95455-17-7Relevant academic research and scientific papers
INTRAMOLECULAR REACTIONS OF-PROPYNYLSILANES WITH N-ACYLIMINIUM; CUPRATES SN2' REACTIONS OF THE ALLENIC PRODUCTS AS A ROUTE TO TRANS-FUSED CARBOBICYCLES
Klaver, Wim J.,Moolenaar, Marinus J.,Hiemstra, Henk,Speckamp, W. Nico
, p. 3805 - 3818 (2007/10/02)
Intramolecular acid-assisted reactions of 2-propynylsilanes with cyclic N-acyliminium ion precursors lead to bridged azabicyclic systems 34-45 (Table I), containing the uncommon α-allenic amide funcionality.After introduction of a tert-butoxycarbonyl or a
SILICON-ASSISTED SYNTHESIS OF BRIDGED AZABICYCLIC SYSTEMS VIA N-ACILIMINIUM INTERMEDIATES
Klaver, Wim J.,Hiemstra, Henk,Speckamp, W. Nico
, p. 6729 - 6738 (2007/10/02)
Intramolecular acid-mediated reactions of 2-propynyl- and allylsilanes with five- and six-membered cyclic N-acyliminium ion precursors lead to bridged azabicyclic compounds (Table I).Neat formic acid is the reaction medium of choice in most cases.The cycl
NOVEL APPROACH TO TRANS-FUSED CARBOBICYCLES
Hiemstra, Henk,Klaver, Wim J.,Moolenaar, Marinus J.,Speckamp, W. Nico
, p. 5453 - 5456 (2007/10/02)
The combination of a silicon directed N-acyliminium ion cyclization reaction and a subsequent SN2' substitution of an imide nitrogen with lithium dimethyl cuprate constitutes a novel approach to funcionalized trans-fused carbobicycles.
