Lin GQ - Search Results

1

Design of C2-symmetric tetrahydropentalenes as new chiral diene ligands for highly enantioselective Rh-catalyzed arylation of N-tosylarylimines with arylboronic acids.

Wang ZQ, Feng CG, Xu MH, Lin GQ. Wang ZQ, et al. Among authors: lin gq. J Am Chem Soc. 2007 May 2;129(17):5336-7. doi: 10.1021/ja0710914. Epub 2007 Apr 11. J Am Chem Soc. 2007. PMID: 17425322 No abstract available.

2

A highly efficient asymmetric synthesis of optically active alpha, gamma-substituted gamma-butyrolactones using a chiral auxiliary derived from isosorbide.

Xu MH, Wang W, Lin GQ. Xu MH, et al. Among authors: lin gq. Org Lett. 2000 Jul 27;2(15):2229-32. doi: 10.1021/ol005978f. Org Lett. 2000. PMID: 10930250

3

Development of a new reaction system for the synthesis of highly optically active alpha,gamma-substituted gamma-butyrolactones.

Xu MH, Wang W, Xia LJ, Lin GQ. Xu MH, et al. Among authors: lin gq. J Org Chem. 2001 Jun 1;66(11):3953-62. doi: 10.1021/jo0155153. J Org Chem. 2001. PMID: 11375020

4

Samarium diiodide-induced asymmetric synthesis of optically pure unsymmetrical vicinal diamines by reductive cross-coupling of nitrones with N-tert-butanesulfinyl imines.

Zhong YW, Xu MH, Lin GQ. Zhong YW, et al. Among authors: lin gq. Org Lett. 2004 Oct 28;6(22):3953-6. doi: 10.1021/ol048444d. Org Lett. 2004. PMID: 15496072

5

Highly diastereoselective and enantioselective synthesis of enantiopure C2-Symmetrical vicinal diamines by reductive homocoupling of chiral N-tert-butanesulfinyl imines.

Zhong YW, Izumi K, Xu MH, Lin GQ. Zhong YW, et al. Among authors: lin gq. Org Lett. 2004 Dec 9;6(25):4747-50. doi: 10.1021/ol0479803. Org Lett. 2004. PMID: 15575676

6

A new entry to asymmetric synthesis of optically active alpha,gamma-substituted gamma-butyrolactones, using a carbohydrate derived amide as both a chiral auxiliary and a proton source.

Huang LL, Xu MH, Lin GQ. Huang LL, et al. Among authors: lin gq. J Org Chem. 2005 Jan 21;70(2):529-32. doi: 10.1021/jo0485637. J Org Chem. 2005. PMID: 15651797

7

A highly efficient and direct approach for synthesis of enantiopure beta-amino alcohols by reductive cross-coupling of chiral N-tert-butanesulfinyl imines with aldehydes.

Zhong YW, Dong YZ, Fang K, Izumi K, Xu MH, Lin GQ. Zhong YW, et al. Among authors: lin gq. J Am Chem Soc. 2005 Aug 31;127(34):11956-7. doi: 10.1021/ja054401w. J Am Chem Soc. 2005. PMID: 16117531

8

Catalytic enantioselective synthesis of chiral phthalides by SmI2-mediated reductive cyclization of 2-acylarylcarboxylates.

Huang LL, Xu MH, Lin GQ. Huang LL, et al. Among authors: lin gq. J Am Chem Soc. 2006 May 3;128(17):5624-5. doi: 10.1021/ja061114z. J Am Chem Soc. 2006. PMID: 16637615

9

Room-temperature highly diastereoselective Zn-mediated allylation of chiral N-tert-butanesulfinyl imines: remarkable reaction condition controlled stereoselectivity reversal.

Sun XW, Xu MH, Lin GQ. Sun XW, et al. Among authors: lin gq. Org Lett. 2006 Oct 12;8(21):4979-82. doi: 10.1021/ol062216x. Org Lett. 2006. PMID: 17020351

10

Remarkable salt effect on In-mediated allylation of N-tert-butanesulfinyl imines in aqueous media: highly practical asymmetric synthesis of chiral homoallylic amines and isoindolinones.

Sun XW, Liu M, Xu MH, Lin GQ. Sun XW, et al. Among authors: lin gq. Org Lett. 2008 Mar 20;10(6):1259-62. doi: 10.1021/ol8001514. Epub 2008 Feb 15. Org Lett. 2008. PMID: 18275212

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