Ohno H - Search Results

1

Design of Synthetic Surrogates for the Macrolactone Linker Motif in Coibamide A.

Suzuki R, Mattos DR, Kitamura T, Tsujioka R, Kobayashi K, Inuki S, Ohno H, Ishmael JE, McPhail KL, Oishi S. Suzuki R, et al. Among authors: ohno h. ACS Med Chem Lett. 2023 Sep 19;14(10):1344-1350. doi: 10.1021/acsmedchemlett.3c00232. eCollection 2023 Oct 12. ACS Med Chem Lett. 2023. PMID: 37849553 Free PMC article.

2

Synthesis of allenes from allylic alcohol derivatives bearing a bromine atom using a palladium(0)/diethylzinc system.

Ohno H, Miyamura K, Tanaka T, Oishi S, Toda A, Takemoto Y, Fujii N, Ibuka T. Ohno H, et al. J Org Chem. 2002 Feb 22;67(4):1359-67. doi: 10.1021/jo016320y. J Org Chem. 2002. PMID: 11846687

3

Stereoselective synthesis of 3,6-disubstituted-3,6-dihydropyridin-2-ones as potential diketopiperazine mimetics using organocopper-mediated anti-SN2' reactions and their use in the preparation of low-molecule CXCR4 antagonists.

Niida A, Tanigaki H, Inokuchi E, Sasaki Y, Oishi S, Ohno H, Tamamura H, Wang Z, Peiper SC, Kitaura K, Otaka A, Fujii N. Niida A, et al. Among authors: ohno h. J Org Chem. 2006 May 12;71(10):3942-51. doi: 10.1021/jo060390t. J Org Chem. 2006. PMID: 16674071

4

Synthesis of (Z)-alkene and (E)-fluoroalkene-containing diketopiperazine mimetics utilizing organocopper-mediated reduction-alkylation and diastereoselectivity examination using DFT calculations.

Niida A, Mizumoto M, Narumi T, Inokuchi E, Oishi S, Ohno H, Otaka A, Kitaura K, Fujii N. Niida A, et al. Among authors: ohno h. J Org Chem. 2006 May 26;71(11):4118-29. doi: 10.1021/jo060202z. J Org Chem. 2006. PMID: 16709051

5

Structure-activity relationship study on small peptidic GPR54 agonists.

Tomita K, Niida A, Oishi S, Ohno H, Cluzeau J, Navenot JM, Wang ZX, Peiper SC, Fujii N. Tomita K, et al. Among authors: ohno h. Bioorg Med Chem. 2006 Nov 15;14(22):7595-603. doi: 10.1016/j.bmc.2006.07.009. Epub 2006 Aug 1. Bioorg Med Chem. 2006. PMID: 16879969

6

A novel one-pot reaction involving organocopper-mediated reduction/transmetalation/asymmetric alkylation, leading to the diastereoselective synthesis of functionalized (Z)-fluoroalkene dipeptide isosteres.

Narumi T, Niida A, Tomita K, Oishi S, Otaka A, Ohno H, Fujii N. Narumi T, et al. Among authors: ohno h. Chem Commun (Camb). 2006 Dec 7;(45):4720-2. doi: 10.1039/b608596b. Epub 2006 Sep 28. Chem Commun (Camb). 2006. PMID: 17109048

7

Fmoc-based solid-phase synthesis of GPR54-agonistic pentapeptide derivatives containing alkene- and fluoroalkene-dipeptide isosteres.

Tomita K, Narumi T, Niida A, Oishi S, Ohno H, Fujii N. Tomita K, et al. Among authors: ohno h. Biopolymers. 2007;88(2):272-8. doi: 10.1002/bip.20676. Biopolymers. 2007. PMID: 17216632

8

Structure-activity relationships of cyclic peptide-based chemokine receptor CXCR4 antagonists: disclosing the importance of side-chain and backbone functionalities.

Ueda S, Oishi S, Wang ZX, Araki T, Tamamura H, Cluzeau J, Ohno H, Kusano S, Nakashima H, Trent JO, Peiper SC, Fujii N. Ueda S, et al. Among authors: ohno h. J Med Chem. 2007 Jan 25;50(2):192-8. doi: 10.1021/jm0607350. J Med Chem. 2007. PMID: 17228861

9

Direct synthesis of 2-(aminomethyl)indoles through copper(I)-catalyzed domino three-component coupling and cyclization reactions.

Ohno H, Ohta Y, Oishi S, Fujii N. Ohno H, et al. Angew Chem Int Ed Engl. 2007;46(13):2295-8. doi: 10.1002/anie.200604342. Angew Chem Int Ed Engl. 2007. PMID: 17300118 No abstract available.

10

Design and synthesis of all diastereomers of cyclic pseudo-dipeptides as mimics of cyclic CXCR4 pentapeptide antagonists.

Cluzeau J, Oishi S, Ohno H, Wang Z, Evans B, Peiper SC, Fujii N. Cluzeau J, et al. Among authors: ohno h. Org Biomol Chem. 2007 Jun 21;5(12):1915-23. doi: 10.1039/b702649h. Epub 2007 May 14. Org Biomol Chem. 2007. PMID: 17551641

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