Abstract
Evidence obtained by carbon labelling and carbene-scavenging techniques for the establishment of an α-oxocarbene-oxirene interconversion in the photolysis of acyclic α-diazoketones is summarised. Normalsized alicyclic α-diazoketones and o-quinone diazides react without intervention of the oxirene route, whereas the 12-membered ring system behaves like the acyclic counterparts. The oxirene participation is discussed with reference to stereochemical features of the α-diazoketones and predictions derived from high-level theory.
Keywords: diazo carbonyl compounds, 13c-labelling, oxirenes, oxocarbenes, photochemistry, rearrangement mechanisms
Related Books
Advances in Organic Synthesis
The Synthetic Methods, Structures, and Properties of the Ca-C σ Bond Organocalcium Containing Compounds
Advances in Organic Synthesis
Chemistry of Bipyrazoles: Synthesis and Applications
Advances in Organic Synthesis
Advanced Nanocatalysis for Organic Synthesis and Electroanalysis
Advances in Organic Synthesis
Advances in Organic Synthesis
3