82980-12-9Relevant articles and documents
Versus Cycloadditions with 1-Ethoxyethene and Heterocyclic Aldehydes; Formation of Vinyl Compounds
Merour, Jean-Yves,Bourlot, Anne-Sophie,Desarbre, Eric
, p. 3527 - 3530 (1995)
Inverse electron demand Diels-Alder reactions of ethoxyethene with heterocyclic aldehydes afforded a mixture of cycloadducts and vinyl compounds resulting from a competing pathway.
Synthesis of vinylindoles and vinylpyrroles by the Peterson olefination or by use of the Nysted reagent
Noland, Wayland E.,Etienne, Christopher L.,Lanzatella, Nicholas P.
experimental part, p. 381 - 388 (2011/05/14)
Vinylindoles and vinylpyrroles were prepared from their corresponding aldehydes or ketones using the Peterson olefination, or by use of the Nysted reagent, a commercially available gem-dimetallic compound. The two methods provide efficient and convenient
Efficient one-pot synthesis of anti HIV and antitumor compounds: Harman and substituted harmans
Kusurkar, Radhika S.,Goswami, Shailesh K.,Vyas, Sandhya M.
, p. 4761 - 4763 (2007/10/03)
Anti HIV and antitumor compounds, harman and substituted harmans have been synthesized using electrocyclization reactions as key steps. A one-pot reaction sequence was used to furnish these compounds in good overall yield.
