Tetrahedron Letters

Cyclopropanone equivalents. Formation of 1-pyrrolizidione by a dicyclopropyl imine rearrangement.

HH Wasserman, RP Dion

Index: Wasserman, Harry H.; Dion, Robert P. Tetrahedron Letters, 1982 , vol. 23, # 13 p. 1413 - 1416

Full Text: HTML

Citation Number: 26

Abstract

Download full text in PDF Opens in a new window. Article suggestions will be shown in a dialog on return to ScienceDirect. ... Please enable JavaScript to use all the features on this page. ... Cyclopropanone equivalents. Formation of 1-pyrrolizidione by a dicyclopropyl imine rearrangement. ... A dicyclopropyl ketimine may be formed by the addition of cyclopropyllithium to 1-cyano-1-piperidinocyclopropane. Rearrangement of the ketimine takes place under ...

~49%

Intramolecular azide-diene cycloadditions. An approach to fu...

[Pearson, William H.; Celebuski, Joseph E.; Poon, Yam-Foo; Dixon, Brian R.; Glans, Jeffrey H. Tetrahedron Letters, 1986 , vol. 27, # 52 p. 6301 - 6304]

Synthesis of (±)-isoretronecanol,(±)-curassanecine,(±)-helio...

[Tetrahedron Letters, , vol. 43, # 43 p. 7725 - 7728]

Synthesis of (-)-slaframine and related indolizidines

[Journal of Organic Chemistry, , vol. 57, # 14 p. 3977 - 3987]

Cyclopropanone equivalents from 3-chloropropionic acid. Use ...

[Tetrahedron, , vol. 45, # 10 p. 3203 - 3216]