Investigation of the H-bond-mediated aglycone delivery reaction in application to the synthesis of β-glucosides

Michael P. Mannino; Jagodige P. Yasomanee; Alexei V. Demchenko

doi:10.1016/j.carres.2018.09.003

Investigation of the H-bond-mediated aglycone delivery reaction in application to the synthesis of β-glucosides

Michael P. Mannino, Jagodige P. Yasomanee, Alexei V. Demchenko

University of Missouri-St. Louis

Research output: Contribution to journal › Article › peer-review

Original language	American English
Journal	Carbohydrate Research
Volume	470
DOIs	https://doi.org/10.1016/j.carres.2018.09.003
State	Published - Dec 1 2018

Disciplines

Biology
Organic Chemistry
Biochemistry

Access to Document

10.1016/j.carres.2018.09.003License: Unspecified

Cite this

@article{9d8a90fb0f604cbd940923615bb09884,

title = "Investigation of the H-bond-mediated aglycone delivery reaction in application to the synthesis of β-glucosides",

author = "Mannino, \{Michael P.\} and Yasomanee, \{Jagodige P.\} and Demchenko, \{Alexei V.\}",

note = "JavaScript is disabled on your browser. Please enable JavaScript to use all the features on this page. * The HAD-capable glycosyl donor showed a great variation of the results depending on the nature of acceptors used. * Primary acceptors, both carbohydrate and aliphatic alcohols afforded the glycosylation products with complete β-selectivity.",

year = "2018",

month = dec,

day = "1",

doi = "10.1016/j.carres.2018.09.003",

language = "American English",

volume = "470",

journal = "Carbohydrate Research",

}

TY - JOUR

T1 - Investigation of the H-bond-mediated aglycone delivery reaction in application to the synthesis of β-glucosides

AU - Mannino, Michael P.

AU - Yasomanee, Jagodige P.

AU - Demchenko, Alexei V.

N1 - JavaScript is disabled on your browser. Please enable JavaScript to use all the features on this page. * The HAD-capable glycosyl donor showed a great variation of the results depending on the nature of acceptors used. * Primary acceptors, both carbohydrate and aliphatic alcohols afforded the glycosylation products with complete β-selectivity.

PY - 2018/12/1

Y1 - 2018/12/1

UR - https://www.sciencedirect.com/science/article/pii/S0008621518304890

U2 - 10.1016/j.carres.2018.09.003

DO - 10.1016/j.carres.2018.09.003

M3 - Article

VL - 470

JO - Carbohydrate Research

JF - Carbohydrate Research

ER -

Investigation of the H-bond-mediated aglycone delivery reaction in application to the synthesis of β-glucosides

Disciplines

Access to Document

Other files and links

Cite this