chlorides and alcohols, amines, thiols, respectively

H. Nakatsuji, Y. Tanabe, M. Morimoto, 2007 .

A General and Robust Method for the Preparation of (E)- and (Z)-Stereodefined Fully Substituted Enol Tosylates: Promising Cross-Coupling Partners

H. Nakatsuji, Y. Tanabe, Yuka Sato, 2016 .

Water Solvent Method for Esterification and Amide Formation between Acid Chlorides and Alcohols Promoted by Combined Catalytic Amines: Synergy between N-Methylimidazole and N,N,N′,N′-Tetramethylethylenediamine (TMEDA)

H. Nakatsuji, Y. Tanabe, T. Misaki, 2006 .

Water-solvent method for tosylation and mesylation of primary alcohols promoted by KOH and catalytic amines

H. Nakatsuji, Y. Tanabe, T. Misaki, 2005 .

Mild, Powerful, and Robust Methods for Esterification, Amide Formation, and Thioesterification Between Acid Chlorides and Alcohols, Amines, Thiols, Respectively.

H. Nakatsuji, Y. Tanabe, M. Morimoto, 2008 .

Stereocomplementary Synthesis of cis- and trans-2-(p-Bromophenyl)-5-methylthiazolidin-4-ones: Useful Umpolung-type Suzuki–Miyaura Cross-coupling Partner and Donor

H. Nakatsuji, Y. Tanabe, Ryosuke Sasaki, 2018 .

“Phosphite–urea” cooperative high-turnover catalysts for the highly selective bromocyclization of homogeranylarenes

A. Sakakura, H. Nakatsuji, K. Ishihara, 2013 .

(E)- and (Z)-stereodefined enol phosphonates derived from β-ketoesters: stereocomplementary synthesis of fully-substituted α,β-unsaturated esters.

H. Hori, H. Nakatsuji, Y. Tanabe, 2015, Organic & biomolecular chemistry.

Cooperative activation with chiral nucleophilic catalysts and N-haloimides: enantioselective iodolactonization of 4-arylmethyl-4-pentenoic acids.

A. Sakakura, H. Nakatsuji, K. Ishihara, 2014, Angewandte Chemie.

Enantioselective aza-Friedel–Crafts reaction of furan with α-ketimino esters induced by a conjugated double hydrogen bond network of chiral bis(phosphoric acid) catalysts

A. Sakakura, H. Nakatsuji, K. Ishihara, 2018, Chemical science.

(Z )-Enol p -Tosylate Derived from Methyl Acetoacetate: A Useful Cross-Coupling Partner for the Synthesis of Methyl (Z )-3-Phenyl (or Aryl)-2-Butenoate

H. Nakatsuji, Y. Tanabe, Yuichiro Ashida, 2018, Organic Syntheses.

Straightforward Synthesis of N-Methyl-4-(pin)B-2(3H)-benzothiazol-2-one: A Promising Cross-Coupling Reagent

H. Nakatsuji, Y. Tanabe, Shotaro Izawa, 2018 .

Divergent Synthetic Access to E‐ and Z‐Stereodefined All‐Carbon‐Substituted Olefin Scaffolds: Application to Parallel Synthesis of (E)‐ and (Z)‐Tamoxifens

H. Nakatsuji, Y. Tanabe, Yuka Sato, 2017, ChemistryOpen.

(E)-,(Z)-parallel preparative methods for stereodefined β,β-diaryl- and α,β-diaryl-α,β-unsaturated esters: application to the stereocomplementary concise synthesis of zimelidine.

H. Nakatsuji, Y. Tanabe, Takeyuki Suzuki, 2015, Chemistry.

General, robust, and stereocomplementary preparation of alpha,beta-disubstituted alpha,beta-unsaturated esters.

H. Nakatsuji, Y. Tanabe, H. Nishikado, 2009, Organic letters.

General, robust, and stereocomplementary preparation of beta-ketoester enol tosylates as cross-coupling partners utilizing TsCl-N-methylimidazole agents.

H. Nakatsuji, Y. Tanabe, T. Misaki, 2008, Organic letters.

Acid–induced Favorskii–type Reaction: Regiocontrolled Elimination of Acyloin Mesylates Leading to α,β‐Unsaturated Ketones and Application to Formal Total Synthesis of (R)‐Muscone from Racemic Muscone

A. Tanaka, H. Nakatsuji, Y. Tanabe, 2016 .

Dehydration‐type Ti‐Claisen Condensation (Carbonhomologation) of α‐Heteroatom‐substituted Acetates with Alkyl Formates: Utilization as (Z)‐Stereodefined Cross‐coupling Partners and Application to Concise Synthesis of Strobilurin A

H. Nakatsuji, Y. Tanabe, Risako Kamada, 2017 .

Asymmetric Total Synthesis of (–)‐Azaspirene by Utilizing Ti‐Claisen Condensation and Ti‐Direct Aldol Reaction

H. Nakatsuji, Y. Tanabe, T. Misaki, 2016 .

Enantioselective bromocyclization of 2-geranylphenols induced by chiral phosphite-urea bifunctional catalysts.

A. Sakakura, H. Nakatsuji, K. Ishihara, 2016, Chemical communications.

Straightforward Synthesis of 2(5H)-Furanones as Promising Cross-Coupling Partners: Direct Furanone Annulation Utilizing Ti-Mediated Aldol Addition

H. Nakatsuji, Y. Tanabe, Yuichiro Ashida, 2016 .

Synthesis of unsymmetrically and highly substituted thiophenes utilizing regioselective ring-expansion of gem -dichlorocyclopropyl ketones with lawesson's reagent

H. Nakatsuji, Y. Tanabe, J. Motoyoshiya, 2007 .

Practical, general, and systematic method for optical resolution of gem-dihalo- and monohalocyclopropanecarboxylic acids utilizing chiral 1,1'-binaphtholmonomethyl ethers: application to the synthesis of three chiral pesticides.

E. Yoshida, A. Tanaka, H. Nakatsuji, 2008, Organic & biomolecular chemistry.

Synthesis of Unsymmetrically and Highly Substituted Thiophenes Utilizing Regioselective Ring‐Expansion of gem‐Dichlorocyclopropyl Ketones with Lawesson′s Reagent.

H. Nakatsuji, Y. Tanabe, J. Motoyoshiya, 2007 .

Enantioselective Halo-oxy- and Halo-azacyclizations Induced by Chiral Amidophosphate Catalysts and Halo-Lewis Acids.

H. Nakatsuji, K. Ishihara, Yanhui Lu, 2018, Journal of the American Chemical Society.

Selective bromocyclization of 2-geranylphenols promoted by phosphite-urea cooperative catalysts.

A. Sakakura, H. Nakatsuji, K. Ishihara, 2014, Chirality.

Asymmetric Total Syntheses of Two 3-Acyl-5,6-dihydro-2H-pyrones: (R)-Podoblastin-S and (R)-Lachnelluloic Acid with Verification of the Absolute Configuration of (−)-Lachnelluloic Acid

H. Nakatsuji, Y. Tanabe, Kohei Nakata, 2017, Molecules.

Reductive Ti-crossed Claisen Condensation between Methyl α-Bromocarboxylates and Acid Chlorides Utilizing a TiCl4–PPh3–N-Methylimidazole Reagent

A. Iida, H. Nakatsuji, Y. Tanabe, 2007 .

General, Robust, and Stereocomplementary Preparation of β-Ketoester Enol Tosylates as Cross-Coupling Partners Utilizing TsCl—N-Methylimidazole Agents.

H. Nakatsuji, Y. Tanabe, T. Misaki, 2008 .