Da CS - Search Results

1

Pd(II)-Catalyzed C4-Selective Alkynylation of Indoles by a Transient Directing Group.

Zhang ZX, Zhang B, Yuan M, Zhao PF, Da CS. Zhang ZX, et al. Among authors: da cs. Org Lett. 2024 Aug 16;26(32):6819-6824. doi: 10.1021/acs.orglett.4c01970. Epub 2024 Aug 6. Org Lett. 2024. PMID: 39106047

2

Highly asymmetric aldol reaction of isatins and ketones catalyzed by chiral bifunctional primary-amine organocatalyst on water.

Lv XX, Liu N, Chen F, Zhang H, Du ZH, Wang P, Yuan M, Da CS. Lv XX, et al. Among authors: da cs. Org Biomol Chem. 2023 Nov 8;21(43):8695-8701. doi: 10.1039/d3ob01227a. Org Biomol Chem. 2023. PMID: 37861676

3

Rh(III)-Catalyzed Dual C-H Functionalization and C-O/C-N Annulations of Monoamide Fumarates.

Han ZJ, Zhang ZX, Lin JJ, Ma B, Yang LX, Pu WG, Li YM, Chen H, Da CS. Han ZJ, et al. Among authors: da cs. J Org Chem. 2022 Nov 18;87(22):15547-15558. doi: 10.1021/acs.joc.2c02091. Epub 2022 Oct 28. J Org Chem. 2022. PMID: 36306342

4

Highly enantioselective one-pot sequential synthesis of valerolactones and pyrazolones bearing all-carbon quaternary stereocentres.

Xu YL, Qin ZZ, Wang YX, Zhao PF, Li HF, Du ZH, Da CS. Xu YL, et al. Among authors: da cs. Org Biomol Chem. 2021 Feb 25;19(7):1610-1615. doi: 10.1039/d0ob02489a. Org Biomol Chem. 2021. PMID: 33528484

5

Correction: N-Primary-amine tetrapeptide-catalyzed highly asymmetric Michael addition of aliphatic aldehydes to maleimides.

Du ZH, Qin WJ, Tao BX, Yuan M, Da CS. Du ZH, et al. Among authors: da cs. Org Biomol Chem. 2020 Nov 25;18(45):9317. doi: 10.1039/d0ob90155e. Org Biomol Chem. 2020. PMID: 33179697

6

N-Primary-amine tetrapeptide-catalyzed highly asymmetric Michael addition of aliphatic aldehydes to maleimides.

Du ZH, Qin WJ, Tao BX, Yuan M, Da CS. Du ZH, et al. Among authors: da cs. Org Biomol Chem. 2020 Sep 21;18(35):6899-6904. doi: 10.1039/d0ob01457e. Epub 2020 Aug 28. Org Biomol Chem. 2020. PMID: 32856662

7

Peptide-Catalyzed Highly Asymmetric Cross-Aldol Reaction of Aldehydes to Biomimetically Synthesize 1,4-Dicarbonyls.

Du ZH, Tao BX, Yuan M, Qin WJ, Xu YL, Wang P, Da CS. Du ZH, et al. Among authors: da cs. Org Lett. 2020 Jun 5;22(11):4444-4450. doi: 10.1021/acs.orglett.0c01407. Epub 2020 May 28. Org Lett. 2020. PMID: 32463241

8

Enantioselective vinylation of aldehydes with the vinyl Grignard reagent catalyzed by magnesium complex of chiral BINOLs.

Wang P, Ma GR, Yu SL, Da CS. Wang P, et al. Among authors: da cs. Chirality. 2019 Jan;31(1):79-86. doi: 10.1002/chir.23038. Epub 2018 Dec 6. Chirality. 2019. PMID: 30520127

9

Correction to "Organocatalytic Enantioselective Cross-Aldol Reaction of o-Hydroxyarylketones and Trifluoromethyl Ketones".

Wang P, Li HF, Zhao JZ, Du ZH, Da CS. Wang P, et al. Among authors: da cs. Org Lett. 2018 Jan 19;20(2):497. doi: 10.1021/acs.orglett.7b03805. Epub 2017 Dec 13. Org Lett. 2018. PMID: 29235869 No abstract available.

10

The inexpensive additive N-methylmorpholine effectively decreases the equivalents of nucleophiles in the catalytic highly enantioselective arylation of aryl aldehydes.

Wang P, Liu Y, Zhang YL, Da CS. Wang P, et al. Among authors: da cs. Chirality. 2017 Aug;29(8):443-450. doi: 10.1002/chir.22709. Epub 2017 May 25. Chirality. 2017. PMID: 28543685

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