Odagi M - Search Results

1

Synthetic studies of (23S,25R)-1α,25-dihydroxyvitamin D₃ 26,23-lactone (calcitriol lactone) and its derivatives.

Akagi Y, Nagata A, Odagi M, Nagasawa K. Akagi Y, et al. Among authors: odagi m. J Steroid Biochem Mol Biol. 2018 Mar;177:240-246. doi: 10.1016/j.jsbmb.2017.07.017. Epub 2017 Jul 27. J Steroid Biochem Mol Biol. 2018. PMID: 28757443 Review.

2

Asymmetric α-hydroxylation of tetralone-derived β-ketoesters by using a guanidine-urea bifunctional organocatalyst in the presence of cumene hydroperoxide.

Odagi M, Furukori K, Watanabe T, Nagasawa K. Odagi M, et al. Chemistry. 2013 Dec 2;19(49):16740-5. doi: 10.1002/chem.201303006. Epub 2013 Nov 4. Chemistry. 2013. PMID: 24281815

3

Asymmetric α-hydroxylation of a lactone with vinylogous pyridone by using a guanidine-urea bifunctional organocatalyst: catalytic enantioselective synthesis of a key intermediate for (20S)-camptothecin analogues.

Watanabe T, Odagi M, Furukori K, Nagasawa K. Watanabe T, et al. Among authors: odagi m. Chemistry. 2014 Jan 7;20(2):591-7. doi: 10.1002/chem.201303633. Epub 2013 Nov 28. Chemistry. 2014. PMID: 24288205

4

Origin of stereocontrol in guanidine-bisurea bifunctional organocatalyst that promotes α-hydroxylation of tetralone-derived β-ketoesters: asymmetric synthesis of β- and γ-substituted tetralone derivatives via organocatalytic oxidative kinetic resolution.

Odagi M, Furukori K, Yamamoto Y, Sato M, Iida K, Yamanaka M, Nagasawa K. Odagi M, et al. J Am Chem Soc. 2015 Feb 11;137(5):1909-15. doi: 10.1021/ja511149y. Epub 2015 Jan 29. J Am Chem Soc. 2015. PMID: 25580909

5

Development of Guanidine-Bisurea Bifunctional Organocatalysts with a Chiral Pyrrolidine Moiety and Application to α-Hydroxylation of Tetralone-Derived β-Keto Esters.

Odagi M, Takayama K, Sato M, Yamanaka M, Nagasawa K. Odagi M, et al. Molecules. 2015 Jul 10;20(7):12590-8. doi: 10.3390/molecules200712590. Molecules. 2015. PMID: 26184142 Free PMC article.

6

Asymmetric α-amination of β-keto esters using a guanidine-bisurea bifunctional organocatalyst.

Odagi M, Yamamoto Y, Nagasawa K. Odagi M, et al. Beilstein J Org Chem. 2016 Feb 4;12:198-203. doi: 10.3762/bjoc.12.22. eCollection 2016. Beilstein J Org Chem. 2016. PMID: 26977179 Free PMC article.

7

Total Synthesis of Rishirilide B by Organocatalytic Oxidative Kinetic Resolution: Revision of Absolute Configuration of (+)-Rishirilide B.

Odagi M, Furukori K, Takayama K, Noguchi K, Nagasawa K. Odagi M, et al. Angew Chem Int Ed Engl. 2017 Jun 1;56(23):6609-6612. doi: 10.1002/anie.201701431. Epub 2017 May 4. Angew Chem Int Ed Engl. 2017. PMID: 28471011

8

Total Synthesis of (+)-Gracilamine Based on an Oxidative Phenolic Coupling Reaction and Determination of Its Absolute Configuration.

Odagi M, Yamamoto Y, Nagasawa K. Odagi M, et al. Angew Chem Int Ed Engl. 2018 Feb 19;57(8):2229-2232. doi: 10.1002/anie.201708575. Epub 2017 Oct 11. Angew Chem Int Ed Engl. 2018. PMID: 28929558

9

Targeting STUB1-tissue factor axis normalizes hyperthrombotic uremic phenotype without increasing bleeding risk.

Shashar M, Belghasem ME, Matsuura S, Walker J, Richards S, Alousi F, Rijal K, Kolachalama VB, Balcells M, Odagi M, Nagasawa K, Henderson JM, Gautam A, Rushmore R, Francis J, Kirchhofer D, Kolandaivelu K, Sherr DH, Edelman ER, Ravid K, Chitalia VC. Shashar M, et al. Among authors: odagi m. Sci Transl Med. 2017 Nov 22;9(417):eaam8475. doi: 10.1126/scitranslmed.aam8475. Sci Transl Med. 2017. PMID: 29167396 Free PMC article.

10

Synthesis of 2,6,7-Trisubstituted Prenylated indole.

Shiozawa M, Iida K, Odagi M, Yamanaka M, Nagasawa K. Shiozawa M, et al. Among authors: odagi m. J Org Chem. 2018 Jul 6;83(13):7276-7280. doi: 10.1021/acs.joc.7b03273. Epub 2018 Mar 14. J Org Chem. 2018. PMID: 29516739

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