181 related articles for article (PubMed ID: 28228850)
21. Is an acyl group at O-3 in glucosyl donors able to control α-stereoselectivity of glycosylation? The role of conformational mobility and the protecting group at O-6.
Komarova BS; Orekhova MV; Tsvetkov YE; Nifantiev NE
Carbohydr Res; 2014 Jan; 384():70-86. PubMed ID: 24368161
[TBL] [Abstract][Full Text] [Related]
22. Mapping the Relationship between Glycosyl Acceptor Reactivity and Glycosylation Stereoselectivity.
van der Vorm S; van Hengst JMA; Bakker M; Overkleeft HS; van der Marel GA; Codée JDC
Angew Chem Int Ed Engl; 2018 Jul; 57(27):8240-8244. PubMed ID: 29603532
[TBL] [Abstract][Full Text] [Related]
23. Glycosyl Exchange of Unactivated Glycosidic Bonds: Suppressing or Embracing Side Reactivity in Catalytic Glycosylations.
Martin JL; Sati GC; Malakar T; Hatt J; Zimmerman PM; Montgomery J
J Org Chem; 2022 May; 87(9):5817-5826. PubMed ID: 35413188
[TBL] [Abstract][Full Text] [Related]
24. Stereoselective protecting-group-free synthesis of alkyl glycosides using dibenzyloxy triazine type glycosyl donors.
Li G; Noguchi M; Ishihara M; Takagi Y; Nagaki M; Saito S; Saito M; Ye XS; Shoda SI
Carbohydr Res; 2023 Dec; 534():108940. PubMed ID: 37738819
[TBL] [Abstract][Full Text] [Related]
25. A Ring Contraction of 2,3-Di- O-Silylated Thiopyranosides To Give Thiofuranosides under Mildly Acidic Conditions.
Abronina PI; Malysheva NN; Litvinenko VV; Zinin AI; Kolotyrkina NG; Kononov LO
Org Lett; 2018 Oct; 20(19):6051-6054. PubMed ID: 30216074
[TBL] [Abstract][Full Text] [Related]
26. Glycosylation with 2-Acetamido-2-deoxyglycosyl Donors at a Low Temperature: Scope of the Non-Oxazoline Method.
Arihara R; Kakita K; Suzuki N; Nakamura S; Hashimoto S
J Org Chem; 2015 May; 80(9):4259-77. PubMed ID: 25807142
[TBL] [Abstract][Full Text] [Related]
27. Remote Electronic Effects by Ether Protecting Groups Fine-Tune Glycosyl Donor Reactivity.
Heuckendorff M; Poulsen LT; Jensen HH
J Org Chem; 2016 Jun; 81(12):4988-5006. PubMed ID: 27224456
[TBL] [Abstract][Full Text] [Related]
28. Regioselective silylation of N-phthaloylchitosan with TBDMS and TBDPS groups.
Binette A; Gagnon J
Biomacromolecules; 2007 Jun; 8(6):1812-5. PubMed ID: 17487971
[TBL] [Abstract][Full Text] [Related]
29. Advances in Protecting Groups for Oligosaccharide Synthesis.
Ghosh B; Kulkarni SS
Chem Asian J; 2020 Feb; 15(4):450-462. PubMed ID: 31895493
[TBL] [Abstract][Full Text] [Related]
30. 1,3-syn-Diaxial Repulsion of Typical Protecting Groups Used in Carbohydrate Chemistry in 3-O-Substituted Derivatives of Isopropyl d-Idopyranosides.
Komarova BS; Gerbst AG; Finogenova AM; Dmitrenok AS; Tsvetkov YE; Nifantiev NE
J Org Chem; 2017 Sep; 82(17):8897-8908. PubMed ID: 28748699
[TBL] [Abstract][Full Text] [Related]
31. Synthesis of silylene and silyl(silylene)metal complexes.
Ogino H
Chem Rec; 2002; 2(5):291-306. PubMed ID: 12369054
[TBL] [Abstract][Full Text] [Related]
32. Self-promoted and stereospecific formation of
Nielsen MM; Mała P; Baldursson EÞ; Pedersen CM
Chem Sci; 2019 May; 10(20):5299-5307. PubMed ID: 31191886
[TBL] [Abstract][Full Text] [Related]
33. SilE-R and SilE-S-DABB Proteins Catalying Enantiospecific Hydrolysis of Organosilyl Ethers.
Pick LM; Oehme V; Hartmann J; Wenzlaff J; Tang Q; Grogan G; Ansorge-Schumacher MB
Angew Chem Int Ed Engl; 2024 Jun; 63(25):e202404105. PubMed ID: 38630059
[TBL] [Abstract][Full Text] [Related]
34. Comparison of glycosyl donors: a supramer approach.
Orlova AV; Malysheva NN; Panova MV; Podvalnyy NM; Medvedev MG; Kononov LO
Beilstein J Org Chem; 2024; 20():181-192. PubMed ID: 38318458
[TBL] [Abstract][Full Text] [Related]
35. Gold(I)-Catalyzed Glycosylation with Glycosyl o-Alkynylbenzoates as Donors.
Yu B
Acc Chem Res; 2018 Feb; 51(2):507-516. PubMed ID: 29297680
[TBL] [Abstract][Full Text] [Related]
36. Bromine-Promoted Glycosidation of Conformationally Superarmed Thioglycosides.
Panza M; Civera M; Yasomanee JP; Belvisi L; Demchenko AV
Chemistry; 2019 Sep; 25(51):11831-11836. PubMed ID: 31286579
[TBL] [Abstract][Full Text] [Related]
37. Reactivity, Selectivity, and Synthesis of 4-C-Silylated Glycosyl Donors and 4-Deoxy Analogues.
Jaeger Pedersen M; Pedersen CM
Angew Chem Int Ed Engl; 2021 Feb; 60(5):2689-2693. PubMed ID: 33025650
[TBL] [Abstract][Full Text] [Related]
38. Regioselective silyl/acetate exchange of disaccharides yields advanced glycosyl donor and acceptor precursors.
Hsieh HW; Schombs MW; Witschi MA; Gervay-Hague J
J Org Chem; 2013 Oct; 78(19):9677-88. PubMed ID: 23980653
[TBL] [Abstract][Full Text] [Related]
39. Design of chemical glycosyl donors: does changing ring conformation influence selectivity/reactivity?
Satoh H; Manabe S
Chem Soc Rev; 2013 May; 42(10):4297-309. PubMed ID: 23364773
[TBL] [Abstract][Full Text] [Related]
40. Mapping the effect of configuration and protecting group pattern on glycosyl acceptor reactivity.
van Hengst JMA; Hellemons RJC; Remmerswaal WA; van de Vrande KNA; Hansen T; van der Vorm S; Overkleeft HS; van der Marel GA; Codée JDC
Chem Sci; 2023 Feb; 14(6):1532-1542. PubMed ID: 36794180
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
