Enantioselective total synthesis of avrainvillamide and the stephacidins.
about
Molecular rearrangements in the construction of complex moleculesTotal synthesis of (+/-)-actinophyllic acidRadicals: Reactive Intermediates with Translational PotentialInnate and Guided C–H Functionalization LogicStudies on the Biosynthesis of the Stephacidin and Notoamide Natural Products: A Stereochemical and Genetic ConundrumIsolation, structure elucidation, and biomimetic total synthesis of versicolamide B, and the isolation of antipodal (-)-stephacidin A and (+)-notoamide B from Aspergillus versicolor NRRL 35600.Synthetic approaches to the bicyclo[2.2.2]diazaoctane ring system common to the paraherquamides, stephacidins and related prenylated indole alkaloids.Total Synthesis of Verruculogen and Fumitremorgin A Enabled by Ligand-Controlled C-H BorylationEvidence for the rapid conversion of stephacidin B into the electrophilic monomer avrainvillamide in cell culture.Enantioselective route to platensimycin: an intramolecular Robinson annulation approachOn the nature of the oxidative heterocoupling of lithium enolates.Natural products synthesis: enabling tools to penetrate Nature's secrets of biogenesis and biomechanism.Total synthesis of the Galbulimima alkaloid (-)-GB17Concise, Biomimetic Total Synthesis of d,l-Marcfortine C.Oxidative Coupling of Enolates, Enol Silanes and Enamines: Methods and Natural Product Synthesis.Concise, asymmetric, stereocontrolled total synthesis of stephacidins A, B and notoamide BScope and mechanism of direct indole and pyrrole couplings adjacent to carbonyl compounds: total synthesis of acremoauxin A and oxazinin 3.Premalbrancheamide: synthesis, isotopic labeling, biosynthetic incorporation, and detection in cultures of Malbranchea aurantiaca.Intermolecular Diels-Alder Cycloaddition for the Construction of Bicyclo[2.2.2]diazaoctane Structures: Formal Synthesis of Brevianamide B and PremalbrancheamideStereoselective Synthesis of Quaternary Proline Analogues.Chemoselectivity: the mother of invention in total synthesis.Recent synthetic approaches towards the antiproliferative natural products avrainvillamide and stephacidin B.2-Iodoxybenzoic acid--a simple oxidant with a dazzling array of potential applications.Recent advances in target characterization and identification by photoaffinity probes.Natural product synthesis in the age of scalability.Iron-promoted C-C bond formation in the total synthesis of natural products and drugs.Natural product analogues: towards a blueprint for analogue-focused synthesis.Total synthesis of (+/-)- and (-)-actinophyllic acid.Direct, chemoselective N-tert-prenylation of indoles by C-H functionalization.Intramolecular C(sp3)-N coupling by oxidation of benzylic C,N-dianionsAn improved synthesis of alpha,beta-unsaturated nitrones relevant to the stephacidins and analogs thereof.Unified Approach to Prenylated Indole Alkaloids: Total Syntheses of (-)-17-Hydroxy-Citrinalin B, (+)-Stephacidin A, and (+)-Notoamide I.Mechanistic study on the palladium(II)-catalyzed synthesis of 2,3-disubstituted indoles under aerobic conditions: anion effects and the development of a low-catalyst-loading process.Bioinspired chemical synthesis of monomeric and dimeric stephacidin A congeners.Total Synthesis of Notoamides F, I, and R and Sclerotiamide.Total synthesis of (-)-depyranoversicolamide B.The cascade radical cyclisation approach to prenylated alkaloids: synthesis of stephacidin A and notoamide B.Biogenetic hypothesis and first steps towards a biomimetic synthesis of haouaminesStructural and stereochemical diversity in prenylated indole alkaloids containing the bicyclo[2.2.2]diazaoctane ring system from marine and terrestrial fungi
