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Themed collection New Directions in Natural Product Synthesis

15 items
Editorial

New directions in natural product synthesis

Guest Editors Huw M. L. Davies, Kenichiro Itami and Brian M. Stoltz introduce this themed issue on natural product synthesis.

Graphical abstract: New directions in natural product synthesis
From the themed collection: New Directions in Natural Product Synthesis
Review Article

Recent applications of C–H functionalization in complex natural product synthesis

In this review, recent examples featuring C–H functionalization in the synthesis of complex natural products are discussed.

Graphical abstract: Recent applications of C–H functionalization in complex natural product synthesis
From the themed collection: New Directions in Natural Product Synthesis
Review Article

Application of (4+3) cycloaddition strategies in the synthesis of natural products

This review summarizes the applications of (4+3) cycloadditions, both classical and formal, in the syntheses of natural products in the last two decades.

Graphical abstract: Application of (4+3) cycloaddition strategies in the synthesis of natural products
From the themed collection: New Directions in Natural Product Synthesis
Review Article

Aryne-based strategy in the total synthesis of naturally occurring polycyclic compounds

This review has outlined the strategies and tactics of using arynes in the total syntheses of polycyclic natural products.

Graphical abstract: Aryne-based strategy in the total synthesis of naturally occurring polycyclic compounds
From the themed collection: New Directions in Natural Product Synthesis
Review Article

Oxidative coupling strategies for the synthesis of indole alkaloids

Direct functionalization of indole through oxidative coupling reactions with enolates or phenols provides a powerful tool for assembling indole alkaloids.

Graphical abstract: Oxidative coupling strategies for the synthesis of indole alkaloids
From the themed collection: New Directions in Natural Product Synthesis
Open Access Review Article

Amide activation: an emerging tool for chemoselective synthesis

This review focusses on the use of amide activation for chemoselective functionalisation and its application in natural product synthesis.

Graphical abstract: Amide activation: an emerging tool for chemoselective synthesis
From the themed collection: New Directions in Natural Product Synthesis
Review Article

Recent advances in chemical dearomatization of nonactivated arenes

A comprehensive review of recent developments and applications of dearomatization of simple, nonactivated aromatic compounds.

Graphical abstract: Recent advances in chemical dearomatization of nonactivated arenes
From the themed collection: New Directions in Natural Product Synthesis
Review Article

Enabling strategies for step efficient syntheses

The field of natural product total synthesis has reached the point where synthetic efficiency has become more important than merely defining a viable (yet less ideal) route to the target molecule. Several synthesis of different types of natural products are compared using color-coded flow charts.

Graphical abstract: Enabling strategies for step efficient syntheses
From the themed collection: New Directions in Natural Product Synthesis
Review Article

Gold-catalyzed glycosylation in the synthesis of complex carbohydrate-containing natural products

Gold(I)- and gold(III)-catalyzed glycosylation reactions and their application in the synthesis of natural glycoconjugates are reviewed.

Graphical abstract: Gold-catalyzed glycosylation in the synthesis of complex carbohydrate-containing natural products
From the themed collection: New Directions in Natural Product Synthesis
Review Article

Recent advances in the application of Diels–Alder reactions involving o-quinodimethanes, aza-o-quinone methides and o-quinone methides in natural product total synthesis

This review summarizes recent advances in Diels–Alder reactions involving o-QDMs, o-QMs and aza-o-QMs. The power and potential of this strategy in organic synthesis and natural product total synthesis is highlighted.

Graphical abstract: Recent advances in the application of Diels–Alder reactions involving o-quinodimethanes, aza-o-quinone methides and o-quinone methides in natural product total synthesis
From the themed collection: New Directions in Natural Product Synthesis
Tutorial Review

Beyond olefins: new metathesis directions for synthesis

This tutorial review provides an introduction to metathesis reactions between carbonyls and olefins or alkynes and their application in natural product synthesis.

Graphical abstract: Beyond olefins: new metathesis directions for synthesis
From the themed collection: New Directions in Natural Product Synthesis
Tutorial Review

Metamorphosis of cycloalkenes for the divergent total synthesis of polycyclic indole alkaloids

This review summarizes the divergent synthesis of monoterpene indole alkaloids using cycloalkene as the turning point of structural diversity.

Graphical abstract: Metamorphosis of cycloalkenes for the divergent total synthesis of polycyclic indole alkaloids
From the themed collection: New Directions in Natural Product Synthesis
Tutorial Review

Radicals in natural product synthesis

Free radical intermediates have intrigued chemists since their discovery, and an ever-increasing appreciation for their unique reactivity has resulted in the widespread utilization of these species for natural product synthesis.

Graphical abstract: Radicals in natural product synthesis
From the themed collection: New Directions in Natural Product Synthesis
Tutorial Review

Computational chemistry strategies in natural product synthesis

Computational chemistry has made profound contributions to natural product synthesis, as showcased in several impressive examples.

Graphical abstract: Computational chemistry strategies in natural product synthesis
From the themed collection: New Directions in Natural Product Synthesis
Tutorial Review

Questions in natural products synthesis research that can (and cannot) be answered using computational chemistry

Questions of relevance to synthetic chemists that can be answered, at least in part, using quantum chemical computations are highlighted.

Graphical abstract: Questions in natural products synthesis research that can (and cannot) be answered using computational chemistry
From the themed collection: New Directions in Natural Product Synthesis
15 items

About this collection

We are delighted to present a Chemical Society Reviews themed collection on ‘New enabling strategies for natural products synthesis’. This issue, guest edited by Brian Stoltz (California Institute of Technology), Ken Itami (Nagoya University) and Huw M. L. Davies (Emory University), focusses on new enabling methodologies and their applications to the synthesis of complex natural products. The collection aims to highlight the major advances that have been made to streamline the synthesis of complex targets, as well as showcase the high level of innovation that drives complex synthesis and the value of natural product applications.

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