Organic & Biomolecular Chemistry Blog

In this HOT OBC paper from the ‘Nucleic acids: new life, new materials’ web collection, short and high-yielding syntheses for the nucleobases preQ1 base, Q base, and (ent)-Q base are described based on cheap and readily available starting compounds. For the latter two bases, Hans-Dieter Gerber and Gerhard Klebe use preQ1 as a central synthon and nucleophilic substitution reactions with appropriately decorated halocyclopentenyl synthons to produce the desired bases.

For the detailed discussion and reaction analysis download the paper, it is free to do so for 4 weeks!

Concise and efficient syntheses of preQ1 base, Q base, and (ent)-Q base
Hans-Dieter Gerber and Gerhard Klebe
DOI: 10.1039/C2OB26387D

Liked that? Then why not have a look at the rest of the ‘Nucleic acids: new life, new materials’ web collection.

In this HOT paper Michael J. Porter and colleagues at University College London report the synthesis of the core structure of tagetitoxin using a novel photochemical 1,2-Stevens rearrangement. The method presented by Porter et al. uses the carbene-mediated ring expansion of a bicyclic monothioacetal, through the intermediacy of a sulfonium ylide.

To see all the experimental and mechanistic details download the paper today. It will be free to access for 4 weeks!

Inter- and intramolecular reactions of 1-deoxy-1-thio-1,6-anhydrosugars with α-diazoesters: synthesis of the tagetitoxin core by photochemical ylide rearrangement
Anne J. Price Mortimer, Julien R. H. Plet, Oluwafunsho A. Obasanjo, Nikolas Kaltsoyannis and Michael J. Porter
DOI: 10.1039/C2OB26308D

In this HOT Communication Patrick J. Hrdlicka and colleagues at University of Idaho study the hybridization properties of oligonucleotides, which are modified with 5-(1-aryl-1,2,3-triazol-4-yl)-2′-deoxyuridine monomers featuring three differentially sized aromatic moieties at the 1-position of the triazole ring.

These modified oligonucleotides modified with consecutive show a strong thermal affinity and binding specificity toward RNA targets, due to the formation of stabilizing chromophore arrays in the major groove.

This Communication can be downloaded for free for 4 weeks.

This work is also part of the OBC collection on ‘Nucleic acids: new life, new materials‘, so for related articles have a browse through the collection.

Synthesis and hybridization properties of oligonucleotides modified with 5-(1-aryl-1,2,3-triazol-4-yl)-2′-deoxyuridines
Mamta Kaura, Pawan Kumar and Patrick J. Hrdlicka
DOI: 10.1039/C2OB26717A

In this HOT Communication Adam R. Urbach and colleagues, Trinity University, present a convenient approach for the quantitative removal of the synthetic host cucurbit[8]uril from aqueous mixtures using a sepharose resin coated in memantine groups to selectively isolate cucurbit[8]uril in the presence of competing hosts and guests. The “cucurbit[8]uril sponge” can separate cucurbit[8]uril from cucurbit[6]uril and reverse the cucurbit[8]uril-mediated dimerization of peptides.

This communication is free to access for the next 4 weeks!

A cucurbit[8]uril sponge
Vijayakumar Ramalingam, Sharon K. Kwee, Lisa M. Ryno and Adam R. Urbach
DOI: 10.1039/C2OB26774H

In this OBC HOT article Shengming Ma and co-workers report the efficient synthesis of N-(buta-2,3-dienyl) amides and their application towards the efficient synthesis of oxazolines under palladium catalysis.

Read the article to find out more about the reaction conditions and yields involved in this synthesis…. FREE to access for 4 weeks!

Efficient synthesis of N-(buta-2,3-dienyl) amides from terminal N-propargyl amides and their synthetic potential towards oxazoline derivatives
Bo Chen, Nan Wang, Wu Fan and Shengming Ma
DOI: 10.1039/C2OB26291F