Jiang Y - Search Results

1

Enantioselective cyanosilylation of ketones by a catalytic double-activation method with an aluminium complex and an N-oxide.

Chen FX, Zhou H, Liu X, Qin B, Feng X, Zhang G, Jiang Y. Chen FX, et al. Among authors: jiang y. Chemistry. 2004 Oct 4;10(19):4790-7. doi: 10.1002/chem.200400506. Chemistry. 2004. PMID: 15372678

2

Enantioselective cyanosilylation of ketones by a catalytic double-activation method employing chiral Lewis acid and achiral N-oxide catalysts.

Chen F, Feng X, Qin B, Zhang G, Jiang Y. Chen F, et al. Among authors: jiang y. Org Lett. 2003 Mar 20;5(6):949-52. doi: 10.1021/ol034158a. Org Lett. 2003. PMID: 12633113 Free article.

3

A highly enantioselective hetero-Diels-Alder reaction of aldehydes with Danishefsky's diene catalyzed by chiral titanium(IV) 5,5',6,6',7,7',8,8'-octahydro-1,1'-bi-2-naphthol complexes.

Wang B, Feng X, Huang Y, Liu H, Cui X, Jiang Y. Wang B, et al. Among authors: jiang y. J Org Chem. 2002 Apr 5;67(7):2175-82. doi: 10.1021/jo016240u. J Org Chem. 2002. PMID: 11925225

4

Modification of (1R,2S)-1,2-diphenyl-2-aminoethanol for the highly enantioselective, asymmetric alkylation of N-diphenylphosphinoyl arylimines with dialkylzinc.

Zhang HL, Jiang F, Zhang XM, Cui X, Gong LZ, Mi AQ, Jiang YZ, Wu YD. Zhang HL, et al. Chemistry. 2004 Mar 19;10(6):1481-92. doi: 10.1002/chem.200305418. Chemistry. 2004. PMID: 15034892

5

Organocatalyzed highly enantioselective direct aldol reactions of aldehydes with hydroxyacetone and fluoroacetone in aqueous media: the use of water to control regioselectivity.

Chen XH, Luo SW, Tang Z, Cun LF, Mi AQ, Jiang YZ, Gong LZ. Chen XH, et al. Chemistry. 2007;13(2):689-701. doi: 10.1002/chem.200600801. Chemistry. 2007. PMID: 17013967

6

Design of highly enantioselective organocatalysts based on molecular recognition.

Tang Z, Cun LF, Cui X, Mi AQ, Jiang YZ, Gong LZ. Tang Z, et al. Org Lett. 2006 Mar 30;8(7):1263-6. doi: 10.1021/ol0529391. Org Lett. 2006. PMID: 16562867

7

Enantioselective direct aldol reactions catalyzed by L-prolinamide derivatives.

Tang Z, Jiang F, Cui X, Gong LZ, Mi AQ, Jiang YZ, Wu YD. Tang Z, et al. Proc Natl Acad Sci U S A. 2004 Apr 20;101(16):5755-60. doi: 10.1073/pnas.0307176101. Epub 2004 Apr 12. Proc Natl Acad Sci U S A. 2004. PMID: 15079057 Free PMC article.

8

A highly efficient organocatalyst for direct aldol reactions of ketones with aldehydes [corrected].

Tang Z, Yang ZH, Chen XH, Cun LF, Mi AQ, Jiang YZ, Gong LZ. Tang Z, et al. J Am Chem Soc. 2005 Jun 29;127(25):9285-9. doi: 10.1021/ja0510156. J Am Chem Soc. 2005. PMID: 15969611

9

Novel small organic molecules for a highly enantioselective direct aldol reaction.

Tang Z, Jiang F, Yu LT, Cui X, Gong LZ, Mi AQ, Jiang YZ, Wu YD. Tang Z, et al. J Am Chem Soc. 2003 May 7;125(18):5262-3. doi: 10.1021/ja034528q. J Am Chem Soc. 2003. PMID: 12720423

10

Small peptides catalyze highly enantioselective direct aldol reactions of aldehydes with hydroxyacetone: unprecedented regiocontrol in aqueous media.

Tang Z, Yang ZH, Cun LF, Gong LZ, Mi AQ, Jiang YZ. Tang Z, et al. Org Lett. 2004 Jun 24;6(13):2285-7. doi: 10.1021/ol049141m. Org Lett. 2004. PMID: 15200341

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