Total Synthesis of Nominal Diazonamides-Part 1: Convergent Preparation of the Structure Proposed for (-)-Diazonamide A Funding provided by the NIH (RO1-GM60591), the NSF (CAREER 9984282), the Howard Hughes Medical Institute (junior faculty support),

Total Synthesis of Nominal Diazonamides-Part 1: Convergent Preparation of the Structure Proposed for (-)-Diazonamide A Funding provided by the NIH (RO1-GM60591), the NSF (CAREER 9984282), the Howard Hughes Medical Institute (junior faculty support),

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http://www.wikidata.org/entity/Q34156614

Q34156614

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Therapeutic anticancer efficacy of a synthetic diazonamide analog in the absence of overt toxicity.Total Synthesis of Nominal Diazonamides-Part 2: On the True Structure and Origin of Natural Isolates Funding provided by the NIH (RO1-GM60591), the NSF (CAREER 9984282), the Howard Hughes Medical Institute (junior faculty support), the Robert A. Wel Interactions of antimitotic peptides and depsipeptides with tubulin.Diazonamide toxins reveal an unexpected function for ornithine delta-amino transferase in mitotic cell division.Constructing molecular complexity and diversity: total synthesis of natural products of biological and medicinal importance.A concise formal synthesis of diazonamide A by the stereoselective construction of the C10 quaternary center Structural characterization of an enantiomerically pure amino acid imidazolide and direct formation of the beta-lactam nucleus from an alpha-amino acid.Total synthesis of atrochamins F, H, I, and J through cascade reactions.Diazonamide support studies: stereoselective formation of the C10 chiral center in both the CDEFG and AEFG fragments Total syntheses of hopeanol and hopeahainol A empowered by a chiral Brønsted acid induced pinacol rearrangement.Enantioselective organocatalytic construction of pyrroloindolines by a cascade addition-cyclization strategy: synthesis of (-)-flustramine B.The Witkop cyclization: a photoinduced C-H activation of the indole system.An expedient formal total synthesis of (-)-diazonamide A via a powerful, stereoselective O-aryl to C-aryl migration to form the C10 quaternary center.Electrolytic macrocyclizations: scalable synthesis of a diazonamide-based drug development candidate.Efficient approach to 2-hydroxy-2,3-dihydrofuran derivatives and its application for the synthesis of novel 4-(1H-pyrazol-4-yl)pyridazines.One-step formation of dihydrofuranoindoline cores promoted by a hypervalent iodine reagent.Pardon the Interruption: A Modification of Fischer's Venerable Reaction for the Synthesis of Heterocycles and Natural Products.C4-H indole functionalisation: precedent and prospects.Gold-catalysed synthesis of amino acid-derived 2,5-disubstituted oxazoles

P2860

Q30478959-21DEEDD7-F8BB-4EB0-827A-D0E84C69A6B5 Q34156618-E828F062-B816-4A50-BF82-5F182BFBD247 Q34972878-3A9E1CF4-F2F1-49F8-ABB8-1FF6BFEDBD0A Q35846534-0D55AD8C-E5EE-4CD5-9B48-4FFB8AF47AA8 Q36186718-C237EDD8-603E-4271-9F5D-8E8795DBE264 Q36519963-4FC137AE-1D05-410F-9A48-7031C939EABB Q37003105-2403F77C-DC0D-40E2-9F33-195C243B7DFA Q37004298-49C8C760-FF13-4921-8FCA-364AA95EC1C6 Q37089141-9474DA85-B5D4-44D5-8A6A-D3E49B57B691 Q37098622-25B41B3F-8E7D-4B35-9F74-D2F37265A977 Q37681767-19818EC8-34FD-4027-9EDC-537555602899 Q38170051-D0282FCA-EBBF-46B1-9F25-D55ED37FD7BD Q41899975-8963EFE7-5350-42ED-B2E9-E212EE60F939 Q46293337-A212912D-29A2-4CD1-A886-8C4E31F70966 Q50994772-2258E054-747B-4C53-BF32-E08385F5F9A6 Q52682187-BEE1F429-568E-40DB-ACCD-2B8A1020A303 Q55312180-1C79CADC-2D26-4951-AC03-F9AC48B0DA28 Q55447796-34E4F7B3-4290-4247-8C6C-AD3F4C0FB2AB Q58195187-C1D02C31-CFFF-45C3-BB58-AF07A0DE1DE4

P2860

Total Synthesis of Nominal Diazonamides-Part 1: Convergent Preparation of the Structure Proposed for (-)-Diazonamide A Funding provided by the NIH (RO1-GM60591), the NSF (CAREER 9984282), the Howard Hughes Medical Institute (junior faculty support),

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http://www.wikidata.org/entity/Q34156614

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2001 nî lūn-bûn

@nan

2001 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2001 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2001年の論文

@ja

2001年論文

@yue

2001年論文

@zh-hant

2001年論文

@zh-hk

2001年論文

@zh-mo

2001年論文

@zh-tw

2001年论文

@wuu