98%
921
2 minutes
20
Bridged and fused rings are commonly found in biologically important molecules. Current tactics to construct these ring systems are primarily based on stepwise ring formation (i.e., making one ring first followed by making another) and cycloaddition reactions (e.g., Diels-Alder reaction). To seek a complementary and perhaps more unified ring-forming approach, a deconstructive strategy based on C-C bond activation of cyclic ketones has been conceived. The named "cut-and-sew" reaction uses cyclic ketones with a tethered unsaturated moiety as substrates, which involves oxidative addition of a transition metal into the ketone C-C bond followed by intramolecular insertion of the unsaturated unit. This strategy has proved successful to access diverse ring scaffolds that are nontrivial to construct otherwise.This Account offers a concise summary of our laboratory's systematic efforts in developing transition metal-catalyzed cut-and-sew reactions for the synthesis of bridged and fused rings over the past 10 years. In particular, we will focus on the reactions using readily available benzocyclobutenones and cyclobutanones. To date, the scope of the cut-and-sew reactions has been greatly expanded. First, diverse unsaturated moieties can serve as suitable coupling partners, such as alkenyl, alkynyl, allenyl, carbonyl, and iminyl groups. Second, a variety of reaction modes have been uncovered. In this account, (4 + 2), (4 + 2 - 1), and (4 + 1) cycloadditions that lead to a range of bridged or fused scaffolds will be summarized. Third, enantioselective transformations have been realized to efficiently construct chiral scaffolds, which are enabled by two strategies: enantio-determining migratory insertion and desymmetrization of cyclobutanones. Fourth, the synthetic applications have been demonstrated in streamlined total syntheses of a number of complex natural products. Compared to conventional synthetic logics, the cut-and-sew reaction allows the development of new bond-disconnecting strategies. Thus, the syntheses of (-)-cycloclavine, (-)-thebainone A, penicibilaenes, and the proposed cycloinumakiol are discussed in more detail.In addition to the narrative of the development of the cut-and-sew chemistry, this Account also aims to provide core guiding foundations and inspirations toward broader deconstructive synthetic applications through C-C bond cleavage. It is anticipated that more classes of cyclic compounds could serve as the substrates beyond benzocyclobutenones and cyclobutanones, and more diverse unsaturated moieties could be coupled. It can also be envisaged that more innovative utilization of this cut-and-sew strategy in complex organic syntheses will be revealed in the near future.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9386905 | PMC |
http://dx.doi.org/10.1021/acs.accounts.2c00400 | DOI Listing |
J Am Chem Soc
September 2025
Department of Chemistry, University of Chicago, Chicago, Illinois 60637, United States.
Transition metal-catalyzed "cut-and-sew" reactions offer an efficient approach to construct bridged and fused scaffolds; however, the substrates have been primarily restricted to cyclic ketones and activated cyclopropanes. Here we report the first cut-and-sew transformation between β-lactams and alkenes/alkynes via C-C bond activation. Diverse bridged and fused nitrogen-heterocycles are prepared using this method with good functional group tolerance.
View Article and Find Full Text PDFJ Cell Biol
September 2025
Department of Neuroscience, Yale University School of Medicine, New Haven, CT, USA.
BLTP2/KIAA0100, a bridge-like lipid transfer protein, was reported to localize at contacts of the ER with either the plasma membrane (PM) or recycling tubular endosomes depending on the cell type. Our findings suggest that mediating bulk lipid transport between the ER and the PM is a key function of this protein, as BLTP2 tethers the ER to tubular endosomes only after they become continuous with the PM and that it also tethers the ER to macropinosomes in the process of fusing with the PM. We further identify interactions underlying binding of BLTP2 to the PM, including phosphoinositides, the adaptor proteins FAM102A/FAM102B, and N-BAR domain proteins at membrane-connected tubules.
View Article and Find Full Text PDFIEEE J Biomed Health Inform
September 2025
Vision-language models (VLMs) have shown promise in 2D medical image analysis, but extending them to 3D remains challenging due to the high computational demands of volumetric data and the difficulty of aligning 3D spatial features with clinical text. We present Med3DVLM, a 3D VLM designed to address these challenges through three key innovations: (1) DCFormer, an efficient encoder that uses decomposed 3D convolutions to capture fine-grained spatial features at scale; (2) SigLIP, a contrastive learning strategy with pairwise sigmoid loss that improves image-text alignment without relying on large negative batches; and (3) a dual-stream MLP-Mixer projector that fuses low- and high-level image features with text embeddings for richer multi-modal representations. We evaluated our model on the M3D dataset, which includes radiology reports and VQA data for 120,084 3D medical images.
View Article and Find Full Text PDFFront Plant Sci
August 2025
College of Information and Electrical Engineering, Heilongjiang Bayi Agricultural University, Daqing, China.
Deep learning models for rice pest detection often face performance degradation in real-world field environments due to complex backgrounds and limited computational resources. Existing approaches suffer from two critical limitations: (1) inadequate feature representation under occlusion and scale variations, and (2) excessive computational costs for edge deployment. To overcome these limitations, this paper introduces GhostConv+CA-YOLOv8n, a lightweight object detection framework was proposed, which incorporates several innovative features: GhostConv replaces standard convolutional operations with computationally efficient ghost modules in the YOLOv8n's backbone structure, reducing parameters by 40,458 while maintaining feature richness; a Context Aggregation (CA) module is applied after the large and medium-sized feature maps were output by the YOLOv8n's neck structure.
View Article and Find Full Text PDFACS Appl Mater Interfaces
August 2025
Institute of Medical Technology, Peking University Health Science Center, Peking University, 38 Xueyuan Road, Haidian District, Beijing 100191, China.
Immunogenic cell death (ICD) induced in cancer chemotherapy, radiotherapy, and photodynamic therapy can facilitate the maturation of dendritic cells (DCs) and the activation, proliferation, and tumor infiltration of cytotoxic T lymphocytes, which may synergize with immune checkpoint blockade (ICB) therapy to improve therapeutic outcomes. Herein, we report a novel ICD inducer of TCS-ELP(HI), in which a multifunctional biologic of trichosanthin (TCS) is genetically fused to a thermo-pH-sensitive elastin-like polypeptide (ELP(HI)). This fusion offers a thermo-pH-sensitive property to TCS, leading to not only the formation of a sustained-released depot of TCS-ELP(HI) upon intratumoral injection but also the enhanced tumor cell uptake and lysosomal escape of TCS-ELP(HI) as compared to free TCS.
View Article and Find Full Text PDF