Toward Generalization of Iterative Small Molecule Synthesis.
暂无分享,去创建一个
[1] William H. Gerwick,et al. Retrospective analysis of natural products provides insights for future discovery trends , 2017, Proceedings of the National Academy of Sciences.
[2] M. Turner,et al. A General Protocol for the Polycondensation of Thienyl N-Methyliminodiacetic Acid Boronate Esters To Form High Molecular Weight Copolymers , 2016, Journal of the American Chemical Society.
[3] F. West,et al. New efficient iterative approaches to polycyclic ethers. , 2002, Chemistry.
[4] R. Noyori,et al. Sulfonyl-stabilized oxiranyllithium-based approach to polycyclic ethers. Convergent synthesis of the ABCDEF-ring system of yessotoxin and adriatoxin. , 2003, The Journal of organic chemistry.
[5] J. Ellman,et al. Asymmetric Rh(I)-catalyzed addition of MIDA boronates to N-tert-butanesulfinyl aldimines: development and comparison to trifluoroborates. , 2010, The Journal of organic chemistry.
[6] V. Aggarwal,et al. Short Enantioselective Total Synthesis of Tatanan A and 3‐epi‐Tatanan A Using Assembly‐Line Synthesis , 2016, Angewandte Chemie.
[7] Dima Kozakov,et al. How Proteins Bind Macrocycles , 2014, Nature chemical biology.
[8] Thomas H Segall-Shapiro,et al. Creation of a Bacterial Cell Controlled by a Chemically Synthesized Genome , 2010, Science.
[9] Carolyn C. Cooper,et al. The Portsmouth System of Manufacture , 1984 .
[10] Junji Kido,et al. Solution-processed multilayer small-molecule light-emitting devices with high-efficiency white-light emission , 2014, Nature Communications.
[11] D. Newman,et al. Natural Products as Sources of New Drugs from 1981 to 2014. , 2016, Journal of natural products.
[12] G. Poda,et al. Condensation-Driven Assembly of Boron-Containing Bis(Heteroaryl) Motifs Using a Linchpin Approach. , 2015, Organic letters.
[13] A. Davies,et al. From the American System to Mass Production, 1800-1932: The Development of Manufacturing Technology in the United States. , 1985 .
[14] Julien C. Vantourout,et al. One-Pot Homologation of Boronic Acids: A Platform for Diversity-Oriented Synthesis. , 2015, Organic letters.
[15] S. Kent. Total chemical synthesis of proteins. , 2009, Chemical Society reviews.
[16] P. Phansavath,et al. Heck coupling using a vinyliodo-MIDA boronate: an efficient and modular access to polyene frameworks. , 2015, Organic letters.
[17] R. Mart,et al. Azobenzene photocontrol of peptides and proteins. , 2016, Chemical communications.
[18] Gregory W. Kauffman,et al. Discovery of the Potent and Selective M1 PAM-Agonist N-[(3R,4S)-3-Hydroxytetrahydro-2H-pyran-4-yl]-5-methyl-4-[4-(1,3-thiazol-4-yl)benzyl]pyridine-2-carboxamide (PF-06767832): Evaluation of Efficacy and Cholinergic Side Effects. , 2016, Journal of medicinal chemistry.
[19] Mark Peplow,et al. Organic synthesis: The robo-chemist , 2014, Nature.
[20] W. Wernsdorfer,et al. Electrically driven nuclear spin resonance in single-molecule magnets , 2014, Science.
[21] M. Bols,et al. Synthesis of L-Hexoses. , 2015, Chemical reviews.
[22] B. Cravatt,et al. Facile synthesis of borofragments and their evaluation in activity-based protein profiling. , 2015, Chemical communications.
[23] H. Brown,et al. Chiral synthesis via organoboranes. 7. Diastereoselective and enantioselective synthesis of erythro- and threo-.beta.-methylhomoallyl alcohols via enantiomeric (Z)- and (E)-crotylboranes. , 1986, Journal of the American Chemical Society.
