37 / 2023-08-09 14:40:43
Diformyloxylation of Unactivated Alkenes with Formic Acid
Diformyloxylation; Unactivated alkenes; Formic acid
Abstract Accepted
Junchen Li / State Key Laboratory of NBC Protection for Civilian
Xiaojing Bi / State Key Laboratory of NBC Protection for Civilian
Alkene dioxygenation serve as a straightforward and powerful transformation for the preparation of 1,2-diol skeletons which are widely exiting in pharmaceuticals and bioactive natural products. Versatile strategies have been developed to modulate such reaction, including Prévost-Woodward reaction, Sharpless reaction, metal-participated or metal-free dioxygenations. We disclosed a novel and efficient diformyloxylation of allylphosphorates with the employment of DIH as the mediator and formic acid as the formyloxylating reagent. Good functionality compatibility was achieved and homoallyl phosphoric compounds could also participated in the diformyloxylation with good yields. Whereas, other types of carboxylic acids gave the iodoesterification mixtures under same conditions, and other types of allylic alkenes showed inert reactivity. Reaction monitoring and radical inhibition experiments revealed that the diformyloxylation might proceed with a DIH-mediated ionic iodoformyloxylation process, followed by a DIH-mediated radical process which might involve a intramolecular H-bonding between C-I bond and acyl hydrogen of the iodoformyloxylation products (Figure 1).
Important Date
  • Conference Date

    Nov 12

    2023

    to

    Nov 16

    2023

  • Oct 24 2023

    Draft paper submission deadline

  • Nov 16 2023

    Registration deadline

Sponsored By
Ningbo University
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