4467-06-5Relevant articles and documents
Bottom-Up Construction of Mesoporous Nanotubes from 78-Component Self-Assembled Nanobarrels
Zhang, Guang-Lu,Zhou, Li-Peng,Yuan, Da-Qiang,Sun, Qing-Fu
, p. 9844 - 9848 (2015)
Segmental and continuous hexagonal-packed mesoporous metal-organic nanotubes (MMONTs) with outside diameters of up to 4.5 nm and channel sizes of 2.4 nm were hierarchically constructed by a rational multicomponent self-assembly process involving starting from [L2Pd2(NO3)2] (L=o-phenanthroline or 2,2′-bipyridine) and 4-pyridinyl-3-pyrazole. An unprecedented crystallization-driven cross-linking between discrete nanobarrel building units by spontaneous loss of the capping ligands to form infinite nanotubes was observed. Such a barrel-to-tube transformation provides new possibilities for the fabrication of MMONTs using the solution bottom-up approach.
Organocatalytic synthesis of (Het)biaryl scaffoldsviaphotoinduced intra/intermolecular C(sp2)-H arylation by 2-pyridone derivatives
Das, Tapas Kumar,Kundu, Mrinalkanti,Mondal, Biswajit,Ghosh, Prasanjit,Das, Sajal
, p. 208 - 218 (2021/12/29)
A uniqueN,O-bidentate ligand 6-oxo-1,6-dihydro-pyridone-2-carboxylic acid dimethylamide (L1) catalyzed direct C(sp2)-H (intra/intermolecular) arylation of unactivated arenes has been developed to expedite access to (Het)biaryl scaffolds under UV-irradiation at room temperature. The protocol tolerated diverse functional groups and substitution patterns, affording the target products in moderate to excellent yields. Mechanistic investigations were also carried out to better understand the reaction pathway. Furthermore, the synthetic applicability of this unified approach has been showcasedviathe construction of biologically relevant 4-quinolone, tricyclic lactam and sultam derivatives.
Base-Activated Latent Heteroaromatic Sulfinates as Nucleophilic Coupling Partners in Palladium-Catalyzed Cross-Coupling Reactions
Blakemore, David C.,Cook, Xinlan A. F.,Moses, Ian B.,Pantaine, Lo?c R. E.,Sach, Neal W.,Shavnya, Andre,Willis, Michael C.
, p. 22461 - 22468 (2021/09/09)
Heteroaromatic sulfinates are effective nucleophilic reagents in Pd0-catalyzed cross-coupling reactions with aryl halides. However, metal sulfinate salts can be challenging to purify, solubilize in reaction media, and are not tolerant to multi-step transformations. Here we introduce base-activated, latent sulfinate reagents: β-nitrile and β-ester sulfones. We show that under the cross-coupling conditions, these species generate the sulfinate salt in situ, which then undergo efficient palladium-catalyzed desulfinative cross-coupling with (hetero)aryl bromides to deliver a broad range of biaryls. These latent sulfinate reagents have proven to be stable through multi-step substrate elaboration, and amenable to scale-up.