[24] H. Brown,et al. Enantiomeric (Z)- and (E)-Crotyldiisopinocampheylboranes. Synthesis in High Optical Purity of All Four Possible Stereoisomers of β-Methylhomoallyl Alcohols. , 2002 .
[25] P. Le Pape,et al. Design, synthesis and biological evaluation of novel 4-alkapolyenylpyrrolo[1,2-a]quinoxalines as antileishmanial agents--part III. , 2014, European journal of medicinal chemistry.
[26] A. Yudin,et al. Amphoteric α-Boryl Aldehyde Linchpins in the Synthesis of Heterocycles , 2015 .
[27] Erin E. Carlson,et al. Progress and prospects for small-molecule probes of bacterial imaging. , 2016, Nature chemical biology.
[28] Ben W. Glasspoole,et al. Cross coupling reactions of chiral secondary organoboronic esters with retention of configuration. , 2009, Journal of the American Chemical Society.
[29] Jeffrey S. Moore,et al. Geometrically-Controlled and Site-Specifically-Functionalized Phenylacetylene Macrocycles , 1994 .
[30] D. Caro,et al. TTF[Ni(dmit)2]2: From single-crystals to thin layers, nanowires, and nanoparticles , 2016 .
[31] J. Ellman,et al. Total synthesis of (-)-aurantioclavine. , 2010, Organic letters.
[32] Frank F. Bier,et al. Miniaturization for Point-of-Care Analysis: Platform Technology for Almost Every Biomedical Assay , 2012, EJIFCC.
[33] Eric M. Woerly,et al. A General Solution for the 2-Pyridyl Problem , 2012, Angewandte Chemie.
[34] H. Brown,et al. Enantiomeric Z- and E-crotyldiisopinocampheylboranes. Synthesis in high optical purity of all four possible stereoisomers of .beta.-methylhomoallyl alcohols , 1986 .
[35] Rongcai Huang,et al. Stereoretentive Pd-catalysed Stille cross-coupling reactions of secondary alkyl azastannatranes and aryl halides , 2013, Nature Chemistry.
[36] R. B. Merrifield. Automated synthesis of peptides. , 1965, Science.
[37] S. Masamune,et al. Total Synthesis of the L-Hexoses , 1983, Science.
[38] A. Yudin,et al. Amphoteric α-boryl aldehydes. , 2011, Journal of the American Chemical Society.
[39] A. Echavarren,et al. Nonacene Generated by On-Surface Dehydrogenation. , 2017, ACS nano.
[40] Carl Schubert,et al. Innovations in 3D printing: a 3D overview from optics to organs , 2013, British Journal of Ophthalmology.
[41] B. Breit,et al. Iterative synthesis of (oligo)deoxypropionates via zinc-catalyzed enantiospecific sp3-sp3 cross-coupling. , 2009, Organic letters.
[42] Brice E. Uno,et al. C2'-OH of amphotericin B plays an important role in binding the primary sterol of human cells but not yeast cells. , 2013, Journal of the American Chemical Society.
[43] Francesco Falciani,et al. DNA Microarrays: a Powerful Genomic Tool for Biomedical and Clinical Research , 2007, Molecular medicine.
[44] L. Meijer,et al. Discovery of the First Potent and Selective Inhibitors of Human dCTP Pyrophosphatase 1. , 2016, Journal of medicinal chemistry.
[45] S. Lindquist,et al. Non-toxic antimicrobials that evade drug resistance , 2015, Nature chemical biology.
[46] Peter H. Seeberger,et al. Automated synthesis of oligosaccharides as a basis for drug discovery , 2005, Nature Reviews Drug Discovery.
[47] Chun-Young Lee,et al. Synthesis of Optically Pure 3,3'-Disubstituted-1,1'-Bi-6-Methoxy-2-Phenol (BIPhOL) Derivatives via Diastereomeric Resolution. , 2016, The Journal of organic chemistry.
[48] 中西 香爾,et al. Comprehensive natural products chemistry , 1999 .
[49] Charles L. Wilkins,et al. Phenylacetylene Dendrimers by the Divergent, Convergent, and Double-Stage Convergent Methods , 1994 .
