Carbohydrates to heterocycles: A new strategy for the synthesis of enantiomerically pure pyridazines and oxazines derived from epoxypyranoside scaffolds

Raed A. Al-Qawasmeh; Taleb H. Al-Tel; Raid J. Abdel-Jalil; Wolfgang Voelter

doi:10.1246/cl.1999.541

Carbohydrates to heterocycles: A new strategy for the synthesis of enantiomerically pure pyridazines and oxazines derived from epoxypyranoside scaffolds

Raed A. Al-Qawasmeh, Taleb H. Al-Tel, Raid J. Abdel-Jalil, Wolfgang Voelter

Chemistry

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

14 Citations (Scopus)

Abstract

An easy and high yield access to enantiomerically pure pyridazines and oxazines from epoxy pyranosides via ß-keto ester functionalization is described.

Original language	English
Pages (from-to)	541-542
Number of pages	2
Journal	Chemistry Letters
Issue number	7
DOIs	https://doi.org/10.1246/cl.1999.541
Publication status	Published - 1999

ASJC Scopus subject areas

General Chemistry

Access to Document

10.1246/cl.1999.541

Cite this

@article{6db9c29764844be999d0e9e6651bab16,

title = "Carbohydrates to heterocycles: A new strategy for the synthesis of enantiomerically pure pyridazines and oxazines derived from epoxypyranoside scaffolds",

abstract = "An easy and high yield access to enantiomerically pure pyridazines and oxazines from epoxy pyranosides via {\ss}-keto ester functionalization is described.",

author = "Al-Qawasmeh, {Raed A.} and Al-Tel, {Taleb H.} and Abdel-Jalil, {Raid J.} and Wolfgang Voelter",

year = "1999",

doi = "10.1246/cl.1999.541",

language = "English",

pages = "541--542",

journal = "Chemistry Letters",

issn = "0366-7022",

publisher = "Chemical Society of Japan",

number = "7",

}

TY - JOUR

T1 - Carbohydrates to heterocycles

T2 - A new strategy for the synthesis of enantiomerically pure pyridazines and oxazines derived from epoxypyranoside scaffolds

AU - Al-Qawasmeh, Raed A.

AU - Al-Tel, Taleb H.

AU - Abdel-Jalil, Raid J.

AU - Voelter, Wolfgang

PY - 1999

Y1 - 1999

N2 - An easy and high yield access to enantiomerically pure pyridazines and oxazines from epoxy pyranosides via ß-keto ester functionalization is described.

AB - An easy and high yield access to enantiomerically pure pyridazines and oxazines from epoxy pyranosides via ß-keto ester functionalization is described.

UR - http://www.scopus.com/inward/record.url?scp=0033473992&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0033473992&partnerID=8YFLogxK

U2 - 10.1246/cl.1999.541

DO - 10.1246/cl.1999.541

M3 - Article

AN - SCOPUS:0033473992

SN - 0366-7022

SP - 541

EP - 542

JO - Chemistry Letters

JF - Chemistry Letters

IS - 7

ER -

Carbohydrates to heterocycles: A new strategy for the synthesis of enantiomerically pure pyridazines and oxazines derived from epoxypyranoside scaffolds

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this