1414964-50-3Relevant academic research and scientific papers
Facile access to 2,5-disubstituted-4-chloromethyl-3-iodofuran derivatives via ICl-mediated cyclization of 1-alkyl-2-alkynylallylic alcohols
Thongsornkleeb, Charnsak,Rabten, Wangchuk,Ruchirawat, Somsak,Bunrit, Anon,Tummatorn, Jumreang
supporting information, p. 6615 - 6619,5 (2012/12/11)
Substituted furans are conveniently synthesized from acyclic secondary 1-alkyl-2-alkynylallylic alcohol precursors via an ICl-promoted cyclization reaction. The furans generated by this method incorporate both iodine and chlorine atoms which may be useful for further elaborations via many known methods. The methodology is suitable for generating a wide array of furan products which can serve as useful building blocks for the synthesis of various biologically active molecules.
Facile access to 2,5-disubstituted-4-chloromethyl-3-iodofuran derivatives via ICl-mediated cyclization of 1-alkyl-2-alkynylallylic alcohols
Thongsornkleeb, Charnsak,Rabten, Wangchuk,Bunrit, Anon,Tummatorn, Jumreang,Ruchirawat, Somsak
supporting information, p. 6615 - 6619 (2013/01/15)
Substituted furans are conveniently synthesized from acyclic secondary 1-alkyl-2-alkynylallylic alcohol precursors via an ICl-promoted cyclization reaction. The furans generated by this method incorporate both iodine and chlorine atoms which may be useful for further elaborations via many known methods. The methodology is suitable for generating a wide array of furan products which can serve as useful building blocks for the synthesis of various biologically active molecules.
