Palladium(II)-catalysed intramolecular oxypalladation/functionalisation of carbohydrate-derived cyclic alkenes. Regioselective formation of substituted di- and tetra-hydropyrans

Cedric W. Holzapfel; Lizel Marais

doi:10.1039/a807768a

Palladium(II)-catalysed intramolecular oxypalladation/functionalisation of carbohydrate-derived cyclic alkenes. Regioselective formation of substituted di- and tetra-hydropyrans

Cedric W. Holzapfel, Lizel Marais

Chemical Sciences

University of Johannesburg

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

3 Citations (Scopus)

Abstract

A palladium(II)-promoted domino process converts easily prepared pseudoglycals into highly functionalised, chiral di- and tetra-hydropyran structures in high yields.

Original language	English
Pages (from-to)	190-191
Number of pages	2
Journal	Journal of Chemical Research - Part S
Issue number	3
DOIs	https://doi.org/10.1039/a807768a
Publication status	Published - Mar 1999

ASJC Scopus subject areas

General Chemistry

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title = "Palladium(II)-catalysed intramolecular oxypalladation/functionalisation of carbohydrate-derived cyclic alkenes. Regioselective formation of substituted di- and tetra-hydropyrans",

abstract = "A palladium(II)-promoted domino process converts easily prepared pseudoglycals into highly functionalised, chiral di- and tetra-hydropyran structures in high yields.",

author = "Holzapfel, {Cedric W.} and Lizel Marais",

year = "1999",

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journal = "Journal of Chemical Research - Part S",

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AU - Marais, Lizel

PY - 1999/3

Y1 - 1999/3

N2 - A palladium(II)-promoted domino process converts easily prepared pseudoglycals into highly functionalised, chiral di- and tetra-hydropyran structures in high yields.

AB - A palladium(II)-promoted domino process converts easily prepared pseudoglycals into highly functionalised, chiral di- and tetra-hydropyran structures in high yields.

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DO - 10.1039/a807768a

M3 - Article

AN - SCOPUS:0033038426

SN - 0308-2342

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JO - Journal of Chemical Research - Part S

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Palladium(II)-catalysed intramolecular oxypalladation/functionalisation of carbohydrate-derived cyclic alkenes. Regioselective formation of substituted di- and tetra-hydropyrans

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