Akai S - Search Results

1

Efficient lipase-catalyzed enantioselective desymmetrization of prochiral 2,2-disubstituted 1,3-propanediols and meso 1,2-diols using 1-ethoxyvinyl 2-furoate.

Akai S, Naka T, Fujita T, Takebe Y, Tsujino T, Kita Y. Akai S, et al. J Org Chem. 2002 Jan 25;67(2):411-9. doi: 10.1021/jo010587f. J Org Chem. 2002. PMID: 11798311

2

Synthetic anthracyclines: regiospecific total synthesis of D-ring thiophene analogues of daunomycin.

Kita Y, Kirihara M, Sekihachi J, Okunaka R, Sasho M, Mohri S, Honda T, Akai S, Tamura Y, Shimooka K. Kita Y, et al. Among authors: akai s. Chem Pharm Bull (Tokyo). 1990 Jul;38(7):1836-43. doi: 10.1248/cpb.38.1836. Chem Pharm Bull (Tokyo). 1990. PMID: 2268891

3

Convenient enzymatic resolution of alcohols using highly reactive, nonharmful acyl donors, 1-ethoxyvinyl esters.

Kita Y, Takebe Y, Murata K, Naka T, Akai S. Kita Y, et al. Among authors: akai s. J Org Chem. 2000 Jan 14;65(1):83-8. doi: 10.1021/jo9910785. J Org Chem. 2000. PMID: 10813899

4

An efficient synthesis of peri-hydroxy aromatic compounds via a strong-base-induced.

Iio K, Ramesh NG, Okajima A, Higuchi K, Fujioka H, Akai S, Kita Y. Iio K, et al. Among authors: akai s. J Org Chem. 2000 Jan 14;65(1):89-95. doi: 10.1021/jo990649q. J Org Chem. 2000. PMID: 10813900

5

Ambident effect of a p-sulfinyl group for the introduction of two carbon substituents to phenol rings: a convergent synthesis of diverse benzofuran neolignans.

Akai S, Morita N, Iio K, Nakamura Y, Kita Y. Akai S, et al. Org Lett. 2000 Jul 27;2(15):2279-82. doi: 10.1021/ol0001261. Org Lett. 2000. PMID: 10930263

6

Lipase-catalyzed asymmetric desymmetrization of prochiral 2,2-disubstituted 1,3-propanediols using 1-ethoxyvinyl benzoate.

Akai S, Naka T, Takebe Y, Kita Y. Akai S, et al. Chem Pharm Bull (Tokyo). 2000 Oct;48(10):1519-23. doi: 10.1248/cpb.48.1519. Chem Pharm Bull (Tokyo). 2000. PMID: 11045461

7

Total synthesis of the antitumor antibiotic (+/-)-fredericamycin A by a linear approach.

Kita Y, Iio K, Kawaguchi K, Fukuda N, Takeda Y, Ueno H, Okunaka R, Higuchi K, Tsujino T, Fujioka H, Akai S. Kita Y, et al. Among authors: akai s. Chemistry. 2000 Nov 3;6(21):3897-905. doi: 10.1002/1521-3765(20001103)6:21<3897::aid-chem3897>3.0.co;2-1. Chemistry. 2000. PMID: 11126950

8

Enantioselective total synthesis of a potent antitumor antibiotic, fredericamycin A.

Kita Y, Higuchi K, Yoshida Y, Iio K, Kitagaki S, Ueda K, Akai S, Fujioka H. Kita Y, et al. Among authors: akai s. J Am Chem Soc. 2001 Apr 11;123(14):3214-22. doi: 10.1021/ja0035699. J Am Chem Soc. 2001. PMID: 11457055

9

Enantiodivergent synthesis of either enantiomer of ABCDE-ring analogue of antitumor antibiotic fredericamycin A via intramolecular [4 + 2] cycloaddition approach.

Akai S, Tsujino T, Fukuda N, Iio K, Takeda Y, Kawaguchi Ki K, Naka T, Higuchi K, Kita Y. Akai S, et al. Org Lett. 2001 Dec 13;3(25):4015-8. doi: 10.1021/ol016696y. Org Lett. 2001. PMID: 11735573

10

Lipase-catalyzed domino kinetic resolution/intramolecular Diels-Alder reaction: one-pot synthesis of optically active 7-oxabicyclo[2.2.1]heptenes from furfuryl alcohols and beta-substituted acrylic acids.

Akai S, Naka T, Omura S, Tanimoto K, Imanishi M, Takebe Y, Matsugi M, Kita Y. Akai S, et al. Chemistry. 2002 Sep 16;8(18):4255-64. doi: 10.1002/1521-3765(20020916)8:18<4255::AID-CHEM4255>3.0.CO;2-6. Chemistry. 2002. PMID: 12298017

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