Fifteen years of biological and synthetic studies of decarestrictine family

VB Riatto, RA Pilli, MM Victor - Tetrahedron, 2008 - Elsevier
Decanolides have attracted special attention over the last years 1e3 and an important class
of compounds is the decarestrictine family. The decarestrictines are secondary metabolites …

A new strategy for efficient synthesis of medium and large ring lactones without high dilution or slow addition

W Zhao, Z Li, J Sun - Journal of the American Chemical Society, 2013 - ACS Publications
We have developed an efficient method for medium and large ring lactone synthesis by a
conceptually different ring-expansion strategy. The design of an unprecedented ring …

Synthesis of Eight‐Membered Lactones: Intermolecular [6+ 2] Cyclization of Amphoteric Molecules with Siloxy Alkynes

W Zhao, Z Wang, J Sun - Angewandte Chemie International Edition, 2012 - infona.pl
That's about the size of it: The title molecules react with siloxy alkynes in the presence of a
Brønsted acid to deliver medium‐sized lactones through a [6+ 2] cyclization (see scheme; …

An Evans− Tishchenko− Ring-Closing Metathesis Approach to Medium-Ring Lactones

JI Aird, AN Hulme, JW White - Organic letters, 2007 - ACS Publications
A new approach to the synthesis of medium-ring lactones is reported based on sequential
Evans− Tishchenko and ring-closing metathesis (RCM) reactions. High diastereoselectivity …

Total synthesis of LL-Z1640-2 utilizing a late-stage intramolecular Nozaki–Hiyama–Kishi reaction

CA LeClair, MB Boxer, CJ Thomas, DJ Maloney - Tetrahedron letters, 2010 - Elsevier
Total synthesis of LL-Z1640-2 utilizing a late-stage intramolecular Nozaki–Hiyama–Kishi
reaction - ScienceDirect Skip to main contentSkip to article Elsevier logo Journals & Books …

Total synthesis of (+)-herbarumin I via intermolecular Nozaki–Hiyama–Kishi reaction

AA Sabino, RA Pilli - Tetrahedron letters, 2002 - Elsevier
Total synthesis of (+)-herbarumin I via intermolecular Nozaki–Hiyama–Kishi reaction -
ScienceDirect Skip to main contentSkip to article Elsevier logo Journals & Books Search …

First total synthesis of modiolide A, based on the whole-cell yeast-catalyzed asymmetric reduction of a propargyl ketone

M Matsuda, T Yamazaki, K Fuhshuku, T Sugai - Tetrahedron, 2007 - Elsevier
While the first total synthesis of modiolide A (1a), a 10-membered ring lactone with a marine-
origin was achieved, an important chiral building block for constructing the chirality at C-4 in …

Convergent syntheses of 3, 6-dihydroxydec-4-enolides

JC Killen, LC Axford, SE Newberry, TJ Simpson… - Organic …, 2012 - ACS Publications
Convergent Syntheses of 3,6-Dihydroxydec-4-enolides | Organic Letters ACS ACS
Publications C&EN CAS Find my institution Log In Organic Letters ACS Publications. Most …

Protecting‐Group Directed Stereoselective Intramolecular Nozaki–Hiyama–Kishi Reaction: A Concise and Efficient Total Synthesis of Amphidinolactone A

DK Mohapatra, PP Das, MR Pattanayak, G Gayatri… - 2010 - Wiley Online Library
A convergent total synthesis of amphidinolactone A, a cytotoxic macrolide from the cultured
dinoflagellate Amphidinium sp., is described in 13 linear steps. The key step in the synthetic …

Synthesis of 9-and 10-membered macrolactones by selective ozonolysis of 1, 4-diazaphenanthrene derivatives

E Pérez-Sacau, J Soto-Delgado, A Estévez-Braun… - Tetrahedron, 2005 - Elsevier
9-and 10-membered macrolactones bearing benzo and diazine rings were obtained by
chemoselective ozonolysis of dihydrofuran and pyran 1, 4-diazaphenathrene derivatives …