
TY  - JOUR
A1  - Buckland, SJ 
A1  - Halton, B 
A1  - Mei, Q 
A1  - Stang, PJ 
T1  - Studies in the Cycloproparene Series: Reactions of Alkylidenecycloproparenes With Electrophiles
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1987
VL  - 40
IS  - 8
SP  - 1375
EP  - 1387
KW  - 
UR  - https://doi.org/10.1071/CH9871375 
N2  - The addition of an electrophile to the alkylidenecycloproparenes (2a-d) is dominated by capture at the exocyclic centre with formation of the corresponding cycloproparenyl cation, e.g. (15). Subsequent reaction with the counter ion is usually accompanied by cleavage of the three-membered ring. Thus compounds (2) give the ethanones (4) with aqueous acids whilst anhydrous acetic acid yields the vinyl acetates (5). Silver(1)-catalysed methanolysis of (2) leads to vinyl ethers (6); the alkyne (7) is formed only from (2d) which carries a vinylic proton. Brominations and bromine water additions lead to products of ring expansion (8)-(10) or ring cleavage (11)-(14) depending upon the conditions employed. These latter reactions demonstrate a delicate balance between cycloproparenylcarbinyl cation formation and cleavage of the three-membered ring. 
ER  -

