Thermal rearrangement of allyl vinyl ether: heavy-atom kinetic isotope effects and the transition structure

L Kupczyk-Subotkowska, WH Saunders Jr…

Index: Kupczyk-Subotkowska, Lidia; Saunders Jr., William H.; Shine, Henry J.; Subotkowski, Witold Journal of the American Chemical Society, 1993 , vol. 115, # 14 p. 5957 - 5961

Full Text: HTML

Citation Number: 31

Abstract

Abstract: Kinetic isotope effects (KIE) in the rearrangement of allyl vinyl ether (1, 3-oxa-1, 5- hexadiene) to 4-pentenal (2) were measured for labeling with 14C at the 2-, 4-, and 6- positions and with 180 at the 3-position. BEBOVIB modeling calculations were applied successfully to the heavy-atom KIE and previously reported KIE for deuterium substitution at positions 4 and 6. From the calculations, it is deduced that the C4-0 bond is 50-70% ...

Related Articles:

2, 3-Dideoxy-DL-pentose

[Price,C.C.; Balsley,R.B. Journal of Organic Chemistry, 1966 , vol. 31, p. 3406 - 3407]

The mechanism of rearrangement of chorismic acid and related compounds

[Gajewski,J.J.; Jurayj,J.; Kimbrough,D.R. Journal of the American Chemical Society, 1987 , vol. 109, p. 1170]

Synthesis of allyl and alkyl vinyl ethers using an in situ prepared air-stable palladium catalyst. Efficient transfer vinylation of primary, secondary, and tertiary alcohols

[Bosch, Martin; Schlaf, Marcel Journal of Organic Chemistry, 2003 , vol. 68, # 13 p. 5225 - 5227]

Photochemistry of some carbonyl-conjugated 1, 5-hexadienes

[Crandall,J.K.; Mayer,C.F. Journal of Organic Chemistry, 1970 , vol. 35, # 9 p. 3049 - 3053]

Biomass conversion

[Paul et al. Bulletin de la Societe Chimique de France, 1950 , p. 121,126]

More Articles...