Sun J - Search Results

1

An organocatalyst bearing stereogenic carbon and sulfur centers as an efficient promoter for enantioselective hydrosilylation of 1,4-benzooxazines.

Liu XW, Wang C, Yan Y, Wang YQ, Sun J. Liu XW, et al. Among authors: sun j. J Org Chem. 2013 Jun 21;78(12):6276-80. doi: 10.1021/jo400187e. Epub 2013 Jun 11. J Org Chem. 2013. PMID: 23718757

2

Highly enantioselective reduction of β-amino nitroolefins with a simple N-sulfinyl urea as bifunctional catalyst.

Liu XW, Yan Y, Wang YQ, Wang C, Sun J. Liu XW, et al. Among authors: sun j. Chemistry. 2012 Jul 23;18(30):9204-7. doi: 10.1002/chem.201201192. Epub 2012 Jun 26. Chemistry. 2012. PMID: 22736502

3

L-Pipecolinic acid derived Lewis base organocatalyst for asymmetric reduction of N-aryl imines by trichlorosilane: effects of the side amide group on catalytic performances.

Wang Z, Wang C, Zhou L, Sun J. Wang Z, et al. Among authors: sun j. Org Biomol Chem. 2013 Feb 7;11(5):787-97. doi: 10.1039/c2ob26772a. Epub 2012 Dec 7. Org Biomol Chem. 2013. PMID: 23223869

4

One-pot formation of chiral polysubstituted 3,4-dihydropyrans via a novel organocatalytic domino sequence involving alkynal self-condensation.

Dong LJ, Fan TT, Wang C, Sun J. Dong LJ, et al. Among authors: sun j. Org Lett. 2013 Jan 4;15(1):204-7. doi: 10.1021/ol3032285. Epub 2012 Dec 21. Org Lett. 2013. PMID: 23259735

5

L-Valine derived chiral N-sulfinamides as effective organocatalysts for the asymmetric hydrosilylation of N-alkyl and N-aryl protected ketimines.

Wang C, Wu X, Zhou L, Sun J. Wang C, et al. Among authors: sun j. Org Biomol Chem. 2015 Jan 14;13(2):577-82. doi: 10.1039/c4ob01257g. Epub 2014 Nov 7. Org Biomol Chem. 2015. PMID: 25380100

6

Reductive Hydrazination with Trichlorosilane: A Method for the Preparation of 1,1-Disubstituted Hydrazines.

Wang T, Di X, Wang C, Zhou L, Sun J. Wang T, et al. Among authors: sun j. Org Lett. 2016 Apr 15;18(8):1900-3. doi: 10.1021/acs.orglett.6b00675. Epub 2016 Apr 6. Org Lett. 2016. PMID: 27049166

7

Protonated N'-benzyl-N'-prolyl proline hydrazide as highly enantioselective catalyst for direct asymmetric aldol reaction.

Cheng C, Sun J, Wang C, Zhang Y, Wei S, Jiang F, Wu Y. Cheng C, et al. Among authors: sun j. Chem Commun (Camb). 2006 Jan 14;(2):215-7. doi: 10.1039/b511992h. Epub 2005 Nov 18. Chem Commun (Camb). 2006. PMID: 16372110

8

A highly enantioselective organocatalytic method for reduction of aromatic N-alkyl ketimines.

Wang C, Wu X, Zhou L, Sun J. Wang C, et al. Among authors: sun j. Chemistry. 2008;14(29):8789-8792. doi: 10.1002/chem.200801479. Chemistry. 2008. PMID: 18752235 Free article. No abstract available.

9

Chiral Lewis base catalyzed highly enantioselective reduction of N-alkyl β-enamino esters with trichlorosilane and water.

Wu X, Li Y, Wang C, Zhou L, Lu X, Sun J. Wu X, et al. Among authors: sun j. Chemistry. 2011 Mar 1;17(10):2846-8. doi: 10.1002/chem.201003105. Epub 2011 Feb 10. Chemistry. 2011. PMID: 21312301 No abstract available.

10

Direct asymmetric hydrosilylation of indoles: combined Lewis base and Brønsted acid activation.

Xiao YC, Wang C, Yao Y, Sun J, Chen YC. Xiao YC, et al. Among authors: sun j. Angew Chem Int Ed Engl. 2011 Nov 4;50(45):10661-4. doi: 10.1002/anie.201105341. Epub 2011 Sep 20. Angew Chem Int Ed Engl. 2011. PMID: 21932274 No abstract available.

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