The generation of metal carbenes from readily available alkynes represents a significant advance in metal carbene chemistry. However, most of these transformations are based on the use of noble-metal catalysts and successful examples of such an asymmetric version are still very scarce. Here a copper-catalyzed enantioselective cascade cyclization of -propargyl ynamides is reported, enabling the practical and atom-economical construction of diverse chiral polycyclic pyrroles in generally good to excellent yields with wide substrate scope and excellent enantioselectivities (up to 97:3 e.r.). Importantly, this protocol represents the first copper-catalyzed asymmetric diyne cyclization. Moreover, mechanistic studies revealed that the generation of donor/donor copper carbenes is presumably involved in this 1,5-diyne cyclization, which is distinctively different from the related gold catalysis, and thus it constitutes a novel way for the generation of donor/donor metal carbenes.
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http://dx.doi.org/10.1021/jacs.9b09303 | DOI Listing |
Org Lett
December 2024
Department of Chemistry, University of California, Davis, One Shields Avenue, Davis, California 95616, United States.
Two routes to assemble the complete tricyclic core of alopecurone C are described. In the first-generation route, an efficient synthesis of the "eastern" half of the target, including a decagram-scale rhodium-catalyzed C-H insertion reaction, was developed. When this route proved intractable for assembling the final flavanone ring, a successful second-generation route was developed from a flavanone precursor (naringenin) employing a later stage C-H insertion.
View Article and Find Full Text PDFChem Asian J
November 2024
Department of Chemistry, Laboratory of Organic Synthesis & Catalysis, Indian Institute of Technology Roorkee, Roorkee, Uttarakhand, 247667, India.
The donor-donor carbene chemistry field is underdeveloped and often relies on harsh reaction conditions, utilizing either thermal or oxidative process with or without transition-metal catalysts. In this review, we discussed the synthesis and transformation of donor-donor diazo compounds from N-sulfonylhydrazones in the presence of light and base. The N-sulfonylhydrazones are easily accessible from the corresponding carbonyl compounds and sulfonyl hydrazides through condensation.
View Article and Find Full Text PDFChem Sci
November 2024
Department of Chemistry, University of California One Shields Avenue Davis California 95616 USA
[This corrects the article DOI: 10.1039/D3SC00734K.].
View Article and Find Full Text PDFACS Appl Mater Interfaces
October 2024
Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Hong Kong 310028, PR China.
Nat Mater
May 2024
College of Materials Science and Opto-Electronic Technology, University of Chinese Academy of Sciences, Beijing, People's Republic of China.
π-Conjugated polymers (CPs) have broad applications in high-performance optoelectronics, energy storage, sensors and biomedicine. However, developing green and efficient methods to precisely synthesize alternating CP structures on a large scale remains challenging and critical for their industrialization. Here a room-temperature, scalable and homogeneous Suzuki-Miyaura-type polymerization reaction is developed with broad generality validated for 24 CPs including donor-donor, donor-acceptor and acceptor-acceptor connectivities, yielding device-quality polymers with high molecular masses.
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