[50] D. Hall,et al. Enantioselective preparation and chemoselective cross-coupling of 1,1-diboron compounds. , 2011, Nature chemistry.
[51] M. Crimmins,et al. Titanium enolates of thiazolidinethione chiral auxiliaries: versatile tools for asymmetric aldol additions. , 2000, Organic letters.
[52] Gerlach,et al. A Combinatorial Approach to Polyketide-Type Libraries by Iterative Asymmetric Aldol Reactions Performed on Solid Support We thank the European Commission (TMR Network ERB-FMR XCT 96-0011 and IHP Network HPRN-CT-2000-00014), EPSRC, Pfizer, and Merck for support. , 2000, Angewandte Chemie.
[53] Ling Li,et al. Stereospecific Pd-Catalyzed Cross-Coupling Reactions of Secondary Alkylboron Nucleophiles and Aryl Chlorides , 2014, Journal of the American Chemical Society.
[54] Jeffrey S. Moore,et al. Improvements in the Synthesis of Phenylacetylene Monodendrons Including a Solid-Phase Convergent Method , 1995 .
[55] David A. Nicewicz,et al. Organic Photoredox Catalysis. , 2016, Chemical reviews.
[56] F. Toste,et al. Tandem Cycloisomerization/Suzuki Coupling of Arylethynyl MIDA Boronates. , 2011, Tetrahedron.
[57] Christopher J Chang,et al. Reaction-based small-molecule fluorescent probes for chemoselective bioimaging. , 2012, Nature chemistry.
[58] A. Myers,et al. Asymmetric Synthesis of 1,3-Dialkyl-Substituted Carbon Chains of any Stereochemical Configuration by an Iterable Process , 1997 .
[59] Andreas P Häring,et al. Versatile process for the stereodiverse construction of 1,3-polyols: iterative chain elongation with chiral building blocks. , 2016, Chemical communications.
[60] Kenneth L. Alder,et al. Innovation and Amnesia: Engineering Rationality and the Fate of Interchangeable Parts Manufacturing in France , 1997, Technology and Culture.
[61] M. Krische,et al. Total Synthesis of Swinholide A: An Exposition in Hydrogen-Mediated C-C Bond Formation. , 2016, Journal of the American Chemical Society.
[62] T. Hansen,et al. Synthesis of methyl (5Z,8Z,10E,12E,14Z)-eicosapentaenoate , 2011 .
[63] Nicholas C. Davy,et al. Contorted Hexabenzocoronenes with Extended Heterocyclic Moieties Improve Visible-Light Absorption and Performance in Organic Solar Cells , 2016 .
[64] M. Suginome,et al. Stereospecific Suzuki-Miyaura coupling of chiral α-(acylamino)benzylboronic esters with inversion of configuration. , 2010, Journal of the American Chemical Society.
[65] Steven V Ley,et al. Flow chemistry syntheses of natural products. , 2013, Chemical Society reviews.
[66] Martin D. Burke,et al. Synthesis of many different types of organic small molecules using one automated process , 2015, Science.
[67] Frank Schuhmacher,et al. Automated glycan assembly using the Glyconeer 2.1 synthesizer , 2017, Proceedings of the National Academy of Sciences.
[68] Alexander G. Godfrey,et al. A remote-controlled adaptive medchem lab: an innovative approach to enable drug discovery in the 21st Century. , 2013, Drug discovery today.
[69] M. Johnston,et al. Procyanidin oligomers. A new method for 4→8 interflavan bond formation using C8-boronic acids and iterative oligomer synthesis through a boron-protection strategy , 2012 .
[70] A. Yudin,et al. Synthesis of Previously Inaccessible Borylated Heterocycle Motifs Using Novel Boron-Containing Amphoteric Molecules. , 2015, Angewandte Chemie.
[71] B. W. King,et al. Asymmetric aldol additions: use of titanium tetrachloride and (-)-sparteine for the soft enolization of N-acyl oxazolidinones, oxazolidinethiones, and thiazolidinethiones. , 2001, The Journal of organic chemistry.
