Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 103

1.

Synthesis of a series of maltotriose phosphates with an evaluation of the utility of a fluorous phosphate protecting group.

Liu L, Pohl NL.

Carbohydr Res. 2013 Mar 22;369:14-24. doi: 10.1016/j.carres.2012.12.015. Epub 2012 Dec 24.

PMID:
23376679
2.

A fluorous phosphate protecting group with applications to carbohydrate synthesis.

Liu L, Pohl NL.

Org Lett. 2011 Apr 1;13(7):1824-7. doi: 10.1021/ol2003435. Epub 2011 Mar 8.

3.

Oligosaccharide synthesis with glycosyl phosphate and dithiophosphate triesters as glycosylating agents.

Plante OJ, Palmacci ER, Andrade RB, Seeberger PH.

J Am Chem Soc. 2001 Oct 3;123(39):9545-54.

PMID:
11572674
4.

Synthesis of phosphorylated 3,4-branched trisaccharides corresponding to LPS inner core structures of Neisseria meningitidis and Haemophilus influenzae.

Olsson JD, Oscarson S.

Carbohydr Res. 2010 Jul 2;345(10):1331-8. doi: 10.1016/j.carres.2010.03.006. Epub 2010 Mar 7.

PMID:
20347067
5.

Fluorous linker facilitated synthesis of teichoic acid fragments.

Hogendorf WF, Lameijer LN, Beenakker TJ, Overkleeft HS, Filippov DV, Codée JD, Van der Marel GA.

Org Lett. 2012 Feb 3;14(3):848-51. doi: 10.1021/ol2033652. Epub 2012 Jan 20.

PMID:
22264133
6.

Efficient regioselective chemical modifications of maltotriose: an easy access to oligosaccharidic scaffold.

Thiebault N, Lesur D, Godé P, Moreau V, Djedaïni-Pilard F.

Carbohydr Res. 2008 Nov 3;343(16):2719-28. doi: 10.1016/j.carres.2008.04.035. Epub 2008 May 7.

PMID:
18723165
7.

Froc: a new fluorous protective group for peptide and oligosaccharide synthesis.

Manzoni L, Castelli R.

Org Lett. 2006 Mar 2;8(5):955-7.

PMID:
16494483
9.

Fluorous Boc ((F)Boc) carbamates: new amine protecting groups for use in fluorous synthesis.

Luo Z, Williams J, Read RW, Curran DP.

J Org Chem. 2001 Jun 15;66(12):4261-6.

PMID:
11397162
10.

One-pot-synthesis of alpha-linked deoxy sugar trisaccharides.

Köpper S, Thiem J.

Carbohydr Res. 1994 Jul 16;260(2):219-32.

PMID:
8069874
11.

Protecting-group-free synthesis of glycosyl 1-phosphates.

Edgar LJ, Dasgupta S, Nitz M.

Org Lett. 2012 Aug 17;14(16):4226-9. doi: 10.1021/ol3019083. Epub 2012 Jul 30.

PMID:
22846058
12.

Synthetic studies on the trisaccharide intermediate of resin glycoside merremoside H(2).

Shen XQ, Xie L, Gao L, He LL, Yang Q, Yang JS.

Carbohydr Res. 2009 Oct 12;344(15):2063-8. doi: 10.1016/j.carres.2009.08.005. Epub 2009 Aug 11.

PMID:
19709649
13.

Stereoselective synthesis of P-modified α-glycosyl phosphates by the oxazaphospholidine approach.

Noro M, Fujita S, Wada T.

Org Lett. 2013 Dec 6;15(23):5948-51. doi: 10.1021/ol402785h. Epub 2013 Nov 13.

PMID:
24224562
14.

Synthesis of [6"-3H]-, (6"-2H)- and (2-2H)-maltotriose.

Sauerbrei B, Niggemann J, Gröger S, Lee S, Floss HG.

Carbohydr Res. 1996 Jan 11;280(2):223-35.

PMID:
8593637
16.

Synthesis of a di- and a trisaccharide related to the O-antigen of Escherichia coli O83:K24:H31.

Agnihotri G, Misra AK.

Carbohydr Res. 2006 Oct 16;341(14):2420-5. Epub 2006 Aug 1.

PMID:
16884704
17.

Strong competitive inhibition of porcine pancreatic alpha-amylase by aminodeoxy derivatives of maltose and maltotriose.

Lehmann J, Schmidt-Schuchardt M, Steck J.

Carbohydr Res. 1992 Dec 31;237:177-83.

PMID:
1294292
18.

Modified blood group A trisaccharide probes: synthesis and interaction with antibodies.

Shipova EV, Bovin NV.

Carbohydr Lett. 2001;4(2):85-90.

PMID:
11506162
19.

Rapid oligosaccharide synthesis using a fluorous protective group.

Miura T, Goto K, Waragai H, Matsumoto H, Hirose Y, Ohmae M, Ishida HK, Satoh A, Inazu T.

J Org Chem. 2004 Aug 6;69(16):5348-53.

PMID:
15287781
20.

Synthesis of a carboxyl linker containing Pk trisaccharide.

Hsieh SY, Jan MD, Patkar LN, Chen CT, Lin CC.

Carbohydr Res. 2005 Jan 17;340(1):49-57.

PMID:
15620666

Supplemental Content

Support Center