CS2/KOH System-Promoted Stereoselective Synthesis of (E)-Alkenes from Diarylalkynes and a "Hidden" Zinin-Type Reduction of Nitroarenes into Arylamines.

In this work, we present the CS2/KOH system as a practical and efficient reductive medium for obtaining (E)-alkenes from alkynes through a highly stereoselective semireduction reaction. This cost-effective system enabled successful semireduction reactions of diverse alkynes using water as a hydrogen source, yielding moderate to excellent yields. The versatility of this protocol is further demonstrated through the synthesis of relevant compounds such as pinosylvin and resveratrol precursors, along with the notable anticancer agent DMU-212. Furthermore, during the reaction scope investigation, we serendipitously disclosed that this reductive system was also able to promote a Zinin-type reaction to reduce nitroarenes into arylamines.

Palladium-Catalyzed Direct Selanylation of Chalcogenophenes and Arenes Assisted by 2-(Methylthio)amide.

The direct and selective conversion of a C-H bond into a C-Se bond remains a significant challenge, which is even more intricate with substrates having an innate regioselectivity under several reaction conditions, such as chalcogenophenes. We overrode their selectivity toward selanylation using palladium, copper, and the 2-(methylthio)amide directing group. This chelation-assisted direct selanylation was also suitable for mono and double ortho functionalization of arenes. The mechanistic studies indicate high-valent Pd(IV) species in the catalytic cycle, a reversible C-H activation step, and Cu(II) as a sequestering agent for organoselenide byproducts.

Copper-Mediated Intramolecular Interrupted CuAAC Selanylation.

We, herein, describe a copper-mediated domino CuAAC intramolecular selanylation for the synthesis of unprecedented fused benzo[4,5][1,3]selenazolo[3,2-c][1,2,3]triazoles from 1,2-bis(2-azidoaryl)diselenides and terminal alkynes under microwave irradiation. This is the seminal method for the synthesis of these fused heterocycles, and it proceeds under mild conditions, tolerates several functional groups, and can be carried out using environmentally benign solvents such as dimethyl carbonate. This transformation has been successfully extended to TMS-protected alkynes and to bioactive alkynes. A plausible reaction mechanism is proposed based on several control experiments and previous reports.

Silver-catalyzed direct selanylation of indoles: synthesis and mechanistic insights.

Herein we describe the Ag(i)-catalyzed direct selanylation of indoles with diorganoyl diselenides. The reaction gave 3-selanylindoles with high regioselectivity and also allowed direct access to 2-selanylindoles when the C3 position of the indole ring was blocked via a process similar to Plancher rearrangement. Experimental analyses and density functional theory calculations were carried out in order to picture the reaction mechanism. Among the pathways considered (via concerted metalation-deprotonation, Ag(iii), radical, and electrophilic aromatic substitution), our findings support a classic electrophilic aromatic substitution via Lewis adducts between Ag(i) and diorganoyl diselenides. The results also afforded new insights into the interactions between Ag(i) and diorganoyl diselenides.

Transition metal catalysed direct sulfanylation of unreactive C-H bonds: an overview of the last two decades.

Transition metal catalysed direct sulfanylations of unreactive C-H bonds have become a unique and straightforward synthetic strategy in late-stage C-S bond formation of relevant complex molecules. Such transformations represent a breakthrough in modern synthetic organic chemistry, as they offer unusual reactivity patterns and avoid pre-functionalization of the starting materials. Despite inherent challenges in activating/functionalizing unreactive C-H bonds, a considerable number of different transition metals have shown the ability to selectively catalyze these processes toward C-S bond formation. In this sense, this review article covers the development and mechanistic analysis of the direct sulfanylation of Csp3-H and Csp2-H bonds through transition metal catalysed reactions in the last two decades, providing an essential guide for organic chemists working on this research area.

Crystal structures of 3-halo-2-organochalcogenylbenzo[b]chalcogenophenes.