[72] M. Krische,et al. Total synthesis of (+)-roxaticin via C-C bond forming transfer hydrogenation: a departure from stoichiometric chiral reagents, auxiliaries, and premetalated nucleophiles in polyketide construction. , 2010, Journal of the American Chemical Society.
[73] Jeffrey S. Moore,et al. Nanoarchitectures. 1. Controlled synthesis of phenylacetylene sequences , 1992 .
[74] Benjamin L. Miller,et al. Synthesis at the molecular frontier , 2009, Nature.
[75] K. Nicolaou,et al. Retrosynthetic and synthetic chemistry on amphotericin B. Synthesis of C(1)–C(20) and C(21)–C(38) fragments and construction of the 38-membered macrocycle , 1986 .
[76] Bethany C Gross,et al. Evaluation of 3D printing and its potential impact on biotechnology and the chemical sciences. , 2014, Analytical chemistry.
[77] L. Hamann,et al. One-pot C-N/C-C cross-coupling of methyliminodiacetic acid boronyl arenes enabled by protective enolization. , 2012, Organic letters.
[78] M. Caruthers,et al. Gene synthesis machines: DNA chemistry and its uses. , 1985, Science.
[79] Kumar Yelamarthi,et al. An Application-Driven Modular IoT Architecture , 2017, Wirel. Commun. Mob. Comput..
[80] R. Iyer. 7.05 – Oligonucleotide Synthesis , 1999 .
[81] Carliss Y. Baldwin,et al. Managing in an age of modularity. , 1997, Harvard business review.
[82] Eric M. Woerly,et al. Synthesis of most polyene natural product motifs using just twelve building blocks and one coupling reaction , 2014, Nature chemistry.
[83] M. Carda,et al. On the structure of passifloricin A: asymmetric synthesis of the delta-lactones of (2Z,5S,7R,9S,11S)- and (2Z,5R,7R,9S,11S)tetrahydroxyhexacos-2-enoic acid. , 2003, Organic letters.
[84] S. Buchwald,et al. Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions employing dialkylbiaryl phosphine ligands. , 2008, Accounts of chemical research.
[85] M. Burke,et al. Simple, efficient, and modular syntheses of polyene natural products via iterative cross-coupling. , 2008, Journal of the American Chemical Society.
[86] C. Crudden,et al. Iterative protecting group-free cross-coupling leading to chiral multiply arylated structures , 2016, Nature Communications.
[87] S. Ishibashi,et al. A single-component molecular superconductor. , 2014, Journal of the American Chemical Society.
[88] V. Aggarwal,et al. Synthesis of enantioenriched tertiary boronic esters from secondary allylic carbamates. Application to the synthesis of C30 botryococcene. , 2012, Journal of the American Chemical Society.
[89] Lee Joon Kim,et al. Concise, diastereoconvergent synthesis of endiandric-type tetracycles by iterative cross coupling , 2016 .
[90] J. Pascual,et al. Protection of excited spin states by a superconducting energy gap , 2013, Nature Physics.
[91] A. Minnaard,et al. Total synthesis of sulfolipid-1. , 2014, Chemical communications.
[92] Nancy R. Sottos,et al. Biasing reaction pathways with mechanical force , 2007, Nature.
[93] A. Goffeau,et al. Outwitting Multidrug Resistance to Antifungals , 2008, Science.
[94] J. Hartwig. Organotransition Metal Chemistry: From Bonding to Catalysis , 2009 .
[95] Daniel S. Palacios,et al. Amphotericin primarily kills yeast by simply binding ergosterol , 2012, Proceedings of the National Academy of Sciences.
[96] Matthew Burns,et al. Assembly-line synthesis of organic molecules with tailored shapes , 2014, Nature.
[97] B. Wrackmeyer,et al. New bicyclic organylboronic esters derived from iminodiacetic acids , 1986 .
[98] Sarah E Bohndiek,et al. Contrast agents for molecular photoacoustic imaging , 2016, Nature Methods.
