Ultrasonic energy promoted allylation to generate 1-C-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)prop-2-ene

Mark Farrell; Ciaran O’Reilly; Dilip V. Jarikote; Paul V. Murphy; Jani Rahkila

doi:10.1201/b16602

Ultrasonic energy promoted allylation to generate 1-C-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)prop-2-ene

Mark Farrell, Ciaran O’Reilly, Dilip V. Jarikote, Paul V. Murphy, Jani Rahkila

Infectious Disease

Research output: Chapter in Book or Conference Publication/Proceeding › Chapter › peer-review

Abstract

In recent years C-glycoside formation has been of interest. It has been established that C-glycoside analogues of naturally occurring O-glycosides can often display interesting differences in their reactivity and biological activity. The synthesis of many different C-glycosyl compounds commences from a glycosyl prop-2-ene.

Original language	English
Title of host publication	Carbohydrate Chemistry
Subtitle of host publication	Proven Synthetic Methods
Publisher	CRC Press
Pages	33-37
Number of pages	5
Volume	2
ISBN (Electronic)	9781439875957
ISBN (Print)	9781439875940
DOIs	https://doi.org/10.1201/b16602
Publication status	Published - 1 Jan 2014

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abstract = "In recent years C-glycoside formation has been of interest. It has been established that C-glycoside analogues of naturally occurring O-glycosides can often display interesting differences in their reactivity and biological activity. The synthesis of many different C-glycosyl compounds commences from a glycosyl prop-2-ene.",

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AU - Jarikote, Dilip V.

AU - Murphy, Paul V.

AU - Rahkila, Jani

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AB - In recent years C-glycoside formation has been of interest. It has been established that C-glycoside analogues of naturally occurring O-glycosides can often display interesting differences in their reactivity and biological activity. The synthesis of many different C-glycosyl compounds commences from a glycosyl prop-2-ene.

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Ultrasonic energy promoted allylation to generate 1-C-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)prop-2-ene

Abstract

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