A new species of the Pristimantis orestes group (Amphibia: Strabomantidae) from the high Andes of Ecuador, Reserva Mazar.

We describe a new Pristimantis from La Libertad and Rumiloma, Reserva Mazar, Andes of Southeastern Ecuador, at elevations between 2895-3415 m. This species is assigned to the P. orestes group, from whose members it differs by its small body size (adult males ≤ 18.1 mm; adult females ≤ 23.7 mm), usually reticulated ventral pattern, and visible tympanum. The vocalization of the new species consists of a series of calls; each call is composed by a pulsed, non-modulated note in frequency, and with a dominant frequency of 3122-3171 Hz. A molecular phylogeny based on a fragment of the mitochondrial gene 12S shows that the new species is sister to Pristimantis simonbolivari.

Communic acids: occurrence, properties and use as chirons for the synthesis of bioactive compounds.

Communic acids are diterpenes with labdane skeletons found in many plant species, mainly conifers, predominating in the genus Juniperus (fam. Cupresaceae). In this review we briefly describe their distribution and different biological activities (anti- bacterial, antitumoral, hypolipidemic, relaxing smooth muscle, etc.). This paper also includes a detailed explanation of their use as chiral building blocks for the synthesis of bioactive natural products. Among other uses, communic acids have proven useful as chirons for the synthesis of quassinoids (formal), abietane antioxidants, ambrox and other perfume fixatives, podolactone herbicides, etc., featuring shorter and more efficient processes.

Use of the plant Bellardia trixago for the enantiospecific synthesis of odorant products.

An easy procedure to obtain extracts enriched in trixagol monomalonylesther (1) from aerial parts of the plant Belladia trixago chemotype Trix was developed. Preparation of (+)-dihydro-gamma-ionone (4) was carried out directly from the extracts with good yields by selective oxidation. Other interesting odorant products as alpha-ambrinol (5), ambraldehyde (6) and the tricyclic compound 7 were synthesized very efficiently using (4) as intermediate.