[99] J. Kath,et al. Daphniphyllum alkaloids. 12. A proposed biosynthesis of the pentacylic skeleton. proto-Daphniphylline , 1992 .
[100] K. Nicolaou,et al. Total synthesis of amphoteronolide B and amphotericin B. 2. Total synthesis of amphoteronolide B , 1988 .
[101] T. M. Anderson,et al. A Simple and General Platform for Generating Stereochemically Complex Polyene Frameworks by Iterative Cross-Coupling , 2010, Angewandte Chemie.
[102] John E Anthony,et al. The larger acenes: versatile organic semiconductors. , 2008, Angewandte Chemie.
[103] J. Spencer,et al. Regioselective routes to orthogonally-substituted aromatic MIDA boronates. , 2016, Organic & biomolecular chemistry.
[104] S. H. Kim,et al. Stereoselective total synthesis of (-)-borrelidin. , 2004, Angewandte Chemie.
[105] Qingjiang Li,et al. Oxidative Difunctionalization of Alkenyl MIDA Boronates: A Versatile Platform for Halogenated and Trifluoromethylated α-Boryl Ketones. , 2016, Angewandte Chemie.
[106] Kyoung Sun Moon,et al. Structural Developments in Tall Buildings: Current Trends and Future Prospects , 2007 .
[107] B. Feringa,et al. Iterative strategies for the synthesis of deoxypropionates. , 2010, Chemical communications.
[108] S. Cobb,et al. Synthesis of biaryl-linked cyclic peptoids. , 2017 .
[109] Jiajie Feng,et al. Enantioselective Alcohol C-H Functionalization for Polyketide Construction: Unlocking Redox-Economy and Site-Selectivity for Ideal Chemical Synthesis. , 2016, Journal of the American Chemical Society.
[110] M. Krische,et al. Total synthesis of 6-deoxyerythronolide B via C-C bond-forming transfer hydrogenation. , 2013, Journal of the American Chemical Society.
[111] E. Gouaux,et al. Glycine receptor mechanism elucidated by electron cryo-microscopy , 2015, Nature.
[112] Bruno G. Nicolau,et al. Restored iron transport by a small molecule promotes absorption and hemoglobinization in animals , 2017, Science.
[113] M. Coltheart,et al. Modularity of music processing , 2003, Nature Neuroscience.
[114] Victor Snieckus,et al. Palladium-catalyzed cross-coupling: a historical contextual perspective to the 2010 Nobel Prize. , 2012, Angewandte Chemie.
[115] H. Bettinger,et al. Photogeneration of octacene and nonacene. , 2010, Angewandte Chemie.
[116] Chris Twelves,et al. Eribulin monotherapy versus treatment of physician's choice in patients with metastatic breast cancer (EMBRACE): a phase 3 open-label randomised study , 2011, The Lancet.
[117] Shogo Arakawa,et al. Total Synthesis of Gymnocin-A. , 2015, Journal of the American Chemical Society.
[118] H. G. Khorana. Total synthesis of a gene , 2012, Die Naturwissenschaften.
[119] M. Garcia‐Garibay,et al. Phosphine-Mediated Iterative Arene Homologation Using Allenes. , 2015, Journal of the American Chemical Society.
[120] A. Yudin,et al. Boron-containing enamine and enamide linchpins in the synthesis of nitrogen heterocycles. , 2014, Journal of the American Chemical Society.
[121] J. Cossy,et al. Synthesis of the Acyclic Carbon Skeleton of Filipin III. , 2016, The Journal of organic chemistry.
[122] T. Hoffmann,et al. Peptide therapeutics: current status and future directions. , 2015, Drug discovery today.
[123] Petra Schneider,et al. Counting on natural products for drug design. , 2016, Nature chemistry.
[124] A. Echavarren,et al. Strategies for the Synthesis of Higher Acenes , 2016, European journal of organic chemistry.
[125] J. Sperry,et al. Extending the Utility of the Bartoli Indolization: Synthesis of Marinoquinolines C and E , 2013, Synlett.
