870010-48-3Relevant academic research and scientific papers
Enantioselective intramolecular cyclization of alkynyl esters catalyzed by a chiral Br?nsted base
Kondoh, Azusa,Tran, Hoa Thi Quynh,Kimura, Kyoko,Terada, Masahiro
supporting information, p. 5726 - 5729 (2016/05/19)
An enantioselective intramolecular cyclization reaction of alkynyl esters was developed, which employs a Br?nsted base catalyst generated in situ from a chiral Schiff base and t-BuOK. This reaction is a rare example of the enantioselective intramolecular addition of simple ester enolates to alkynes under Br?nsted base catalysis.
Pd-EnCat TPP30 as a catalyst for the generation of highly functionalized aryl- and alkenyl-substituted acetylenes via microwave-assisted sonogashira type reactions
Sedelmeier, Joerg,Ley, Steven V.,Lange, Heiko,Baxendale, Ian R.
supporting information; experimental part, p. 4412 - 4420 (2010/01/07)
We report a rapid microwave-assisted Sonogashira crosscoupling of aryl iodides and bromides with terminal alkynes using Pd-EnCat TPP30. Both electron-rich and electrondeficient aryl halides reacted smoothly with a broad variety of terminal alkynes in MeCN
Heterocycles by PtCl2-catalyzed intramolecular carboalkoxylation or carboamination of alkynes
Fuerstner, Alois,Davies, Paul W.
, p. 15024 - 15025 (2007/10/03)
PtCl2 constitutes a convenient catalyst for intramolecular hydroalkoxylation, carboalkoxylation, hydroamination, and carboamination reactions of alkynes, effecting the formation of substituted benzo[b]furan, indole-, and isochromene-1-one derivatives, respectively. This procedure allows for the transfer of (substituted) allyl, methoxymethyl (MOM), benzyloxymethyl (BOM), and (trimethylsilyl)ethoxymethyl (SEM) groups from oxygen to carbon and is compatible with functional groups that are susceptible to oxidative insertion of low valent metal species previously used for similar purposes. Although some of the reactions can even be carried out in air, the rates are significantly increased when conducted under an atmosphere of CO. A mechanistic rationale is proposed, implying activation of the alkyne by the carbophilic Pt(2+) template as the primary step of the catalytic cycle. Copyright
