Combination of NH2OH·HCl and NaIO4: an effective reagent for molecular iodine-free regioselective 1,2-difunctionalization of olefins and easy access of terminal acetals
A new metal-free protocol is described for the synthesis of terminal acetals by tandem oxidative rearrangement of olefins using oxone as an oxidant in the presence of iodine. Moreover, a one-pot procedure for the preparation of glycol mono esters from olefins is also presented for the first time using the same reagent system.
Combination of NH<sub>2</sub>OH·HCl and NaIO<sub>4</sub>: an effective reagent for molecular iodine-free regioselective 1,2-difunctionalization of olefins and easy access of terminal acetals
作者:Nirnita Chakraborty、Sougata Santra、Shrishnu Kumar Kundu、Alakananda Hajra、Grigory V. Zyryanov、Adinath Majee
DOI:10.1039/c5ra11092k
日期:——
We have demonstrated a new application of our oxidizing reagent, a combination of NH2OH·HCl and NaIO4, in the first generalized regioselective 1,2-difunctionalization of olefins.