C6 picoloyl protection: A remote stereodirecting group for 2-deoxy-β-glycoside formation

Jyh Herng Ruei; Patteti Venukumar; Arun B. Ingle; Kwok-Kong Mong

doi:10.1039/c4cc08465a

C6 picoloyl protection: A remote stereodirecting group for 2-deoxy-β-glycoside formation

Jyh Herng Ruei, Patteti Venukumar, Arun B. Ingle, Kwok-Kong Mong^*

^*Corresponding author for this work

Department of Applied Chemistry

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

39 Scopus citations

Abstract

We reported a remote control glycosylation method using the picoloyl protecting group for 2-deoxy-β-glycosidic bond formation. The method is applicable to various 2-deoxythioglycosyl donors and the utility is illustrated by the synthesis of a deoxytrisaccharide component of landomycins. This journal is

Original language	English
Pages (from-to)	5394-5397
Number of pages	4
Journal	Chemical Communications
Volume	51
Issue number	25
DOIs	https://doi.org/10.1039/c4cc08465a
State	Published - 28 Mar 2015

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title = "C6 picoloyl protection: A remote stereodirecting group for 2-deoxy-β-glycoside formation",

abstract = "We reported a remote control glycosylation method using the picoloyl protecting group for 2-deoxy-β-glycosidic bond formation. The method is applicable to various 2-deoxythioglycosyl donors and the utility is illustrated by the synthesis of a deoxytrisaccharide component of landomycins. This journal is",

author = "Ruei, {Jyh Herng} and Patteti Venukumar and Ingle, {Arun B.} and Kwok-Kong Mong",

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T2 - A remote stereodirecting group for 2-deoxy-β-glycoside formation

AU - Ruei, Jyh Herng

AU - Venukumar, Patteti

AU - Ingle, Arun B.

AU - Mong, Kwok-Kong

PY - 2015/3/28

Y1 - 2015/3/28

N2 - We reported a remote control glycosylation method using the picoloyl protecting group for 2-deoxy-β-glycosidic bond formation. The method is applicable to various 2-deoxythioglycosyl donors and the utility is illustrated by the synthesis of a deoxytrisaccharide component of landomycins. This journal is

AB - We reported a remote control glycosylation method using the picoloyl protecting group for 2-deoxy-β-glycosidic bond formation. The method is applicable to various 2-deoxythioglycosyl donors and the utility is illustrated by the synthesis of a deoxytrisaccharide component of landomycins. This journal is

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U2 - 10.1039/c4cc08465a

DO - 10.1039/c4cc08465a

M3 - Article

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AN - SCOPUS:84925047404

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EP - 5397

JO - Chemical Communications

JF - Chemical Communications

SN - 1359-7345

IS - 25

ER -

C6 picoloyl protection: A remote stereodirecting group for 2-deoxy-β-glycoside formation

Abstract

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