Covering: 2010–2011. Previous review: Nat. Prod. Rep. 2010, 27, 1630–1680This review
covers the literature on simple indole alkaloids and those with a non-rearranged …

Abstract Optically pure 1, 2-diols and 1, 3-diols are the most privileged structural motifs,
widely present in natural products, pharmaceuticals and chiral auxiliaries or ligands …

Discovered as a modulator of the toxic response to environmental pollutants, aryl
hydrocarbon receptor (AhR) has recently gained attention for its involvement in various …

A method for the catalytic, enantioselective, carbosulfenylation of alkenes to construct 3, 4-
disubstituted chromans is described. Alkene activation proceeds through the intermediacy of …

A novel amide alkaloid, bursatamide A (1), featuring an unprecedented propyl-
hexahydronaphthalene carbon framework, was isolated from the infrequently studied sea …

To investigate the significance of antibiotics for the producing organism (s) in the natural
habitat, we screened a specimen of the fungicolous fungus Trichoderma phellinicola (syn …

The bursatellin-oxazinin family is a series of tyrosine-derived, nitrile-containing marine
natural products from gastro-pod and bivalve molluscs. Although the first analogs were …

Alkene aminooxygenation reactions provide vicinal amino alcohol derivatives, moieties that
frequently appear in catalysts, drugs, and other valuable molecules. This Chapter reviews …

A highly efficient asymmetric allylic substitution of Morita–Baylis–Hillman (MBH) carbonates
with phosphorus ylides under the catalysis of modified cinchona alkaloids was developed …

The enantioselective total syntheses of natural marine toxins, oxazinin-1,-2,-4,-5,-6 and
linear precursor preoxazinin-7 are described. The synthetic highlights include Sharpless …