Ab initio study of Diels-Alder reactions of cyclopentadiene with ethylene, isoprene, cyclopentadiene, acrylonitrile, and methyl vinyl ketone

1993 ◽  
Vol 115 (7) ◽  
pp. 2936-2942 ◽  
Author(s):  
William L. Jorgensen ◽  
Dongchul Lim ◽  
James F. Blake
Keyword(s):  
Ab Initio ◽  
Diels Alder ◽  
Vinyl Ketone ◽  
Methyl Vinyl Ketone ◽  
Ab Initio Study ◽  
Methyl Vinyl

scholarly journals The Diels-Alder reaction of 3-acetoxy-1-vinylcyclohexene with methyl vinyl ketone.

1989 ◽  
Vol 37 (9) ◽  
pp. 2307-2309 ◽  
Author(s):  
Takeshi KAWAMATA ◽  
Kenzo HARIMAYA ◽  
Yoichi IITAKA ◽  
Seiichi INAYAMA
Keyword(s):  
Alder Reaction ◽  
Diels Alder ◽  
Vinyl Ketone ◽  
Methyl Vinyl Ketone ◽  
Methyl Vinyl ◽  
Diels Alder Reaction

Diels–Alder cycloadditions of vinyl- and propenyl-allene to methyl vinyl ketone

1968 ◽  
Vol 0 (19) ◽  
pp. 1141-1142 ◽  
Author(s):  
M. Bertrand ◽  
J. Grimaldi ◽  
B. Waegell
Keyword(s):  
Diels Alder ◽  
Vinyl Ketone ◽  
Methyl Vinyl Ketone ◽  
Methyl Vinyl

scholarly journals Attempted Diels-Alder Reactions on Vindoline Derivatives

2017 ◽  
Vol 61 (4) ◽  
pp. 258 ◽  
Author(s):  
Szabolcs Mayer ◽  
Péter Keglevich ◽  
Péter Ábrányi-Balogh ◽  
Áron Szigetvári ◽  
Miklós Dékány ◽  
...  
Keyword(s):  
Alder Reaction ◽  
Diels Alder ◽  
Vinyl Ketone ◽  
Methyl Vinyl Ketone ◽  
Methyl Vinyl ◽  
Diels Alder Reaction ◽  
Quinone Derivative

The Diels-Alder reaction of vindoline and methyl vinyl ketone resulted in a Friedel-Crafts reaction product. In the reaction between the ortho-quinone derivative of vindoline and N-phenylmaleimide, two anomalous products were obtained, a vindoline dimer, and a condensed vindoline derivative.

Rearrangements in the Diterpenoid Series. I. The Solvolysis of Methyl 15β-tosyloxy-13-isopropyl-17-noratis-13-en-18-oate

1973 ◽  
Vol 51 (1) ◽  
pp. 77-86 ◽  
Author(s):  
William A. Ayer ◽  
Pandurang D. Deshpande
Keyword(s):  
Diels Alder ◽  
Vinyl Ketone ◽  
Methyl Vinyl Ketone ◽  
Unsaturated Ketone ◽  
Methyl Vinyl ◽  
Levopimaric Acid ◽  
Alder Adduct

The synthesis of methyl 15β-hydroxy-13-isopropyl-17-noratis-13-en-18-oate (14b) is described. Compound 14b was prepared from the ketone 12b, in turn derived from the Diels–Alder adduct formed between levopimaric acid (7) and α-acetoxyacrylonitrile. Solvolysis of the tosylate of 14b proceeds predominantly with rearrangement and elimination to give methyl 16-isopropylidene-7,17-secoacon-8(15)-en-18-oate (16a). This rearrangement serves as a model for the proposed biosynthetic transformation of atisine-type alkaloids into alkaloids of the aconitine series. The degradation of 16a into the unsaturated ketone 19, which contains the 19 carbons of the aconane skeleton, is described. The Diels–Alder addition of methyl vinyl ketone to levopimaric acid is reported and the adduct is shown to possess structure 8.

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