Mechanistic insight into benzylidene-directed glycosylation reactions using cryogenic infrared spectroscopy
The stereoselective formation of 1,2-cis glycosidic linkages is challenging. The currently most widely used strategy for their installation uses 4,6-O-benzylidene-protected building blocks. The stereoselectivity of this reaction is thought to be driven by a covalent intermediate, which reacts via an...
Autori principali: | Chang, C, Greis, K, Prabhu, GRD, Wehner, D, Kirschbaum, C, Ober, K, Torres-Boy, AY, Leichnitz, S, Meijer, G, von Helden, G, Seeberger, PH, Pagel, K |
---|---|
Natura: | Journal article |
Lingua: | English |
Pubblicazione: |
Nature Research
2024
|
Documenti analoghi
Documenti analoghi
-
Unravelling the structural complexity of glycolipids with cryogenic infrared spectroscopy
di: Carla Kirschbaum, et al.
Pubblicazione: (2021-02-01) -
Unravelling the structure of glycosyl cations via cold-ion infrared spectroscopy
di: Eike Mucha, et al.
Pubblicazione: (2018-10-01) -
Publisher Correction: Unravelling the structure of glycosyl cations via cold-ion infrared spectroscopy
di: Eike Mucha, et al.
Pubblicazione: (2018-11-01) -
BENZYLIDENE ACETALS OF HEPTONOLACTONES
di: Bichard, C, et al.
Pubblicazione: (1993) -
Use of Detector Tubes in Analytical Chemistry
di: Leichnitz, K.
Pubblicazione: (1986-12-01)