[126] Hao Li,et al. Photoacoustic Probes for Ratiometric Imaging of Copper(II). , 2015, Journal of the American Chemical Society.
[127] E. Negishi,et al. A novel, highly selective, and general methodology for the synthesis of 1,5-diene-containing oligoisoprenoids of all possible geometrical combinations exemplified by an iterative and convergent synthesis of coenzyme Q(10). , 2002, Organic letters.
[128] M. Burke,et al. A general solution for unstable boronic acids: slow-release cross-coupling from air-stable MIDA boronates. , 2009, Journal of the American Chemical Society.
[129] Jeffrey S. Moore. Shape-Persistent Molecular Architectures of Nanoscale Dimension , 1997 .
[130] B. Feringa,et al. Catalytic asymmetric synthesis of phthioceranic acid, a heptamethyl-branched acid from Mycobacterium tuberculosis. , 2007, Organic letters.
[131] G. Molander,et al. Stereospecific cross-coupling of secondary organotrifluoroborates: potassium 1-(benzyloxy)alkyltrifluoroborates. , 2012, Journal of the American Chemical Society.
[132] Heidi Ledford,et al. Complex synthesis yields breast-cancer therapy , 2010, Nature.
[133] S. Laschat,et al. Strategies for the Synthesis of Deoxypropionates , 2016, Synthesis.
[134] J. N. Johnston,et al. A case study in biomimetic total synthesis: polyolefin carbocyclizations to terpenes and steroids. , 2005, Chemical reviews.
[135] J. M. Takacs,et al. Enantioselective γ-borylation of unsaturated amides and stereoretentive Suzuki–Miyaura cross-coupling† †Electronic supplementary information (ESI) available: Catalyst optimization data; experimental procedures; compound characterization data; spectra. See DOI: 10.1039/c7sc01093a , 2017, Chemical science.
[136] N. Harada,et al. Light-driven monodirectional molecular rotor , 2022 .
[137] A. Whiting,et al. Regioisomeric and Substituent Effects upon the Outcome of the Reaction of 1-Borodienes with Nitrosoarene Compounds. , 2015, The Journal of organic chemistry.
[138] Stephen P. Thomas,et al. Homologation and alkylation of boronic esters and boranes by 1,2-metallate rearrangement of boronate complexes. , 2009, Chemical record.
[139] Matthew Burns,et al. Toward ideality: the synthesis of (+)-kalkitoxin and (+)-hydroxyphthioceranic acid by assembly-line synthesis. , 2015, Journal of the American Chemical Society.
[140] Chao-yuan Wang,et al. Stereospecific Palladium-Catalyzed Acylation of Enantioenriched Alkylcarbastannatranes: A General Alternative to Asymmetric Enolate Reactions. , 2017, Angewandte Chemie.
[141] Alan H. Cherney,et al. Stereoretentive Suzuki-Miyaura coupling of haloallenes enables fully stereocontrolled access to (-)-peridinin. , 2010, Journal of the American Chemical Society.
[142] A. Campbell,et al. Synthesis of 2-BMIDA 6,5-bicyclic heterocycles by Cu(i)/Pd(0)/Cu(ii) cascade catalysis of 2-iodoaniline/phenols. , 2016, Chemical communications.
[143] M. Burke,et al. A simple and modular strategy for small molecule synthesis: iterative Suzuki-Miyaura coupling of B-protected haloboronic acid building blocks. , 2007, Journal of the American Chemical Society.
[144] Luca Cera,et al. Iterative Synthesis of Oligo[n]rotaxanes in Excellent Yield. , 2016, Journal of the American Chemical Society.
[145] Mitchell T. Ong,et al. Force-induced activation of covalent bonds in mechanoresponsive polymeric materials , 2009, Nature.
[146] M. Suginome,et al. Synthesis of B-protected beta-styrylboronic acids via iridium-catalyzed hydroboration of alkynes with 1,8-naphthalenediaminatoborane leading to iterative synthesis of oligo(phenylenevinylene)s. , 2009, Organic letters.
