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 …

Evolution of dithiane-based strategies for the construction of architecturally complex natural products

AB Smith, CM Adams - Accounts of chemical research, 2004 - ACS Publications
Umpolung-based strategies play a significant role in organic synthesis. Particularly
important are 1, 3-dithiane linchpins, which serve as convenient acyl anion equivalents. The …

Advances in the total synthesis of biologically important marine macrolides

KS Yeung, I Paterson - Chemical reviews, 2005 - ACS Publications
Marine organisms, particularly sponge invertebrates and associated bacteria, are
enormously rich sources of structurally diverse secondary metabolites with unique molecular …

The role of 1, 3-dithianes in natural product synthesis

M Yus, C Nájera, F Foubelo - Tetrahedron, 2003 - Elsevier
The normal reactivity of a carbonyl compound (I) is as an a 1-reagent (II) and the temporary
reversal of the characteristic pattern of reactivity of a functional group is described by the …

<? 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 …

Selective monodeprotection of bis-silyl ethers

RD Crouch - Tetrahedron, 2004 - Elsevier
As synthetic targets have grown more complex, protection/deprotection protocols have
assumed prominent roles in synthetic organic chemistry. 1–3 The ability to efficiently protect …

Actin‐binding marine macrolides: Total synthesis and biological importance

KS Yeung, I Paterson - Angewandte Chemie International …, 2002 - Wiley Online Library
Marine organisms produce a fascinating range of structurally diverse secondary metabolites,
which often possess unusual and sometimes unexpected biological activities. This structural …

Hydroxyl-directed stereoselective diboration of alkenes

TP Blaisdell, TC Caya, L Zhang… - Journal of the …, 2014 - ACS Publications
An alkoxide-catalyzed directed diboration of alkenyl alcohols is described. This reaction
occurs in a stereoselective fashion and is demonstrated with cyclic and acyclic homoallylic …

Evolution of anion relay chemistry: construction of architecturally complex natural products

Y Deng, AB Smith III - Accounts of chemical research, 2020 - ACS Publications
Multicomponent union tactics in which three or more fragments are rapidly connected are
highly prized in the construction of architecturally complex natural products. Anion Relay …

Anion Relay Enabled [3+ 3]-Annulation of Active Methylene Isocyanides and Ene-Yne-Ketones

J Dong, L Bao, Z Hu, S Ma, X Zhou, M Hao, N Li… - Organic …, 2018 - ACS Publications
A new anion relay enabled [3+ 3]-annulation of active methylene isocyanides and
conjugated ene-yne-ketones was developed for the efficient and straightforward synthesis of …