Divergent access to 5,6,7-perifused cycles

[1]  Baosheng Li,et al.  Cascade 8π Electrocyclization/Benzannulation to Access Highly Substituted Phenylpyridines. , 2021, Organic letters.

[2]  Tao Wang,et al.  Divergent Synthesis of Highly Substituted Pyridines and Benzenes from Dienals, Alkynes, and Sulfonyl Azides. , 2021, Organic letters.

[3]  Baosheng Li,et al.  Copper and Rhodium Relay Catalysis for Selective Access to cis-2,3-Dihydroazepines. , 2021, Organic letters.

[4]  Magnus J. Johansson,et al.  Late-stage C–H functionalization offers new opportunities in drug discovery , 2021, Nature Reviews Chemistry.

[5]  M. Barker,et al.  Investigating the effects of the core nitrogen atom configuration on the thermodynamic solubility of 6,5-bicyclic heterocycles. , 2020, Bioorganic & medicinal chemistry letters.

[6]  N. Shibata,et al.  Modular Synthesis of Medium-Sized Fluorinated and Nonfluorinated Heterocyclic Lactones by Sequential CN-Bond-Cleaving Ring Expansion under Pd Catalysis , 2020 .

[7]  Feng-Lin Hong,et al.  Transition Metal-Catalyzed Tandem Reactions of Ynamides for Divergent N-Heterocycle Synthesis. , 2020, Accounts of chemical research.

[8]  Y. Cohen,et al.  Creating Stereocenters within Acyclic Systems by C-C Bond Cleavage of Cyclopropanes. , 2020, Chemical reviews.

[9]  Tongyu Xu,et al.  Synthesis of Indolizine Derivatives Triggered by the Oxidative Addition of Aroyl Chloride to Pd(0) Complex. , 2020, The Journal of organic chemistry.

[10]  D. Jwa,et al.  Recent Organic Transformations with Silver Carbonate as a Key External Base and Oxidant , 2019 .

[11]  Michael Moir,et al.  An overview of late-stage functionalization in today’s drug discovery , 2019, Expert opinion on drug discovery.

[12]  Xinhai Zhu,et al.  Copper-Catalyzed Cascade Cyclization of Indolyl Homopropargyl Amides: Stereospecific Construction of Bridged Aza-[n.2.1] Skeletons. , 2019, Angewandte Chemie.

[13]  Huiwei Bao,et al.  Antitussive and Anti-inflammatory Dual-active Agents Developed from Natural Product Lead Compound 1-Methylhydantoin , 2019, Molecules.

[14]  Jasper Biemolt,et al.  Advances in Palladium-Catalyzed Cascade Cyclizations , 2018, Advanced Synthesis & Catalysis.

[15]  Kai Chen,et al.  Transition-Metal-Catalyzed Intramolecular Nucleophilic Addition of Carbonyl Groups to Alkynes , 2018, Chem.

[16]  Huanfeng Jiang,et al.  CuCl/Et3N-Catalyzed Synthesis of Indanone-Fused 2-Methylene Pyrrolidines from Enynals and Propargylamines. , 2017, Organic letters.

[17]  D. Back,et al.  Copper‐Catalyzed Carbon‐Nitrogen/Carbon‐Selenium Bonds Formation: Synthesis of 2‐(Organochalcogenyl)‐indolizines , 2017 .

[18]  Jimin Yang,et al.  Catalytic B-H Bond Insertion Reactions Using Alkynes as Carbene Precursors. , 2017, Journal of the American Chemical Society.

[19]  N. Wang,et al.  Radical aryl migration enables diversity-oriented synthesis of structurally diverse medium/macro- or bridged-rings , 2016, Nature Communications.

[20]  Reema Abu Khalaf,et al.  Exploring Natural Products as a Source for Antidiabetic Lead Compounds and Possible Lead Optimization. , 2016, Current topics in medicinal chemistry.

[21]  Petra Schneider,et al.  Counting on natural products for drug design. , 2016, Nature chemistry.

[22]  Kyung Hwan Oh,et al.  Base-Controlled Cu-Catalyzed Tandem Cyclization/Alkynylation for the Synthesis of Indolizines. , 2016, Organic letters.

[23]  J. Yue,et al.  Mannolides A-C with an Intact Diterpenoid Skeleton Providing Insights on the Biosynthesis of Antitumor Cephalotaxus Troponoids. , 2016, Organic letters.

[24]  Shifa Zhu,et al.  Enynal/Enynone: A Safe and Practical Carbenoid Precursor , 2015 .

