Hidefumi Nakatsuji - Search Results

Year	Number of Results
2007	1
2008	2
2009	1
2014	2
2015	2
2016	1
2017	2
2018	2
2023	0

1

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

Sawamura Y, Ogura Y, Nakatsuji H, Sakakura A, Ishihara K. Sawamura Y, et al. Among authors: nakatsuji h. Chem Commun (Camb). 2016 May 4;52(36):6068-71. doi: 10.1039/c6cc00229c. Epub 2016 Mar 29. Chem Commun (Camb). 2016. PMID: 27020117

2

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

Nakatsuji H, Sawamura Y, Sakakura A, Ishihara K. Nakatsuji H, et al. Angew Chem Int Ed Engl. 2014 Jul 1;53(27):6974-7. doi: 10.1002/anie.201400946. Epub 2014 May 19. Angew Chem Int Ed Engl. 2014. PMID: 24840957

3

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

Lu Y, Nakatsuji H, Okumura Y, Yao L, Ishihara K. Lu Y, et al. Among authors: nakatsuji h. J Am Chem Soc. 2018 May 16;140(19):6039-6043. doi: 10.1021/jacs.8b02607. Epub 2018 May 7. J Am Chem Soc. 2018. PMID: 29708750

4

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

Sawamura Y, Nakatsuji H, Akakura M, Sakakura A, Ishihara K. Sawamura Y, et al. Among authors: nakatsuji h. Chirality. 2014 Jul;26(7):356-60. doi: 10.1002/chir.22297. Epub 2014 Feb 7. Chirality. 2014. PMID: 24526498

5

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.

Fujiwara T, Tsutsumi T, Nakata K, Nakatsuji H, Tanabe Y. Fujiwara T, et al. Among authors: nakatsuji h. Molecules. 2017 Jan 1;22(1):69. doi: 10.3390/molecules22010069. Molecules. 2017. PMID: 28045445 Free PMC article.

6

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.

Yasukochi H, Atago T, Tanaka A, Nakatsuji H, Yoshida E, Kakehi A, Nishii Y, Tanabe Y. Yasukochi H, et al. Among authors: nakatsuji h. Org Biomol Chem. 2008 Feb 7;6(3):540-7. doi: 10.1039/b714614k. Epub 2007 Dec 18. Org Biomol Chem. 2008. PMID: 18219425

7

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

Nakatsuji H, Nishikado H, Ueno K, Tanabe Y. Nakatsuji H, et al. Org Lett. 2009 Oct 1;11(19):4258-61. doi: 10.1021/ol9013359. Org Lett. 2009. PMID: 19715286

8

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

Nakatsuji H, Ashida Y, Hori H, Sato Y, Honda A, Taira M, Tanabe Y. Nakatsuji H, et al. Org Biomol Chem. 2015 Aug 14;13(30):8205-10. doi: 10.1039/c5ob01097g. Org Biomol Chem. 2015. PMID: 26133291

9

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.

Hatano M, Okamoto H, Kawakami T, Toh K, Nakatsuji H, Sakakura A, Ishihara K. Hatano M, et al. Among authors: nakatsuji h. Chem Sci. 2018 Jun 25;9(30):6361-6367. doi: 10.1039/c8sc02290a. eCollection 2018 Aug 14. Chem Sci. 2018. PMID: 30288231 Free PMC article.

10

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

Nakatsuji H, Ueno K, Misaki T, Tanabe Y. Nakatsuji H, et al. Org Lett. 2008 Jun 5;10(11):2131-4. doi: 10.1021/ol800480d. Epub 2008 May 9. Org Lett. 2008. PMID: 18465867

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