Iwabuchi Y - Search Results

1

Highly efficient aerobic oxidation of alcohols by using less-hindered nitroxyl-radical/copper catalysis: optimum catalyst combinations and their substrate scope.

Sasano Y, Kogure N, Nishiyama T, Nagasawa S, Iwabuchi Y. Sasano Y, et al. Among authors: iwabuchi y. Chem Asian J. 2015 Apr;10(4):1004-9. doi: 10.1002/asia.201403245. Epub 2015 Jan 23. Chem Asian J. 2015. PMID: 25620279

2

2-azaadamantane N-oxyl (AZADO) and 1-Me-AZADO: highly efficient organocatalysts for oxidation of alcohols.

Shibuya M, Tomizawa M, Suzuki I, Iwabuchi Y. Shibuya M, et al. Among authors: iwabuchi y. J Am Chem Soc. 2006 Jul 5;128(26):8412-3. doi: 10.1021/ja0620336. J Am Chem Soc. 2006. PMID: 16802802

3

Oxidative rearrangement of tertiary allylic alcohols employing oxoammonium salts.

Shibuya M, Tomizawa M, Iwabuchi Y. Shibuya M, et al. Among authors: iwabuchi y. J Org Chem. 2008 Jun 20;73(12):4750-2. doi: 10.1021/jo800634r. Epub 2008 May 24. J Org Chem. 2008. PMID: 18500838

4

Oxoammonium salt/NaClO2: an expedient, catalytic system for one-pot oxidation of primary alcohols to carboxylic acids with broad substrate applicability.

Shibuya M, Sato T, Tomizawa M, Iwabuchi Y. Shibuya M, et al. Among authors: iwabuchi y. Chem Commun (Camb). 2009 Apr 7;(13):1739-41. doi: 10.1039/b822944a. Epub 2009 Feb 11. Chem Commun (Camb). 2009. PMID: 19294280

5

Highly enantioselective organocatalytic oxidative kinetic resolution of secondary alcohols using chirally modified AZADOs.

Tomizawa M, Shibuya M, Iwabuchi Y. Tomizawa M, et al. Among authors: iwabuchi y. Org Lett. 2009 Apr 16;11(8):1829-31. doi: 10.1021/ol900441f. Org Lett. 2009. PMID: 19323487

6

An expeditious entry to 9-azabicyclo[3.3.1]nonane N-oxyl (ABNO): another highly active organocatalyst for oxidation of alcohols.

Shibuya M, Tomizawa M, Sasano Y, Iwabuchi Y. Shibuya M, et al. Among authors: iwabuchi y. J Org Chem. 2009 Jun 19;74(12):4619-22. doi: 10.1021/jo900486w. J Org Chem. 2009. PMID: 19476345

7

Highly efficient, organocatalytic aerobic alcohol oxidation.

Shibuya M, Osada Y, Sasano Y, Tomizawa M, Iwabuchi Y. Shibuya M, et al. Among authors: iwabuchi y. J Am Chem Soc. 2011 May 4;133(17):6497-500. doi: 10.1021/ja110940c. Epub 2011 Apr 7. J Am Chem Soc. 2011. PMID: 21473575

8

9-Azanoradamantane N-oxyl (Nor-AZADO): a highly active organocatalyst for alcohol oxidation.

Hayashi M, Sasano Y, Nagasawa S, Shibuya M, Iwabuchi Y. Hayashi M, et al. Among authors: iwabuchi y. Chem Pharm Bull (Tokyo). 2011;59(12):1570-3. doi: 10.1248/cpb.59.1570. Chem Pharm Bull (Tokyo). 2011. PMID: 22130384 Free article.

9

Oxidation of alcohols to carbonyl compounds with diisopropyl azodicarboxylate catalyzed by nitroxyl radicals.

Hayashi M, Shibuya M, Iwabuchi Y. Hayashi M, et al. Among authors: iwabuchi y. J Org Chem. 2012 Mar 16;77(6):3005-9. doi: 10.1021/jo300088b. Epub 2012 Feb 29. J Org Chem. 2012. PMID: 22352461

10

Organocatalytic one-pot oxidative cleavage of terminal diols to dehomologated carboxylic acids.

Shibuya M, Doi R, Shibuta T, Uesugi S, Iwabuchi Y. Shibuya M, et al. Among authors: iwabuchi y. Org Lett. 2012 Oct 5;14(19):5006-9. doi: 10.1021/ol3021429. Epub 2012 Sep 19. Org Lett. 2012. PMID: 22991924

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