[25]  B. Shen.  A New Golden Age of Natural Products Drug Discovery , 2015, Cell.

[26]  H. Alper,et al.  Synthesis of Indolizine Derivatives by Pd-Catalyzed Oxidative Carbonylation. , 2015, Organic letters.

[27]  D. Newman,et al.  Natural products as leads to antitumor drugs , 2014, Phytochemistry Reviews.

[28]  V. Gevorgyan,et al.  Palladium-catalyzed carbonylative cyclization/arylation cascade for 2-aroylindolizine synthesis. , 2012, Organic letters.

[29]  A. Verma,et al.  Site-selective electrophilic cyclization and subsequent ring-opening: a synthetic route to pyrrolo[1,2-a]quinolines and indolizines. , 2012, The Journal of organic chemistry.

[30]  A. Corma,et al.  Gold-catalyzed carbon-heteroatom bond-forming reactions. , 2011, Chemical reviews.

[31]  V. Gevorgyan,et al.  Palladium-catalyzed intramolecular carbopalladation/cyclization cascade: access to polycyclic N-fused heterocycles. , 2010, Organic letters.

[32]  V. Gevorgyan,et al.  Two-component approach toward a fully substituted N-fused pyrrole ring. , 2010, Organic letters.

[33]  E. Nakamura,et al.  Efficient formation of ring structures utilizing multisite activation by indium catalysis. , 2008, Journal of the American Chemical Society.

[34]  Jian-hua Liu,et al.  Ainsliatrimers A and B, the first two guaianolide trimers from Ainsliaea fulvioides. , 2008, Organic letters.

[35]  R. Sarpong,et al.  Pt-catalyzed cyclization/migration of propargylic alcohols for the synthesis of 3(2H)-furanones, pyrrolones, indolizines, and indolizinones. , 2008, Tetrahedron.

[36]  V. Gevorgyan,et al.  Multisubstituted N-fused heterocycles via transition metal-catalyzed cycloisomerization protocols. , 2008, Tetrahedron.

[37]  Hao Zhang,et al.  Highly efficient synthesis of functionalized indolizines and indolizinones by copper-catalyzed cycloisomerizations of propargylic pyridines. , 2007, The Journal of organic chemistry.

[38]  V. Gevorgyan,et al.  Base- and ligand-free room-temperature synthesis of N-fused heteroaromatic compounds via the transition metal-catalyzed cycloisomerization protocol. , 2007, Organic letters.

[39]  R. Sarpong,et al.  Pt-catalyzed cyclization/1,2-migration for the synthesis of indolizines, pyrrolones, and indolizinones. , 2007, Organic letters.

[40]  Liming Zhang,et al.  Gold and platinum catalysis of enyne cycloisomerization , 2006 .

[41]  V. Gevorgyan,et al.  Gold-catalyzed 1,2-migration of silicon, tin, and germanium en route to C-2 substituted fused pyrrole-containing heterocycles. , 2006, Journal of the American Chemical Society.

[42]  L. Yet.  Metal-mediated synthesis of medium-sized rings. , 2000, Chemical reviews.

[43]  G. Molander.  Diverse Methods for Medium Ring Synthesis , 1998 .

[44]  M. Malacria.  Selective Preparation of Complex Polycyclic Molecules from Acyclic Precursors via Radical Mediated- or Transition Metal-Catalyzed Cascade Reactions. , 1996, Chemical reviews.

[45]  T. Hudlický,et al.  Use of cyclopropanes and their derivatives in organic synthesis , 1989 .

[46]  W. Flitsch,et al.  Beiträge zur Chemie der Cycl[4.3.2]azine , 1979 .

[47]  W. Flitsch,et al.  Zur Chemie der Cycl[4.3.2]azine , 1975 .

[48]  W. Flitsch,et al.  Cycl[4.3.2]azin‐4,5‐dicarbonsäure‐diäthylester , 1973 .

[49]  W. Sippl,et al.  Synthesis and Biological Investigation of Phenothiazine-Based Benzhydroxamic Acids as Selective Histone Deacetylase 6 Inhibitors. , 2019, Journal of medicinal chemistry.

[50]  R. Baker,et al.  Soldier defense secretions of the south american termites Cortaritermes Silvestri, Nasutitermes SP N.D and Nasutitermes Kemneri , 1982 .

[51]  Roald Hoffmann,et al.  Conservation of orbital symmetry , 1968 .

[52]  Roald Hoffmann,et al.  Stereochemistry of Electrocyclic Reactions (福井謙一とフロンティア軌導理論) -- (参考論文) , 1965 .