[147] M. Suginome,et al. Boron-masking strategy for the selective synthesis of oligoarenes via iterative Suzuki-Miyaura coupling. , 2007, Journal of the American Chemical Society.
[148] V. Aggarwal,et al. Lithiation-borylation methodology and its application in synthesis. , 2014, Accounts of chemical research.
[149] S. Katsumura,et al. Stereocontrolled Synthesis of Paracentrone , 2016, Synlett.
[150] Davidr . Evans,et al. Diastereoselective aldol reactions using .beta.-keto imide derived enolates. A versatile approach to the assemblage of polypropionate systems , 1990 .
[151] H. Brown,et al. .beta.-Allyldiisopinocampheylborane: a remarkable reagent for the diastereoselective allylboration of .alpha.-substituted chiral aldehydes , 1987 .
[152] K. Palczewski,et al. Chemistry of the Retinoid (Visual) Cycle , 2013, Chemical reviews.
[153] A. Beck‐Sickinger,et al. Automated solid-phase peptide synthesis to obtain therapeutic peptides , 2014, Beilstein journal of organic chemistry.
[154] Yan Meng,et al. A generic architecture of modular embedded system for miniature mobile robots , 2008, 2008 IEEE/RSJ International Conference on Intelligent Robots and Systems.
[155] A. Schimmer,et al. α-Boryl isocyanides enable facile preparation of bioactive boropeptides. , 2013, Angewandte Chemie.
[156] Peter H. Seeberger,et al. Automated Solid-Phase Synthesis of Oligosaccharides , 2001, Science.
[157] C. Butts,et al. Synergy of synthesis, computation and NMR reveals correct baulamycin structures , 2017, Nature.
[158] M. Burke,et al. Multistep synthesis of complex boronic acids from simple MIDA boronates. , 2008, Journal of the American Chemical Society.
[159] S. Zard,et al. Radical Instability in Aid of Efficiency: A Powerful Route to Highly Functional MIDA Boronates. , 2015, Journal of the American Chemical Society.
[160] J. T. Njardarson,et al. Analysis of the structural diversity, substitution patterns, and frequency of nitrogen heterocycles among U.S. FDA approved pharmaceuticals. , 2014, Journal of medicinal chemistry.
[161] anastasia. khvorova,et al. The chemical evolution of oligonucleotide therapies of clinical utility , 2017, Nature Biotechnology.
[162] Susumu Kobayashi,et al. Concise total synthesis of (-)-myxalamide A. , 2012, Angewandte Chemie.
[163] Alexander G Cioffi,et al. Restored Physiology in Protein-Deficient Yeast by a Small Molecule Channel. , 2015, Journal of the American Chemical Society.
[164] M. Burke,et al. Pinene-Derived Iminodiacetic Acid (PIDA): A Powerful Ligand for Stereoselective Synthesis and Iterative Cross-Coupling of C(sp3) Boronate Building Blocks , 2011, Journal of the American Chemical Society.
[165] Ryan B. Wicker,et al. 3D Printing for the Rapid Prototyping of Structural Electronics , 2014, IEEE Access.
[166] Richard C. Rattenbury. A Legacy in Arms: American Firearm Manufacture, Design, and Artistry, 1800–1900 , 2014 .
[167] Ventola Cl. Medical Applications for 3D Printing: Current and Projected Uses. , 2014 .
[168] Y. Mori,et al. Total synthesis of gambierol by using oxiranyl anions. , 2010, Chemistry.
[169] A. Suzuki,et al. Construction of Iterative Tetrahydrofuran Ring Units and Total Synthesis of (+)-Goniocin. , 2016, Organic letters.
[170] P. Nielsen,et al. Increasing the Stability of DNA:RNA Duplexes by Introducing Stacking Phenyl-Substituted Pyrazole, Furan, and Triazole Moieties in the Major Groove. , 2015, The Journal of organic chemistry.
[171] David A. Hounshell,et al. From the American System to Mass Production 1800–1932: The Development of Manufacturing Technology in the United States by David A. Hounshell (review) , 2023 .
