Natural product synthesis : nature.com subject feedshttps://www.nature.com/subjects/natural-product-synthesis.atom2024-03-28T12:20:32+00:00Enantioselective total synthesis of (‒)-lucidumone enabled by tandem prins cyclization/cycloetherification sequencehttps://www.nature.com/articles/s41467-024-46896-32024-03-26T00:00:00+00:002024-03-26T00:00:00+00:00Xian-Zhang Liao et al.Targeted sampling of natural product space to identify bioactive natural product-like polyketide macrolideshttps://www.nature.com/articles/s41467-024-46721-x2024-03-21T00:00:00+00:002024-03-21T00:00:00+00:00Darryl M. Wilson et al.Biosynthesis of the highly oxygenated tetracyclic core skeleton of Taxolhttps://www.nature.com/articles/s41467-024-46583-32024-03-15T00:00:00+00:002024-03-15T00:00:00+00:00Chengshuai Yang et al.Author Correction: Catalytic enantioselective reductive alkynylation of amides enables one-pot syntheses of pyrrolidine, piperidine and indolizidine alkaloidshttps://www.nature.com/articles/s41467-024-46252-52024-02-28T00:00:00+00:002024-02-28T00:00:00+00:00Fang-Fang Xu et al.Chemoenzymatic total synthesis of sorbicillactone Ahttps://www.nature.com/articles/s42004-024-01126-12024-02-24T00:00:00+00:002024-02-24T00:00:00+00:00Jonas I. Müller et al.Reconstitution of early paclitaxel biosynthetic networkhttps://www.nature.com/articles/s41467-024-45574-82024-02-15T00:00:00+00:002024-02-15T00:00:00+00:00Jack Chun-Ting Liu et al.Collective total synthesis of stereoisomeric yohimbine alkaloidshttps://www.nature.com/articles/s41467-024-45140-22024-01-31T00:00:00+00:002024-01-31T00:00:00+00:00Meiyi Tang et al.Elucidation of unusual biosynthesis and DnaN-targeting mode of action of potent anti-tuberculosis antibiotics Mycoplanecinshttps://www.nature.com/articles/s41467-024-44953-52024-01-26T00:00:00+00:002024-01-26T00:00:00+00:00Chengzhang Fu et al.Synthesis and biological evaluation of nectriatide derivatives, potentiators of amphotericin B activityhttps://www.nature.com/articles/s41429-023-00700-42024-01-24T00:00:00+00:002024-01-24T00:00:00+00:00Kenichiro Nagai et al.Total syntheses of Tetrodotoxin and 9-epiTetrodotoxinhttps://www.nature.com/articles/s41467-024-45037-02024-01-23T00:00:00+00:002024-01-23T00:00:00+00:00Peihao Chen et al.Biomimetic alkaloid synthesishttps://www.nature.com/articles/s44160-023-00475-42024-01-05T00:00:00+00:002024-01-05T00:00:00+00:00Peter W. SeavillChemical synthesis as a discovery platform in immunosuppression and determination of mode of actionhttps://www.nature.com/articles/s44160-023-00423-22024-01-04T00:00:00+00:002024-01-04T00:00:00+00:00Manuel Schupp et al.Discovery from Hypericum elatoides and synthesis of hyperelanitriles as α-aminopropionitrile-containing polycyclic polyprenylated acylphloroglucinolshttps://www.nature.com/articles/s42004-023-01091-12024-01-02T00:00:00+00:002024-01-02T00:00:00+00:00Jin-Yan Xie et al.C5 methylation confers accessibility, stability and selectivity to picrotoxininhttps://www.nature.com/articles/s41467-023-44030-32023-12-14T00:00:00+00:002023-12-14T00:00:00+00:00Guanghu Tong et al.A naturally occurring polyacetylene isolated from carrots promotes health and delays signatures of aginghttps://www.nature.com/articles/s41467-023-43672-72023-12-08T00:00:00+00:002023-12-08T00:00:00+00:00Carolin Thomas et al.Discovery of type II polyketide synthase-like enzymes for the