141 related articles for article (PubMed ID: 22509217)
1. Electrochemical generation of 2,3-oxazolidinone glycosyl triflates as an intermediate for stereoselective glycosylation.
Nokami T; Shibuya A; Saigusa Y; Manabe S; Ito Y; Yoshida J
Beilstein J Org Chem; 2012; 8():456-60. PubMed ID: 22509217
[TBL] [Abstract][Full Text] [Related]
2. Taming the Reactivity of Glycosyl Iodides To Achieve Stereoselective Glycosidation.
Gervay-Hague J
Acc Chem Res; 2016 Jan; 49(1):35-47. PubMed ID: 26524481
[TBL] [Abstract][Full Text] [Related]
3. Alpha- and beta-glycosyl sulfonium ions: generation and reactivity.
Nokami T; Shibuya A; Manabe S; Ito Y; Yoshida J
Chemistry; 2009; 15(10):2252-5. PubMed ID: 19156648
[TBL] [Abstract][Full Text] [Related]
4. Are Brønsted Acids the True Promoter of Metal-Triflate-Catalyzed Glycosylations? A Mechanistic Probe into 1,2-
Sletten ET; Tu YJ; Schlegel HB; Nguyen HM
ACS Catal; 2019 Mar; 9(3):2110-2123. PubMed ID: 31819822
[TBL] [Abstract][Full Text] [Related]
5. Electrochemical generation of glycosyl triflate pools.
Nokami T; Shibuya A; Tsuyama H; Suga S; Bowers AA; Crich D; Yoshida J
J Am Chem Soc; 2007 Sep; 129(35):10922-8. PubMed ID: 17696345
[TBL] [Abstract][Full Text] [Related]
6. Glycosylation from the non-reducing end using a combination of thioglycoside and glycosyl sulfoxide as the glycosyl donor and the acceptor.
Kajimoto T; Arimitsu K; Ozeki M; Node M
Chem Pharm Bull (Tokyo); 2010 May; 58(5):758-64. PubMed ID: 20460812
[TBL] [Abstract][Full Text] [Related]
7. Stereodirecting Effect of C5-Carboxylate Substituents on the Glycosylation Stereochemistry of 3-Deoxy-d- manno-oct-2-ulosonic Acid (Kdo) Thioglycoside Donors: Stereoselective Synthesis of α- and β-Kdo Glycosides.
Huang W; Zhou YY; Pan XL; Zhou XY; Lei JC; Liu DM; Chu Y; Yang JS
J Am Chem Soc; 2018 Mar; 140(10):3574-3582. PubMed ID: 29481074
[TBL] [Abstract][Full Text] [Related]
8. Additive-controlled stereoselective glycosylations of 2,3-oxazolidinone protected glucosamine or galactosamine thioglycoside donors with phenols based on preactivation protocol.
Qin Q; Xiong DC; Ye XS
Carbohydr Res; 2015 Feb; 403():104-14. PubMed ID: 25108483
[TBL] [Abstract][Full Text] [Related]
9. Evaluation of thioglycosides of Kdo as glycosyl donors.
Mannerstedt K; Ekelöf K; Oscarson S
Carbohydr Res; 2007 Feb; 342(3-4):631-7. PubMed ID: 17027943
[TBL] [Abstract][Full Text] [Related]
10. Stereoselective 1,2-cis glycosylation of 2-O-allyl protected thioglycosides.
Aloui M; Chambers DJ; Cumpstey I; Fairbanks AJ; Redgrave AJ; Seward CM
Chemistry; 2002 Jun; 8(11):2608-21. PubMed ID: 12180341
[TBL] [Abstract][Full Text] [Related]
11. 1-Benzenesulfinyl piperidine/trifluoromethanesulfonic anhydride: a potent combination of shelf-stable reagents for the low-temperature conversion of thioglycosides to glycosyl triflates and for the formation of diverse glycosidic linkages.
Crich D; Smith M
J Am Chem Soc; 2001 Sep; 123(37):9015-20. PubMed ID: 11552809
[TBL] [Abstract][Full Text] [Related]
12. N,N-Diacetylsialyl chloride--a novel readily accessible sialyl donor in reactions with neutral and charged nucleophiles in the absence of a promoter.
Orlova AV; Shpirt AM; Kulikova NY; Kononov LO
Carbohydr Res; 2010 Apr; 345(6):721-30. PubMed ID: 20149348
[TBL] [Abstract][Full Text] [Related]
13. S-(4-methoxyphenyl) benzenethiosulfinate (MPBT)/trifluoromethanesulfonic anhydride: a convenient system for the generation of glycosyl triflates from thioglycosides.
Crich D; Smith M
Org Lett; 2000 Dec; 2(25):4067-9. PubMed ID: 11112645
[TBL] [Abstract][Full Text] [Related]
14. S-Benzoxazolyl (SBox) glycosides as novel, versatile glycosyl donors for stereoselective 1,2-cis glycosylation.
Demchenko AV; Malysheva NN; De Meo C
Org Lett; 2003 Feb; 5(4):455-8. PubMed ID: 12583742
[TBL] [Abstract][Full Text] [Related]
15. Direct chemical glycosylation with pentenyl- and thioglycoside donors of N-acetylglucosamine.
Krag J; Christiansen MS; Petersen JG; Jensen HH
Carbohydr Res; 2010 May; 345(7):872-9. PubMed ID: 20304386
[TBL] [Abstract][Full Text] [Related]
16. Dissecting the Essential Role of Anomeric β-Triflates in Glycosylation Reactions.
Santana AG; Montalvillo-Jiménez L; Díaz-Casado L; Corzana F; Merino P; Cañada FJ; Jiménez-Osés G; Jiménez-Barbero J; Gómez AM; Asensio JL
J Am Chem Soc; 2020 Jul; 142(28):12501-12514. PubMed ID: 32579343
[TBL] [Abstract][Full Text] [Related]
17. Synthesis of a 2-N,N-dibenzylamino glucopyranosyl trichloroacetimidate glycosyl donor and evaluation of its utility in stereoselective glycosylation.
Ali SP; Jalsa NK
Carbohydr Res; 2016 Feb; 420():13-22. PubMed ID: 26717545
[TBL] [Abstract][Full Text] [Related]
18. DIDMH in combination with triflic acid - A new promoter system for thioglycoside glycosyl donors.
Heuckendorff M; Jensen HH
Carbohydr Res; 2018 Jan; 455():86-91. PubMed ID: 29175659
[TBL] [Abstract][Full Text] [Related]
19. Remote Activation of Disarmed Thioglycosides in Latent-Active Glycosylation via Interrupted Pummerer Reaction.
Xiao X; Zhao Y; Shu P; Zhao X; Liu Y; Sun J; Zhang Q; Zeng J; Wan Q
J Am Chem Soc; 2016 Oct; 138(40):13402-13407. PubMed ID: 27617339
[TBL] [Abstract][Full Text] [Related]
20. α-Selective Glycosylation with β-Glycosyl Sulfonium Ions Prepared via Intramolecular Alkylation.
Moons SJ; Mensink RA; Bruekers JPJ; Vercammen MLA; Jansen LM; Boltje TJ
J Org Chem; 2019 Apr; 84(7):4486-4500. PubMed ID: 30808170
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