The structure of the title compounds 3-bromo-2-(phenyl-sulfan-yl)benzo[b]thiophene (C14H9BrS2; 1), 3-iodo-2-(phenyl-sulfan-yl)benzo[b]thio-phene (C14H9IS2; 2), 3-bromo-2-(phenyl-selan-yl)benzo[b]seleno-phene (C14H9BrSe2; 3), and 3-iodo-2-(phenyl-selan-yl)benzo[b]seleno-phene (C14H9ISe2; 4) were determined by single-crystal X-ray diffraction; all structures presented monoclinic (P21/c) symmetry. The phenyl group is distant from the halogen atom to minimize the steric hindrance repulsion for all structures. Moreover, the structures of 3 and 4 show an almost linear alignment of halogen-selenium-carbon atoms arising from the intra-molecular orbital inter-action between a lone pair of electrons on the halogen atom and the anti-bonding σ*Se-C orbital (n halogen→σ*Se-C). This inter-action leads to significant differences in the three-dimensional packing of the mol-ecules, which are assembled through π-π and C-H⋯π inter-actions. These data provide a better comprehension of the inter-molecular packing in benzo[b]chalcogenophenes, which is relevant for optoelectronic applications.

Light-Mediated Seleno-Functionalization of Organic Molecules: Recent Advances.

Organoselenium compounds constitute an important class of substances with applications in the biological, medicinal and material sciences as well as in modern organic synthesis, attracting considerable attention from the scientific community. Therefore, the construction of the C-Se bond via facile, efficient and sustainable strategies to access complex scaffolds from simple substrates are an appealing and hot topic. Visible light can be regarded as an alternative source of energy and is associated with environmentally-friendly processes. Recently, the use of visible-light mediated seleno-functionalization has emerged as an ideal and powerful route to obtain high-value selenylated products, with diminished cost and waste. This approach, involving photo-excited substrates/catalyst and single-electron transfer (SET) between substrates in the presence of visible light has been successfully used in the versatile and direct insertion of organoselenium moieties in activated and unactivated C(sp3 )-H, C(sp2 )-H, C(sp)-H bonds as well as C-heteroatom bonds. In most cases, ease of operation and accessibility of the light source (LEDs or commercial CFL bulbs) makes this approach more attractive and sustainable than the traditional strategies.

Trithiocarbonate Anion as a Sulfur Source for the Synthesis of 2,5-Disubstituted Thiophenes and 2-Substituted Benzo[b]thiophenes.

The trithiocarbonate anion (CS32-) was generated in situ from CS2 and KOH in dimethyl sulfoxide by a simple method and used as a novel synthetic equivalent of the S2- synthon for the synthesis of 2,5-disubstituted thiophenes from 1,3-butadiynes. Additionally, this system was employed for the metal-free synthesis of 2-substituted benzo[b]thiophenes from 2-haloalkynyl (hetero)arenes. These compounds were obtained from a cheap and readily available sulfur source in moderate to good yields, with good functional group tolerance.

Transition metal catalysed direct selanylation of arenes and heteroarenes.

Transition metal catalysed C-H functionalization has reached an exciting level of sophistication, and, today, it represents a paradigm shift from the standard logic of synthetic chemistry. The direct conversion of C-H bonds into C-heteroatoms remains, however, a critical challenge. Nowadays, there is a great demand in general synthetic chemistry in, for example, the materials science for the development of straightforward C-Se bond formation, in order to fulfil the practical requirements. In this sense, this review summarizes recent outstanding advances in the C-Se bond formation through transition metal-catalysed direct selanylation, providing new insights into their mechanistic aspects and disclosing effective synthetic routes with high atom economy. In addition, this review intends to show the growing opportunities to construct complex chemical scaffolds containing selenium atoms.

Correction: Dipolar vinyl sulfur fluorescent dyes. Synthesis and photophysics of sulfide, sulfoxide and sulfone based D-π-A compounds.

[This corrects the article DOI: 10.1039/C6RA27989A.].

Palladium-catalyzed direct arylation of selenophene.

An efficient and convenient method was developed for the regioselective formation of 2-aryl- or 2,5-diarylselenophenes via a palladium-catalyzed direct arylation. This protocol is suitable for a wide range of aryl halides containing different functional groups. The 2-arylated substrates can undergo an additional regioselective direct arylation event furnishing symmetrical or unsymmetrical 2,5-diaryl selenophenes in good yield. Competition experiments and the role of the acid additive are in agreement with a concerted metalation deprotonation (CMD) pathway.