biosynthesis of cispentacinhttps://www.nature.com/articles/s41467-023-43731-z2023-12-06T00:00:00+00:002023-12-06T00:00:00+00:00Genki Hibi et al.Publisher Correction: Synthesis of branched arabinogalactans up to a 140-mer from Panax notoginseng and their anti-pancreatic-cancer activityhttps://www.nature.com/articles/s44160-023-00459-42023-11-24T00:00:00+00:002023-11-24T00:00:00+00:00Xianjin Qin et al.Computational analysis and experimental verification of donor–acceptor behaviour of berberine, and its co-oligomers and co-polymers with ethylenedıoxythıophenehttps://www.nature.com/articles/s41598-023-47541-72023-11-18T00:00:00+00:002023-11-18T00:00:00+00:00R. M. Gamini Rajapakse et al.Computational prediction of complex cationic rearrangement outcomeshttps://www.nature.com/articles/s41586-023-06854-32023-11-15T00:00:00+00:002023-11-15T00:00:00+00:00Tomasz Klucznik et al.Antiviral potency of lupane and oleanane alkynyl-derivatives against human cytomegalovirus and papillomavirushttps://www.nature.com/articles/s41429-023-00672-52023-11-07T00:00:00+00:002023-11-07T00:00:00+00:00Elmira F. Khusnutdinova et al.Synthesis of branched arabinogalactans up to a 140-mer from Panax notoginseng and their anti-pancreatic-cancer activityhttps://www.nature.com/articles/s44160-023-00428-x2023-11-02T00:00:00+00:002023-11-02T00:00:00+00:00Xianjin Qin et al.Synthesis of tertiary alkylphosphonate oligonucleotides through light-driven radical-polar crossover reactionshttps://www.nature.com/articles/s41467-023-42639-y2023-10-31T00:00:00+00:002023-10-31T00:00:00+00:00Kenji Ota et al.Cu-catalyzed asymmetric regiodivergent electrosynthesis and its application in the enantioselective total synthesis of (-)-fumimycinhttps://www.nature.com/articles/s41467-023-42603-w2023-10-24T00:00:00+00:002023-10-24T00:00:00+00:00Tian Xie et al.Synergistic performance of a new bimetallic complex supported on magnetic nanoparticles for Sonogashira and C–N coupling reactionshttps://www.nature.com/articles/s41598-023-44168-62023-10-24T00:00:00+00:002023-10-24T00:00:00+00:00Fatemeh Nasseri et al.Triepoxide formation by a flavin-dependent monooxygenase in monensin biosynthesishttps://www.nature.com/articles/s41467-023-41889-02023-10-07T00:00:00+00:002023-10-07T00:00:00+00:00Qian Wang et al.Catalytic enantioselective reductive alkynylation of amides enables one-pot syntheses of pyrrolidine, piperidine and indolizidine alkaloidshttps://www.nature.com/articles/s41467-023-41846-x2023-10-06T00:00:00+00:002023-10-06T00:00:00+00:00Fang-Fang Xu et al.Author Correction: Synthesis of portimines reveals the basis of their anti-cancer activityhttps://www.nature.com/articles/s41586-023-06699-w2023-10-05T00:00:00+00:002023-10-05T00:00:00+00:00Junchen Tang et al.Optimizing acid overproductionhttps://www.nature.com/articles/s41589-023-01442-y2023-09-25T00:00:00+00:002023-09-25T00:00:00+00:00Russell JohnsonAuthor Correction: Chemoenzymatic approaches for exploring structure–activity relationship studies of bioactive natural productshttps://www.nature.com/articles/s44160-023-00421-42023-09-25T00:00:00+00:002023-09-25T00:00:00+00:00Fuzhuo Li et al.Generation of potent antibacterial compounds through enzymatic and chemical modifications of the trans-δ-viniferin scaffoldhttps://www.nature.com/articles/s41598-023-43000-52023-09-25T00:00:00+00:002023-09-25T00:00:00+00:00Robin Huber et al.