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Items: 1 to 20 of 87

1.

A novel base-induced isomerization gives access to unprecedented (E)-exo-glycals.

Eppe G, Dumitrescu L, Pierrot O, Li T, Pan W, Vincent SP.

Chemistry. 2013 Aug 26;19(35):11547-52. doi: 10.1002/chem.201300969.

PMID:
23893767
2.

Synthesis of Unprecedented Sulfonylated Phosphono-exo-Glycals Designed as Inhibitors of the Three Mycobacterial Galactofuranose Processing Enzymes.

Frédéric CJ, Tikad A, Fu J, Pan W, Zheng RB, Koizumi A, Xue X, Lowary TL, Vincent SP.

Chemistry. 2016 Oct 24;22(44):15913-15920. doi: 10.1002/chem.201603161.

PMID:
27628709
3.

Stereochemistry in the synthesis and reaction of exo-glycals.

Yang WB, Yang YY, Gu YF, Wang SH, Chang CC, Lin CH.

J Org Chem. 2002 May 31;67(11):3773-82.

PMID:
12027693
4.

Enantioselective synthesis of tertiary α-hydroxy phosphonates catalyzed by carbohydrate/cinchona alkaloid thiourea organocatalysts.

Kong S, Fan W, Wu G, Miao Z.

Angew Chem Int Ed Engl. 2012 Aug 27;51(35):8864-7. doi: 10.1002/anie.201204287. No abstract available. Erratum in: Angew Chem Int Ed Engl. 2012 Oct 1;51(40):9960.

PMID:
22847899
5.

Copper-catalyzed synthesis of α-hydroxy phosphonates from H-phosphonates and alcohols or ethers.

Zhao Z, Xue W, Gao Y, Tang G, Zhao Y.

Chem Asian J. 2013 Apr;8(4):713-6. doi: 10.1002/asia.201201062. No abstract available.

PMID:
23345018
6.

Palladium catalyzed stereoselective C-glycosylation of glycals with enol triflates.

Bai Y, Leow M, Zeng J, Liu XW.

Org Lett. 2011 Oct 21;13(20):5648-51. doi: 10.1021/ol202368n.

PMID:
21954934
7.

A general method for convergent synthesis of functionalized exo-glycals based on halogenation and Suzuki cross-coupling of 1-exo-methylene sugars.

Gómez AM, Danelón GO, Pedregosa A, Valverde S, López JC.

Chem Commun (Camb). 2002 Sep 21;(18):2024-5.

PMID:
12357761
8.
9.

Carbohydrate-2-deoxy-2-phosphonates: simple synthesis and Horner-Emmons reaction.

Elamparuthi E, Linker T.

Angew Chem Int Ed Engl. 2009;48(10):1853-5. doi: 10.1002/anie.200804725.

PMID:
19170148
10.

Ready access to 3-amino-2,3-dideoxysugars via regio- and stereo-selective tandem hydroamination-glycosylation of glycals.

Ding F, William R, Wang S, Gorityala BK, Liu XW.

Org Biomol Chem. 2011 May 21;9(10):3929-39. doi: 10.1039/c1ob05068k.

PMID:
21451824
12.

Stereospecific debenzylative cycloetherification of carbohydrate-derived allylic alcohols, ethers and esters to form vinyl C-furanosides.

Cribiù R, Cumpstey I.

Chem Commun (Camb). 2008 Mar 14;(10):1246-8. doi: 10.1039/b718060h.

PMID:
18309432
13.

Montmorillonite K-10 clay-catalyzed Ferrier rearrangement of 2-C-hydroxymethyl-d-glycals, 3,4,6-tri-O-alkyl-d-glycals, and 3,4-(dihydro-2H-pyran-5-yl)methanol: a few unexpected domino transformations.

Kumaran E, Santhi M, Balasubramanian KK, Bhagavathy S.

Carbohydr Res. 2011 Sep 27;346(13):1654-61. doi: 10.1016/j.carres.2011.03.027.

PMID:
21696711
14.

Subtle stereochemical and electronic effects in iridium-catalyzed isomerization of C-allyl glycosides.

Patnam R, Juarez-Ruiz JM, Roy R.

Org Lett. 2006 Jun 22;8(13):2691-4.

PMID:
16774233
15.

Convenient syntheses and transformations of 2-C-malonyl carbohydrates.

Yin J, Sommermann T, Linker T.

Chemistry. 2007;13(36):10152-67.

PMID:
17955558
16.

One-pot synthesis of 1-exo-alkylidene-2,3-anhydro furanoses: convenient precursors for exo-glycals and functionalized C-glycals.

Gómez AM, Pedregosa A, Valverde S, López JC.

Chem Commun (Camb). 2002 Sep 21;(18):2022-3.

PMID:
12357760
17.

Development of the scope of a co-mediated O-->C rearrangement reaction.

Meek SJ, Pradaux F, Carbery DR, Demont EH, Harrity JP.

J Org Chem. 2005 Nov 25;70(24):10046-56.

PMID:
16292838
18.

Conversion of D-glucals into L-glycals and mirror-image carbohydrates.

Boulineau FP, Wei A.

Org Lett. 2004 Jan 8;6(1):119-21.

PMID:
14703365
19.
20.

Tandem RCM-isomerization approach to glycals of desoxyheptoses from a common precursor.

Schmidt B, Biernat A.

Org Lett. 2008 Jan 3;10(1):105-8.

PMID:
18067307
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