Lactones: Classification, synthesis, biological activities, and industrial applications

SK Sartori, MAN Diaz, G Diaz-Muñoz - Tetrahedron, 2021 - Elsevier
This review summarizes the current knowledge on lactones, a class of biologically active
natural products isolated from a wide range of living organisms. Butenolide, 5, 6 …

Are Alkyne Reductions Chemo-, Regio-, and Stereoselective Enough To Provide Pure (Z)-Olefins in Polyfunctionalized Bioactive Molecules?

C Oger, L Balas, T Durand, JM Galano - Chemical reviews, 2013 - ACS Publications
Many biologically active molecules incorporate carbon− carbon double bond (s) with well-
defined configurations (E or Z), such as β-carotene, 1 polyene antifungal drugs, 2, 3 …

Marine natural products

JW Blunt, BR Copp, MHG Munro, PT Northcote… - Natural product …, 2004 - pubs.rsc.org
Covering: 2002. Previous review: Nat. Prod. Rep., 2003, 20, 1 This review covers the
literature published in 2002 for marine natural products, with 579 citations (413 for the …

Macrolactonizations in the total synthesis of natural products

A Parenty, X Moreau, JM Campagne - Chemical reviews, 2006 - ACS Publications
Ever since the first isolation of Exaltolide 1 (Figure 1) in 1927 by Kerschbaum, 1 interest in
macrocyclic lactones, defined as lactones with more than 8 atoms in the ring, has been …

<? ACS-CT-START-Insert?> Update 1 of:<? ACS-CT-END-Insert?> Macrolactonizations in the Total Synthesis of Natural Products

A Parenty, X Moreau, G Niel, JM Campagne - Chemical Reviews, 2013 - ACS Publications
1. INTRODUCTION Ever since the first isolation of Exaltolide 1 (Figure 1) in 1927 by
Kerschbaum, 1 interest in macrocyclic lactones, defined as lactones with more than 8 atoms …

Marine-derived macrolides 1990–2020: An overview of chemical and biological diversity

H Zhang, J Zou, X Yan, J Chen, X Cao, J Wu, Y Liu… - Marine Drugs, 2021 - mdpi.com
Macrolides are a significant family of natural products with diverse structures and
bioactivities. Considerable effort has been made in recent decades to isolate additional …

Stereoselective semi‐hydrogenations of alkynes by first‐row (3d) transition metal catalysts

BJ Gregori, MOWS Schmotz… - …, 2022 - Wiley Online Library
The chemo‐and stereoselective semi‐hydrogenation of alkynes to alkenes is a fundamental
transformation in synthetic chemistry, for which the use of precious 4d or 5d metal catalysts …

Formal total synthesis of oximidine II via a Suzuki-type cross-coupling macrocyclization employing potassium organotrifluoroborates

GA Molander, F Dehmel - Journal of the American Chemical …, 2004 - ACS Publications
A formal total synthesis of oximidine II has been achieved, employing a Suzuki-type coupling
approach to construct the highly strained, polyunsaturated 12-membered macrolactone. To …

Atom economic macrolactonization and lactonization via redox-neutral rhodium-catalyzed coupling of terminal alkynes with carboxylic acids

A Lumbroso, N Abermil, B Breit - Chemical Science, 2012 - pubs.rsc.org
Atom economic macrolactonization and lactonization via redox-neutral rhodium-catalyzed
coupling of terminal alkynes with carboxylic acids - Chemical Science (RSC Publishing) DOI:10.1039/C2SC00812B …

Sesterterpenoids

Y Liu, L Wang, JH Jung, S Zhang - Natural Product Reports, 2007 - pubs.rsc.org
Sesterterpenoids - Natural Product Reports (RSC Publishing) DOI:10.1039/B617259H Royal
Society of Chemistry View PDF VersionPrevious ArticleNext Article DOI: 10.1039/B617259H …