Liao_2020_J.Org.Chem_85_1298

Reference

Title : Increasing Structural Diversity of Natural Products by Michael Addition with ortho-Quinone Methide as the Acceptor - Liao_2020_J.Org.Chem_85_1298
Author(s) : Liao G , Fan J , Ludwig-Radtke L , Backhaus K , Li SM
Ref : J Org Chem , 85 :1298 , 2020
Abstract :

The active form of clavatol, ortho-quinone methide, can be generated from hydroxyclavatol in an aqueous system and used as a highly reactive intermediate for coupling with diverse natural products under very mild conditions. These include flavonoids, hydroxynaphthalenes, coumarins, xanthones, anthraquinones, phloroglucinols, phenolic acids, indole derivatives, tyrosine analogues, and quinolines. The clavatol moiety was mainly attached via C-C bonds to the ortho- or para-positions of phenolic hydroxyl/amino groups and the C2-position of the indole ring.

PubMedSearch : Liao_2020_J.Org.Chem_85_1298
PubMedID: 31860310
Gene_locus related to this paper: pencr-clae , pencr-clah

Related information

Gene_locus pencr-clae    pencr-clah

Citations formats

Liao G, Fan J, Ludwig-Radtke L, Backhaus K, Li SM (2020)
Increasing Structural Diversity of Natural Products by Michael Addition with ortho-Quinone Methide as the Acceptor
J Org Chem 85 :1298

Liao G, Fan J, Ludwig-Radtke L, Backhaus K, Li SM (2020)
J Org Chem 85 :1298