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A One-Step Procedure for the Monoacylation of Symmetrical 1,2-Diols

โœ Scribed by Clarke, Paul A.; Kayaleh, Nadim E.; Smith, Martin A.; Baker, James R.; Bird, Stephan J.; Chan, Chuen

Book ID
120834610
Publisher
American Chemical Society
Year
2002
Tongue
English
Weight
91 KB
Volume
67
Category
Article
ISSN
0022-3263

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๐Ÿ“œ SIMILAR VOLUMES

A One-Step Procedure for the Monoacylati
A One-Step Procedure for the Monoacylation of Symmetrical 1,2-Diols.
โœ Paul A. Clarke; Nadim E. Kayaleh; Martin A. Smith; James R. Baker; Stephan J. Bi ๐Ÿ“‚ Article ๐Ÿ“… 2003 ๐Ÿ› John Wiley and Sons โš– 212 KB ๐Ÿ‘ 3 views

## Abstract For Abstract see ChemInform Abstract in Full Text.

Direct one step mono-functionalisation o
Direct one step mono-functionalisation of symmetrical 1,2-diols
โœ Paul A Clarke; Robert A Holton; Nadim E Kayaleh ๐Ÿ“‚ Article ๐Ÿ“… 2000 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 123 KB

The mono-functionalisation of meso-and C 2 -symmetric diols has been achieved via the use of a new lanthanide(III) chloride catalysed acylation reaction.

A mild procedure for the conversion of 1
A mild procedure for the conversion of 1,2-diols to olefins
โœ E.J. Corey; B. Hopkins ๐Ÿ“‚ Article ๐Ÿ“… 1982 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 238 KB

An improved procedure for the stereospecific synthesis of olefhm from 1,2-dials via the corresponding thionocarbonate is described. The introduction of the versatile oleflnic function by &oxygenation of a 1,2-diol is a useful technique in organic synthesis. Although numerous procedures have appeare