134 related articles for article (PubMed ID: 15471470)
1. Temperature-controlled regioselectivity in the reductive cleavage of p-methoxybenzylidene acetals.
Hernández-Torres JM; Achkar J; Wei A
J Org Chem; 2004 Oct; 69(21):7206-11. PubMed ID: 15471470
[TBL] [Abstract][Full Text] [Related]
2. 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; 342(3-4):627-30. PubMed ID: 17118348
[TBL] [Abstract][Full Text] [Related]
3. Experimental observations on the reductive cleavage of endo and exo 3,4-O-benzylidene fucopyranoside derivatives.
Studzian M; Pérez ME; Arias-Pérez MS
Carbohydr Res; 2021 Jul; 505():108338. PubMed ID: 34023694
[TBL] [Abstract][Full Text] [Related]
4. 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; 69(25):8694-701. PubMed ID: 15575745
[TBL] [Abstract][Full Text] [Related]
5. 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; 338(8):697-703. PubMed ID: 12668088
[TBL] [Abstract][Full Text] [Related]
6. Systematic Study of Regioselective Reductive Ring-Opening Reactions of 4,6-
Mezö E; Herczeg M; Demeter F; Bereczki I; Csávás M; Borbás A
J Org Chem; 2021 Sep; 86(18):12973-12987. PubMed ID: 34478619
[TBL] [Abstract][Full Text] [Related]
7. Regioselective Reductive Opening of Benzylidene Acetals with Dichlorophenylborane/Triethylsilane: Previously Unreported Side Reactions and How to Prevent Them.
Hénault J; Quellier P; Mock-Joubert M; Le Narvor C; Alix A; Bonnaffé D
J Org Chem; 2022 Jan; 87(2):963-973. PubMed ID: 35015527
[TBL] [Abstract][Full Text] [Related]
8. 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; 346(12):1633-7. PubMed ID: 21601182
[TBL] [Abstract][Full Text] [Related]
9. 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; 343(17):2997-3000. PubMed ID: 18789434
[TBL] [Abstract][Full Text] [Related]
10. 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; 391():93-6. PubMed ID: 24792317
[TBL] [Abstract][Full Text] [Related]
11. Regioselective reductive openings of 4,6-benzylidene acetals: synthetic and mechanistic aspects.
Ohlin M; Johnsson R; Ellervik U
Carbohydr Res; 2011 Sep; 346(12):1358-70. PubMed ID: 21531396
[TBL] [Abstract][Full Text] [Related]
12. Reductive opening of carbohydrate phenylsulfonylethylidene (PSE) acetals.
Chéry F; Cabianca E; Tatibouët A; De Lucchi O; Lindhorst TK; Rollin P
Carbohydr Res; 2015 Nov; 417():117-24. PubMed ID: 26469209
[TBL] [Abstract][Full Text] [Related]
13. 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; 44(11):1665-8. PubMed ID: 15685675
[No Abstract] [Full Text] [Related]
14. 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; 9(22):7655-8. PubMed ID: 21922112
[TBL] [Abstract][Full Text] [Related]
15. 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; 345(18):2709-13. PubMed ID: 21055729
[TBL] [Abstract][Full Text] [Related]
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; 1(8):1330-41. PubMed ID: 12929663
[TBL] [Abstract][Full Text] [Related]
17. Desymmetrization of trehalose via regioselective DIBAL reductive ring opening of benzylidene and substituted benzylidene acetals.
Sarpe VA; Kulkarni SS
Org Biomol Chem; 2013 Oct; 11(38):6460-5. PubMed ID: 23982734
[TBL] [Abstract][Full Text] [Related]
18. 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; 346(7):927-32. PubMed ID: 21440246
[TBL] [Abstract][Full Text] [Related]
19. Regioselective reductive cleavage of bis-benzylidene acetal: stereoselective synthesis of anticancer agent OGT2378 and glycosidase inhibitor 1,4-dideoxy-1,4-imino-l-xylitol.
Aravind A; Sankar MG; Varghese B; Baskaran S
J Org Chem; 2009 Apr; 74(7):2858-61. PubMed ID: 19278232
[TBL] [Abstract][Full Text] [Related]
20. Cyanuric chloride/sodium borohydride: a new reagent combination for reductive opening of 4,6-benzylidene acetals of carbohydrates to primary alcohols.
Tatina M; Yousuf SK; Aravinda S; Singh B; Mukherjee D
Carbohydr Res; 2013 Nov; 381():142-5. PubMed ID: 24103734
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
