Kobayashi S - Search Results

1

Development of Continuous-Flow Reactions for the Synthesis of Anti-Alzheimer Drug Memantine.

Iwata M, Furiya Y, Ishitani H, Kobayashi S. Iwata M, et al. Among authors: kobayashi s. Chemistry. 2024 Nov 29:e202403562. doi: 10.1002/chem.202403562. Online ahead of print. Chemistry. 2024. PMID: 39611355

2

Highly anti-selective asymmetric aldol reactions using chiral zirconium catalysts. Improvement of activities, structure of the novel zirconium complexes, and effect of a small amount of water for the preparation of the catalysts.

Yamashita Y, Ishitani H, Shimizu H, Kobayashi S. Yamashita Y, et al. Among authors: kobayashi s. J Am Chem Soc. 2002 Apr 3;124(13):3292-302. doi: 10.1021/ja016293t. J Am Chem Soc. 2002. PMID: 11916413

3

Catalytic, asymmetric trans-selective hetero Diels-Alder reactions using a chiral zirconium complex.

Yamashita Y, Saito S, Ishitani H, Kobayashi S. Yamashita Y, et al. Among authors: kobayashi s. Org Lett. 2002 Apr 4;4(7):1221-3. doi: 10.1021/ol025745j. Org Lett. 2002. PMID: 11922823

4

Catalytic asymmetric carbon-carbon bond-forming reactions in aqueous media.

Manabe K, Kobayashi S. Manabe K, et al. Among authors: kobayashi s. Chemistry. 2002 Sep 16;8(18):4094-101. doi: 10.1002/1521-3765(20020916)8:18<4094::AID-CHEM4094>3.0.CO;2-G. Chemistry. 2002. PMID: 12297999

5

Catalytic enantioselective addition of propionate units to imines: an efficient synthesis of anti-alpha-methyl-beta-amino acid derivatives.

Kobayashi S, Kobayashi J, Ishitani H, Ueno M. Kobayashi S, et al. Among authors: kobayashi j. Chemistry. 2002 Sep 16;8(18):4185-90. doi: 10.1002/1521-3765(20020916)8:18<4185::AID-CHEM4185>3.0.CO;2-6. Chemistry. 2002. PMID: 12298008

6

Air-stable, storable, and highly selective chiral Lewis acid catalyst.

Ueno M, Ishitani H, Kobayashi S. Ueno M, et al. Among authors: kobayashi s. Org Lett. 2002 Oct 3;4(20):3395-7. doi: 10.1021/ol026452t. Org Lett. 2002. PMID: 12323027

7

Asymmetric intramolecular [3 + 2] cycloaddition reactions of acylhydrazones/olefins using a chiral zirconium catalyst.

Kobayashi S, Shimizu H, Yamashita Y, Ishitani H, Kobayashi J. Kobayashi S, et al. Among authors: kobayashi j. J Am Chem Soc. 2002 Nov 20;124(46):13678-9. doi: 10.1021/ja027681d. J Am Chem Soc. 2002. PMID: 12431089

8

Chiral hetero Diels-Alder products by enantioselective and diastereoselective zirconium catalysis. Scope, limitation, mechanism, and application to the concise synthesis of (+)-Prelactone C and (+)-9-deoxygoniopypyrone.

Yamashita Y, Saito S, Ishitani H, Kobayashi S. Yamashita Y, et al. Among authors: kobayashi s. J Am Chem Soc. 2003 Apr 2;125(13):3793-8. doi: 10.1021/ja028186k. J Am Chem Soc. 2003. PMID: 12656612

9

Air-stable, storable, and highly efficient chiral zirconium catalysts for enantioselective Mannich-type, aza Diels-Alder, aldol, and hetero Diels-Alder reactions.

Kobayashi S, Ueno M, Saito S, Mizuki Y, Ishitani H, Yamashita Y. Kobayashi S, et al. Proc Natl Acad Sci U S A. 2004 Apr 13;101(15):5476-81. doi: 10.1073/pnas.0307870101. Epub 2004 Apr 5. Proc Natl Acad Sci U S A. 2004. PMID: 15067139 Free PMC article.

10

A novel dinuclear chiral niobium complex for Lewis acid catalyzed enantioselective reactions: design of a tridentate ligand and elucidation of the catalyst structure.

Kobayashi S, Arai K, Shimizu H, Ihori Y, Ishitani H, Yamashita Y. Kobayashi S, et al. Angew Chem Int Ed Engl. 2005 Jan 21;44(5):761-4. doi: 10.1002/anie.200462204. Angew Chem Int Ed Engl. 2005. PMID: 15612063 No abstract available.

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