The intramolecular acylation of some hex-, hept-, and oct-enoic acids
作者:M. F. Ansell、J. C. Emmett、R. V. Coombs
DOI:10.1039/j39680000217
日期:——
acids. Intramolecular acylation of these acids in the presence of trifluoroacetic anhydride is shown to be dependent on the structure and stereochemistry of the acids. The formation of cyclohept-2-enone from hept-6-enoic acid is reported. Concentrated sulphuric acid in acetic anhydride is shown to convert hex- and hept-5-enoic acid into phenyl and o-tolyl acetate, respectively. Some improved syntheses
Synth�se d'alcools ac�tyl�niques par alkylation d'hydroxy-?-alkynes-1
作者:Jacques Flahaut、Philippe Miginiac
DOI:10.1002/hlca.19780610635
日期:1978.9.20
Synthesis of acetylenic alcohols by alkylation of ω‐hydroxy‐1‐alkynesIn liquid ammonia and with lithium amide, the alkylation of an ω‐hydroxyl‐alkyne proceeds with good yield with primary or secondary alcohols and with fair yield with tertiary alcohols. It is a very convenient way to prepare many substituted acetylenic alcohols.