Epoxy pyranoses, chiral synthons for versatile regio- and stereocontrolled functionalizations

W. Voelter; R. Thürmer; R. A. Al-Qawasmeh; T. H. Al-Tel; R. Abdel-Jalil; Y. Al-Abed

Epoxy pyranoses, chiral synthons for versatile regio- and stereocontrolled functionalizations

W. Voelter^*, R. Thürmer, R. A. Al-Qawasmeh, T. H. Al-Tel, R. Abdel-Jalil, Y. Al-Abed

^*Corresponding author for this work

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

3 Citations (Scopus)

Abstract

From epoxy sugars, neighbouring an O-triflyl residue, efficient short-cut new routes to aminodeoxy, (amino acid)-deoxy, cyclopropanated, β-hydroxyketo or γ-butyrolactone pyranoses are developed.

Original language	English
Pages (from-to)	55-69
Number of pages	15
Journal	Polish Journal of Chemistry
Volume	73
Issue number	1
Publication status	Published - 1999
Externally published	Yes

Keywords

(amino acid)-deoxy sugars
Aminodeoxy sugars
Canadensolide
Cyclopropanated sugars
Epoxy pyranoses
Triflate pyranoses
β-hydroxyketo sugars

ASJC Scopus subject areas

General Chemistry

Cite this

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title = "Epoxy pyranoses, chiral synthons for versatile regio- and stereocontrolled functionalizations",

abstract = "From epoxy sugars, neighbouring an O-triflyl residue, efficient short-cut new routes to aminodeoxy, (amino acid)-deoxy, cyclopropanated, β-hydroxyketo or γ-butyrolactone pyranoses are developed.",

keywords = "(amino acid)-deoxy sugars, Aminodeoxy sugars, Canadensolide, Cyclopropanated sugars, Epoxy pyranoses, Triflate pyranoses, β-hydroxyketo sugars",

author = "W. Voelter and R. Th{\"u}rmer and Al-Qawasmeh, {R. A.} and Al-Tel, {T. H.} and R. Abdel-Jalil and Y. Al-Abed",

year = "1999",

language = "English",

volume = "73",

pages = "55--69",

journal = "Polish Journal of Chemistry",

issn = "0137-5083",

publisher = "Polish Chemical Society",

number = "1",

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TY - JOUR

T1 - Epoxy pyranoses, chiral synthons for versatile regio- and stereocontrolled functionalizations

AU - Voelter, W.

AU - Thürmer, R.

AU - Al-Qawasmeh, R. A.

AU - Al-Tel, T. H.

AU - Abdel-Jalil, R.

AU - Al-Abed, Y.

PY - 1999

Y1 - 1999

N2 - From epoxy sugars, neighbouring an O-triflyl residue, efficient short-cut new routes to aminodeoxy, (amino acid)-deoxy, cyclopropanated, β-hydroxyketo or γ-butyrolactone pyranoses are developed.

AB - From epoxy sugars, neighbouring an O-triflyl residue, efficient short-cut new routes to aminodeoxy, (amino acid)-deoxy, cyclopropanated, β-hydroxyketo or γ-butyrolactone pyranoses are developed.

KW - (amino acid)-deoxy sugars

KW - Aminodeoxy sugars

KW - Canadensolide

KW - Cyclopropanated sugars

KW - Epoxy pyranoses

KW - Triflate pyranoses

KW - β-hydroxyketo sugars

UR - http://www.scopus.com/inward/record.url?scp=0033475040&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0033475040&partnerID=8YFLogxK

M3 - Article

AN - SCOPUS:0033475040

SN - 0137-5083

VL - 73

SP - 55

EP - 69

JO - Polish Journal of Chemistry

JF - Polish Journal of Chemistry

IS - 1

ER -

Epoxy pyranoses, chiral synthons for versatile regio- and stereocontrolled functionalizations

Abstract

Keywords

ASJC Scopus subject areas

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