Covering: July 2012 to June 2015. Previous review: Nat. Prod. Rep., 2013, 30, 869–915 The
structurally diverse imidazole-, oxazole-, and thiazole-containing secondary metabolites are …

V-ATPase has recently emerged as a promising novel anticancer target based on extensive
in vitro and in vivo studies with the archazolids, complex polyketide macrolides which …

This is a review of papers published in the year 2015 that focus on the synthesis, reactivity,
or properties of compounds containing a carbon-transition metal double or triple bond …

A convergent synthesis of a C 1–C 23 fragment of the archazolids has been completed
based on a high-yielding Stille coupling to construct the substituted Z, Z, E-conjugated …

This chapter describes olefin cross‐metathesis (CM) reactions catalyzed by ruthenium,
molybdenum, and tungsten complexes and surveys the literature from 1993 through 2020 …

An archazolid natural product fragment that displays dose-dependent inhibition of the
vacuolar-type ATPase (VATPase) has been synthesized by a high-yielding Suzuki coupling …

The archazolids are a family of natural products that display powerful growth inhibitory
activity against a number of human cancer cell lines. This activity has been linked to …

8.6 Derivatization of Archazolid A (2) and B (3) Page 245 8.6. Derivatization of Archazolid A (
2 ) and B ( 3 ) 8.6 Derivatization of Archazolid A (2) and B (3) 8.6. 1 Semi-Synthesis of …