Literature DB >> 25137016

Recent developments in transition metal-catalysed spiroketalisation.

Rachelle Quach1, Daniel F Chorley, Margaret A Brimble.   

Abstract

The spiroketal motif occurs in a wide range of biologically active natural products and represents a valuable target in medicinal chemistry and total synthesis. In recent years, innovative new synthetic methods have substantially expanded the range of potential precursors, cyclisation modes and opportunities for asymmetric catalysis and tandem processes. This Perspective aims to highlight recent rapid advances in the use of transition metal catalysis for spiroketal formation, in the context of our own investigations into gold-catalysed asymmetric spiroketalisation.

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Year:  2014        PMID: 25137016     DOI: 10.1039/c4ob01325e

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  2 in total

1.  Stereocontrolled Synthesis of Spiroketals: An Engine for Chemical and Biological Discovery.

Authors:  Alyssa L Verano; Derek S Tan
Journal:  Isr J Chem       Date:  2017-03-10       Impact factor: 3.333

2.  Blue light photoredox-catalysed acetalation of alkynyl bromides.

Authors:  Xue-Li Lyu; Shi-Sheng Huang; Hong-Jian Song; Yu-Xiu Liu; Qing-Min Wang
Journal:  RSC Adv       Date:  2019-11-06       Impact factor: 4.036

  2 in total

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