[172] J. V. Nelson,et al. Stereoselective aldol condensations via boron enolates , 1979 .
[173] P. Blumberg,et al. Evaluation of Chromane-Based Bryostatin Analogues Prepared via Hydrogen-Mediated C-C Bond Formation: Potency Does Not Confer Bryostatin-like Biology. , 2016, Journal of the American Chemical Society.
[174] Raghu Garud,et al. Managing in the modular age : architectures, networks, and organizations , 2002 .
[175] T. Hiyama,et al. A silicon-based approach to oligoarenes by iterative cross-coupling reactions of halogenated organo[(2-hydroxymethyl)phenyl]dimethylsilanes. , 2007, Journal of the American Chemical Society.
[176] S. Y. Wong,et al. On-demand continuous-flow production of pharmaceuticals in a compact, reconfigurable system , 2016, Science.
[177] A. Yudin,et al. Chemoselective palladium-catalyzed α-allylation of α-boryl aldehydes. , 2012, Organic & biomolecular chemistry.
[178] M. Turner,et al. Thienyl MIDA Boronate Esters as Highly Effective Monomers for Suzuki-Miyaura Polymerization Reactions , 2015 .
[179] G. Molander,et al. Stereospecific cross-coupling of secondary alkyl β-trifluoroboratoamides. , 2010, Journal of the American Chemical Society.
[180] R. Ruffo,et al. Quaterpyridine ligands for panchromatic Ru(II) dye sensitizers. , 2012, The Journal of organic chemistry.
[181] Ben W. Glasspoole,et al. Synthesis of enantiomerically enriched triarylmethanes by enantiospecific Suzuki-Miyaura cross-coupling reactions. , 2014, Journal of the American Chemical Society.
[182] Synthetic studies on borrelidin: enantioselective synthesis of the C1-C12 fragment. , 2003 .
[183] P. Brémond,et al. Total synthesis of halichondrin C. , 2012, Journal of the American Chemical Society.
[184] M. Crimmins,et al. Formal synthesis of 6-deoxyerythronolide B. , 2006, Organic letters.
[185] A. Kirschning,et al. Total synthesis of the antibiotic elansolid B1. , 2014, Organic letters.
[186] M. Suginome,et al. Inversion or retention? Effects of acidic additives on the stereochemical course in enantiospecific Suzuki-Miyaura coupling of α-(acetylamino)benzylboronic esters. , 2011, Journal of the American Chemical Society.
[187] Tim Lenoir,et al. The emergence and diffusion of DNA microarray technology , 2006, Journal of biomedical discovery and collaboration.
[188] Andrea M E Palazzolo,et al. The natural productome , 2017, Proceedings of the National Academy of Sciences.
[189] Mary M. Caruso,et al. Evaluation of ruthenium catalysts for ring-opening metathesis polymerization-based self-healing applications , 2008 .
[190] Jeffrey S. Moore,et al. Rapid Construction of Large‐size Phenylacetylene Dendrimers up to 12.5 Nanometers in Molecular Diameter , 1993 .
[191] J. L. Gleason,et al. Use of Pseudoephedrine as a Practical Chiral Auxiliary for Asymmetric Synthesis , 1994 .
[192] S. Goldup,et al. The active template approach to interlocked molecules , 2017 .
[193] T. Swager,et al. Mechanochemical Synthesis of Extended Iptycenes. , 2016, Journal of the American Chemical Society.
[194] M. Krische,et al. Polyketide construction via hydrohydroxyalkylation and related alcohol C-H functionalizations: reinventing the chemistry of carbonyl addition. , 2014, Natural product reports.
[195] M. Burke,et al. Total Synthesis of Synechoxanthin through Iterative Cross-Coupling** , 2011, Angewandte Chemie.
[196] J. Elkins,et al. Oxalyl Boronates Enable Modular Synthesis of Bioactive Imidazoles. , 2017, Angewandte Chemie.
[197] K. Houk,et al. MIDA boronates are hydrolysed fast and slow by two different mechanisms , 2016, Nature chemistry.