Fleet GWJ - Search Results

1

Synthesis and Glycosidase Inhibition of Broussonetine M and Its Analogues.

Wu QK, Kinami K, Kato A, Li YX, Fleet GWJ, Yu CY, Jia YM. Wu QK, et al. Among authors: fleet gwj. Molecules. 2019 Oct 15;24(20):3712. doi: 10.3390/molecules24203712. Molecules. 2019. PMID: 31619020 Free PMC article.

2

Nitrogen-containing furanose and pyranose analogues from Hyacinthus orientalis.

Asano N, Kato A, Miyauchi M, Kizu H, Kameda Y, Watson AA, Nash RJ, Fleet GW. Asano N, et al. J Nat Prod. 1998 May;61(5):625-8. doi: 10.1021/np9705726. J Nat Prod. 1998. PMID: 9599261

3

Homonojirimycin isomers and N-alkylated homonojirimycins: structural and conformational basis of inhibition of glycosidases.

Asano N, Nishida M, Kato A, Kizu H, Matsui K, Shimada Y, Itoh T, Baba M, Watson AA, Nash RJ, Lilley PM, Watkin DJ, Fleet GW. Asano N, et al. J Med Chem. 1998 Jul 2;41(14):2565-71. doi: 10.1021/jm970836l. J Med Chem. 1998. PMID: 9651160

4

Polyhydroxylated pyrrolidine and pyrrolizidine alkaloids from Hyancinthoides non-scripta and Scilla campanulata.

Kato A, Adachi I, Miyauchi M, Ikeda K, Komae T, Kizu H, Kameda Y, Watson AA, Nash RJ, Wormald MR, Fleet GW, Asano N. Kato A, et al. Carbohydr Res. 1999 Mar 31;316(1-4):95-103. doi: 10.1016/s0008-6215(99)00043-9. Carbohydr Res. 1999. PMID: 10515698

5

Novel alpha-L-fucosidase inhibitors from the bark of Angylocalyx pynaertii (Leguminosae).

Asano N, Yasuda K, Kizu H, Kato A, Fan JQ, Nash RJ, Fleet GW, Molyneux RJ. Asano N, et al. Eur J Biochem. 2001 Jan;268(1):35-41. doi: 10.1046/j.1432-1327.2001.01837.x. Eur J Biochem. 2001. PMID: 11121099 Free article.

6

New sugar-mimic alkaloids from the pods of Angylocalyx pynaertii.

Yasuda K, Kizu H, Yamashita T, Kameda Y, Kato A, Nash RJ, Fleet GW, Molyneux RJ, Asano N. Yasuda K, et al. J Nat Prod. 2002 Feb;65(2):198-202. doi: 10.1021/np010360f. J Nat Prod. 2002. PMID: 11858756

7

Ring-chain tautomerism in organic synthesis: synthesis of heterocyclic enamines from a novel and practical formal ring transformation reaction of lactones.

Wang MX, Liu Y, Gao HY, Zhang Y, Yu CY, Huang ZT, Fleet GW. Wang MX, et al. J Org Chem. 2003 Apr 18;68(8):3281-6. doi: 10.1021/jo026560t. J Org Chem. 2003. PMID: 12688802

8

A direct retro-Reformatsky fragmentation: formal ring enlargement of cyclic ketones for novel and practical synthesis of heterocyclic enamines.

Zhao MX, Wang MX, Yu CY, Huang ZT, Fleet GW. Zhao MX, et al. J Org Chem. 2004 Feb 6;69(3):997-1000. doi: 10.1021/jo0351320. J Org Chem. 2004. PMID: 14750839

9

Looking glass inhibitors: L-DMDP, a more potent and specific inhibitor of alpha-glucosidases than the enantiomeric natural product DMDP.

Yu CY, Asano N, Ikeda K, Wang MX, Butters TD, Wormald MR, Dwek RA, Winters AL, Nash RJ, Fleet GW. Yu CY, et al. Chem Commun (Camb). 2004 Sep 7;(17):1936-7. doi: 10.1039/b406035k. Epub 2004 Jul 29. Chem Commun (Camb). 2004. PMID: 15340609

10

Isolation of glycosidase-inhibiting hyacinthacines and related alkaloids from Scilla socialis.

Kato A, Kato N, Adachi I, Hollinshead J, Fleet GW, Kuriyama C, Ikeda K, Asano N, Nash RJ. Kato A, et al. J Nat Prod. 2007 Jun;70(6):993-7. doi: 10.1021/np0700826. Epub 2007 May 31. J Nat Prod. 2007. PMID: 17536859

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