Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 297

1.

The presence of water improves reductive openings of benzylidene acetals with trimethylaminoborane and aluminium chloride.

Sherman AA, Mironov YV, Yudina ON, Nifantiev NE.

Carbohydr Res. 2003 Apr 4;338(8):697-703.

PMID:
12668088
2.

Some observations on the reductive ring opening of 4,6-O-benzylidene acetals of hexopyranosides with the borane trimethylamine-aluminium chloride reagent.

Daragics K, Szabó P, Fügedi P.

Carbohydr Res. 2011 Sep 6;346(12):1633-7. doi: 10.1016/j.carres.2011.04.046. Epub 2011 May 3.

PMID:
21601182
3.

Reductive openings of benzylidene acetals. Kinetic studies of borane and alane activation by Lewis acids.

Johnsson R, Cukalevski R, Dragén F, Ivanisevic D, Johansson I, Petersson L, Wettergren EE, Yam KB, Yang B, Ellervik U.

Carbohydr Res. 2008 Nov 24;343(17):2997-3000. doi: 10.1016/j.carres.2008.08.022. Epub 2008 Aug 29.

PMID:
18789434
4.

Regioselective reductive openings of 4,6-benzylidene acetals: synthetic and mechanistic aspects.

Ohlin M, Johnsson R, Ellervik U.

Carbohydr Res. 2011 Sep 6;346(12):1358-70. doi: 10.1016/j.carres.2011.03.032. Epub 2011 Apr 1. Review.

PMID:
21531396
5.

Regioselective ring opening of exo- and endo-3,4-benzylidene acetals of arabinopyranoside derivatives with Lewis acids and reducing agents.

Rujirawanich J, Kongkathip B, Kongkathip N.

Carbohydr Res. 2011 May 15;346(7):927-32. doi: 10.1016/j.carres.2011.01.031. Epub 2011 Mar 6.

PMID:
21440246
6.

Deuterium-isotope study on the reductive ring opening of benzylidene acetals.

Lee IC, Zulueta MM, Shie CR, Arco SD, Hung SC.

Org Biomol Chem. 2011 Oct 26;9(22):7655-8. doi: 10.1039/c1ob06056b. Epub 2011 Sep 16.

PMID:
21922112
7.

Use of methanesulfonic acid in the reductive ring-opening of O-benzylidene acetals.

Zinin AI, Malysheva NN, Shpirt AM, Torgov VI, Kononov LO.

Carbohydr Res. 2007 Feb 26;342(3-4):627-30. Epub 2006 Oct 13.

PMID:
17118348
8.

HClO4-silica-catalysed regioselective opening of benzylidene acetals and its application towards regioselective HO-4 glycosylation of benzylidene acetals in one-pot.

Dara S, Saikam V, Yadav M, Singh PP, Vishwakarma RA.

Carbohydr Res. 2014 Jun 4;391:93-6. doi: 10.1016/j.carres.2014.01.011. Epub 2014 Feb 11.

PMID:
24792317
9.

Regioselective ring opening of benzylidene acetal protecting group(s) of hexopyranoside derivatives by DIBAL-H.

Tanaka N, Ogawa I, Yoshigase S, Nokami J.

Carbohydr Res. 2008 Oct 13;343(15):2675-9. doi: 10.1016/j.carres.2008.07.017. Epub 2008 Aug 3.

PMID:
18718576
10.

A total synthesis of hydroxylysine in protected form and investigations of the reductive opening of p-methoxybenzylidene acetals.

Gustafsson T, Schou M, Almqvist F, Kihlberg J.

J Org Chem. 2004 Dec 10;69(25):8694-701.

PMID:
15575745
11.

Iodine-sodium cyanoborohydride-mediated reductive ring opening of 4,6-O-benzylidene acetals of hexopyranosides.

Rao KV, Patil PR, Atmakuri S, Kartha KP.

Carbohydr Res. 2010 Dec 10;345(18):2709-13. doi: 10.1016/j.carres.2010.10.013. Epub 2010 Oct 20.

PMID:
21055729
12.
14.

Cu(OTf)2 as an efficient and dual-purpose catalyst in the regioselective reductive ring opening of benzylidene acetals.

Shie CR, Tzeng ZH, Kulkarni SS, Uang BJ, Hsu CY, Hung SC.

Angew Chem Int Ed Engl. 2005 Mar 4;44(11):1665-8. No abstract available.

PMID:
15685675
15.
16.

Deoxygenation of carbohydrates by thiol-catalysed radical-chain redox rearrangement of the derived benzylidene acetals.

Dang HS, Roberts BP, Sekhon J, Smits TM.

Org Biomol Chem. 2003 Apr 21;1(8):1330-41.

PMID:
12929663
17.

Stereoselective (2-naphthyl)methylation of sugar hydroxyls by the hydrogenolysis of diastereoisomeric dioxolane-type (2-naphthyl)methylene acetals.

Borbás A, Szabó ZB, Szilágyi L, Bényei A, Lipták A.

Carbohydr Res. 2002 Nov 19;337(21-23):1941-51.

PMID:
12433460
18.

Temperature-controlled regioselectivity in the reductive cleavage of p-methoxybenzylidene acetals.

Hernández-Torres JM, Achkar J, Wei A.

J Org Chem. 2004 Oct 15;69(21):7206-11.

20.

Reductive opening of carbohydrate phenylsulfonylethylidene (PSE) acetals.

Chéry F, Cabianca E, Tatibouët A, De Lucchi O, Lindhorst TK, Rollin P.

Carbohydr Res. 2015 Nov 19;417:117-24. doi: 10.1016/j.carres.2015.09.011. Epub 2015 Sep 26.

PMID:
26469209

Supplemental Content

Support Center