Stereoselective Synthesis of 1-Tuberculosinyl Adenosine; a Virulence Factor of Mycobacterium tuberculosis.

Despite its status as one of the world's most prevalent and deadly bacterial pathogens, Mycobacterium tuberculosis (Mtb) infection is not routinely diagnosed by rapid and highly reliable tests. A program to discover Mtb-specific biomarkers recently identified two natural compounds, 1-tuberculosinyl adenosine (1-TbAd) and N(6)-tuberculosinyl adenosine (N(6)-TbAd). Based on their association with virulence, the lack of similar compounds in nature, the presence of multiple stereocenters, and the need for abundant products to develop diagnostic tests, synthesis of these compounds was considered to be of high value but challenging.

AIM and NPA studies of the role of polarization in electronic structures.

Atomic charges, as measured by Atoms in Molecule (AIM) or Natural Population Analyses (NPA), of the enolate anions of acetaldehyde and crotonaldehyde and of pentadienyl anion and cation show both charge transfer and polarization effects. In general, normal resonance structures and "curved arrow" symbolism give good representations of π-electron distributions, but back-polarizations in the σ-system complicate these electronic structures and can obscure the correspondence to resonance symbols. Twisting a vinyl group to orthogonality disrupts the π-system, but the vinyl group retains significant charge transfers and polarizations.