P2860
Q24610464-CA232BF9-8C60-46C5-BA04-C750BECF6CFBQ24642045-9C5398A3-BB04-4473-B39C-B299E38C1F5DQ28468198-3F47D70F-B9D5-4DD5-9622-68550CF5FCFCQ30054500-1887F277-4B1B-4375-BDB2-20C82644AFECQ33351935-A8B66AEB-6D38-4C7D-B094-986BBC2C3273Q33692567-0C355CFC-9732-4B17-8414-B9FC09D2911FQ33731803-30E64AFF-86D1-4FB1-962A-088AB84B8CDCQ34488881-7DDF023B-B685-4DFC-A68A-BC1D7B133708Q34614087-356D925A-C91F-43C6-ABEF-D8FA80861718Q34650738-D5EA78CC-818F-407E-9755-12CC18ADF18FQ35132089-8A00B704-0731-4253-B92E-309D0AB20C7AQ35215703-63A86C45-A871-4051-99DB-AC58E8418C11Q36401433-783FC043-5C77-4D96-9C87-F0B40820D0E7Q36593361-F936221F-ECCF-4337-BC1A-FA11F5529185Q36652114-7A89926B-C6EF-4634-9E02-37379A0CD10CQ36854667-10DB812A-0EF2-40F4-A9EE-E8E6CEA90B93Q37074026-1B16F06F-5807-468B-B5AD-F971411E2116Q37117923-5282D6CC-B20B-4C2E-8A08-3B8164BD52E5Q37193962-F75FE948-683F-4F39-AB7C-7036ADAA002DQ37286829-CBDD522F-35A2-4B41-9BC7-8B5B3ED43661Q37395761-0DF186C3-BEA6-4C02-AFE1-67C0AF89C603Q37683487-3DD2B4A1-E409-40D6-96BA-93867F40CD23Q37832721-EEA70FF2-FA68-4480-8AAF-D28FBC87BA30Q38133223-3607DA0E-F38F-46DB-A4DF-FFBFA9700543Q38171270-B372E2BB-60E2-4D69-AE95-798E9B217E9EQ38591197-65589386-09C6-423F-A1C9-8997C966418BQ39413228-D62430A5-D26B-4412-8CDE-16CA74C1DD97Q39957823-945F27E4-369F-4C91-8BF6-18C7F12B6FB5Q41104824-AAED8D5D-5971-4B04-AECC-042B437129FBQ41865996-8B28E4E0-B691-45E4-ADB2-7A7896266AA9Q42137595-3C583C93-151B-4320-BE97-44803A3BBD9AQ42244479-01AAA6B8-F646-4106-896E-7DDEE4358067Q46853925-AC8702A5-8CA1-4525-ACF6-CD338C3630CEQ48095543-24919215-44C0-4579-AE15-DCA9418ADF25Q48148786-F2C0C782-B292-454E-9804-47C19CD9576CQ51711930-ADFE46C0-78D6-4509-891D-4A53E38F675BQ51802203-B38B551F-ED95-4C60-AC80-8161077B3B2CQ56745087-A6A5180E-36FC-4028-BFAF-B0A3E8BA83FDQ59140396-F53733D2-15F3-4779-9B19-861AB1AB01FD
P2860
Enantioselective total synthesis of avrainvillamide and the stephacidins.
description
2006 nî lūn-bûn
@nan
2006 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Enantioselective total synthesis of avrainvillamide and the stephacidins.
@ast
Enantioselective total synthesis of avrainvillamide and the stephacidins.
@en
Enantioselective total synthesis of avrainvillamide and the stephacidins.
@nl
type
label
Enantioselective total synthesis of avrainvillamide and the stephacidins.
@ast
Enantioselective total synthesis of avrainvillamide and the stephacidins.
@en
Enantioselective total synthesis of avrainvillamide and the stephacidins.
@nl
prefLabel
Enantioselective total synthesis of avrainvillamide and the stephacidins.
@ast
Enantioselective total synthesis of avrainvillamide and the stephacidins.
@en
Enantioselective total synthesis of avrainvillamide and the stephacidins.
@nl
P2093
P356
P1476
Enantioselective total synthesis of avrainvillamide and the stephacidins.
@en
P2093
Benjamin D Hafensteiner
Carlos A Guerrero
John D Gallagher
Narendra B Ambhaikar
Phil S Baran
P304
P356
10.1021/JA061660S
P407
P577
2006-07-01T00:00:00Z