Sun J - Search Results

1

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

2

Evolution of chiral Lewis basic N-formamide as highly effective organocatalyst for asymmetric reduction of both ketones and ketimines with an unprecedented substrate scope.

Zhou L, Wang Z, Wei S, Sun J. Zhou L, et al. Among authors: sun j. Chem Commun (Camb). 2007 Jul 28;(28):2977-9. doi: 10.1039/b703307a. Epub 2007 May 9. Chem Commun (Camb). 2007. PMID: 17622450

3

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

4

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

5

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

6

A highly enantioselective lewis basic organocatalyst for reduction of N-aryl imines with unprecedented substrate spectrum.

Wang Z, Ye X, Wei S, Wu P, Zhang A, Sun J. Wang Z, et al. Among authors: sun j. Org Lett. 2006 Mar 2;8(5):999-1001. doi: 10.1021/ol060112g. Org Lett. 2006. PMID: 16494494

7

l-Piperazine-2-carboxylic acid derived N-formamide as a highly enantioselective Lewis basic catalyst for hydrosilylation of N-aryl imines with an unprecedented substrate profile.

Wang Z, Cheng M, Wu P, Wei S, Sun J. Wang Z, et al. Among authors: sun j. Org Lett. 2006 Jul 6;8(14):3045-8. doi: 10.1021/ol060984i. Org Lett. 2006. PMID: 16805548

8

S-chiral sulfinamides as highly enantioselective organocatalysts.

Pei D, Wang Z, Wei S, Zhang Y, Sun J. Pei D, et al. Among authors: sun j. Org Lett. 2006 Dec 7;8(25):5913-5. doi: 10.1021/ol062633+. Org Lett. 2006. PMID: 17134304

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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