An aqueous medium-controlled stereospecific oxidative iodination of alkynes: efficient access to (E)-diiodoalkene derivatives

New J. Chem., 2018, Advance Article DOI: 10.1039/C8NJ03929A, LetterRammurthy Banothu, Swamy Peraka, Srujana Kodumuri, Durgaiah Chevella, Krishna Sai Gajula, Vasu Amrutham, Divya Rohini Yennamaneni, Narender Nama A new and versatile approach for the stereospecific iodination of alkynes has been developed in aqueous media. Scale-up reactions (up to 5 g) established the proficiency of this protocol and highlight the feasibility of large scale reactions. To cite this article before page numbers are assigned, use the DOI form of citation above. The content of this RSS Feed (c) The Royal Society of Chemistry

Source: RSC - New J. Chem. latest articles - October 16, 2018 Category: Chemistry Authors: Rammurthy Banothu Source Type: research