Zhang J - Search Results

1

Divergent access to N-hydroxypyrroles and isoxazoles via the gold(i)- or Brønsted acid-catalysed regioselective cyclization of N-(2-trifluoromethyl-3-alkynyl) oximes.

Zeng Q, Zhang L, Xiao Y, Zhang J. Zeng Q, et al. Among authors: zhang l, zhang j. Org Biomol Chem. 2018 Feb 21;16(8):1375-1380. doi: 10.1039/c7ob03107f. Org Biomol Chem. 2018. PMID: 29411001

2

Tetrasubstituted furans by a Pd(II)-catalyzed three-component Michael addition/cyclization/cross-coupling reaction.

Xiao Y, Zhang J. Xiao Y, et al. Among authors: zhang j. Angew Chem Int Ed Engl. 2008;47(10):1903-6. doi: 10.1002/anie.200704531. Angew Chem Int Ed Engl. 2008. PMID: 18232034 No abstract available.

3

Efficient assembly of allenes, 1,3-dienes, and 4H-pyrans by catalytic regioselective nucleophilic addition to electron-deficient 1,3-conjugated enynes.

Yu X, Ren H, Xiao Y, Zhang J. Yu X, et al. Among authors: zhang j. Chemistry. 2008;14(28):8481-5. doi: 10.1002/chem.200801004. Chemistry. 2008. PMID: 18688833 No abstract available.

4

Rh(I)-catalyzed regio- and stereospecific carbonylation of 1-(1-alkynyl)cyclopropyl ketones: a modular entry to highly substituted 5,6-dihydrocyclopenta[c]furan-4-ones.

Zhang Y, Chen Z, Xiao Y, Zhang J. Zhang Y, et al. Among authors: zhang j. Chemistry. 2009;15(21):5208-11. doi: 10.1002/chem.200900413. Chemistry. 2009. PMID: 19360828

5

Furans versus 4H-pyrans: catalyst-controlled regiodivergent tandem Michael addition-cyclization reaction of 2-(1-alkynyl)-2-alken-1-ones with 1,3-dicarbonyl compounds.

Xiao Y, Zhang J. Xiao Y, et al. Among authors: zhang j. Chem Commun (Camb). 2009 Jun 28;(24):3594-6. doi: 10.1039/b905267d. Epub 2009 May 11. Chem Commun (Camb). 2009. PMID: 19521619

6

Tetrasubstituted allenes by Pd0-catalyzed three-component tandem Michael addition/cross-coupling reaction.

Xiao Y, Zhang J. Xiao Y, et al. Among authors: zhang j. Chem Commun (Camb). 2010 Feb 7;46(5):752-4. doi: 10.1039/b919060k. Epub 2009 Nov 27. Chem Commun (Camb). 2010. PMID: 20087509

7

Organocatalytic hetero [4+2] cycloaddition reactions of 2-(1-alkynyl)-2-alkene-1-ones: metal-free access to highly substituted 4H-pyrans.

Yu X, Cao Z, Zhang J. Yu X, et al. Among authors: zhang j. Org Biomol Chem. 2010 Nov 21;8(22):5059-61. doi: 10.1039/c0ob00334d. Epub 2010 Sep 27. Org Biomol Chem. 2010. PMID: 20871909

8

Gold(i)-catalyzed cyclization of 2-(1-alkynyl)-alk-2-en-1-one oximes: a facile access to highly substituted N-alkoxypyrroles.

Zhang M, Zhang J. Zhang M, et al. Among authors: zhang j. Chem Commun (Camb). 2012 May 22. doi: 10.1039/c2cc32510a. Online ahead of print. Chem Commun (Camb). 2012. PMID: 22617939

9

Pyrroles versus cyclic nitrones: catalyst-controlled divergent cyclization of N-(2-perfluoroalkyl-3-alkynyl) hydroxylamines.

Zeng Q, Zhang L, Yang J, Xu B, Xiao Y, Zhang J. Zeng Q, et al. Among authors: zhang l, zhang j. Chem Commun (Camb). 2014 Apr 25;50(32):4203-6. doi: 10.1039/c4cc00493k. Chem Commun (Camb). 2014. PMID: 24626793

10

Scandium-catalyzed tandem selective oxirane ring-opening/Friedel-Crafts alkylation: a facile access to [1,4]oxazino[4,3-a]indoles and 3,4-dihydro-1H-pyrrolo[2,1-c][1,4]oxazines.

Wei L, Liu L, Zhang J. Wei L, et al. Among authors: zhang j. Org Biomol Chem. 2014 Sep 21;12(35):6869-77. doi: 10.1039/c4ob01057d. Org Biomol Chem. 2014. PMID: 25053291

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