Simple indole alkaloids and those with a non-rearranged monoterpenoid unit
about
Selective syntheses of leuconolam, leuconoxine, and mersicarpine alkaloids from a common intermediate through regiocontrolled cyclizations by Staudinger reactions†Electronic supplementary information (ESI) available: Experimental details and proceduTotal Synthesis of Verruculogen and Fumitremorgin A Enabled by Ligand-Controlled C-H BorylationDirect C7 Functionalization of Tryptophan. Synthesis of Methyl (S)-2-((tert-Butoxycarbonyl)amino)-3-(7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indol-3-yl)propanoate.Total syntheses of the monoterpene indole alkaloids (±)-alstilobanine A and E and (±)-angustilodine.Sesquiterpenyl indoles.Applications of Bartoli indole synthesis.Strategies for the asymmetric functionalization of indoles: an update.The Diaza[5.5.6.6]fenestrane Skeleton-Synthesis of Leuconoxine Alkaloids.Microindolinone A, a Novel 4,5,6,7-Tetrahydroindole, from the Deep-Sea-Derived Actinomycete Microbacterium sp. MCCC 1A11207.Multicomponent syntheses of functional chromophores.Four-component strategy for selective synthesis of azepino[5,4,3-cd]indoles and pyrazolo[3,4-b]pyridinesBiomimetic Total Syntheses of (-)-Leucoridines A and C through the Dimerization of (-)-DihydrovalparicineC7-derivatization of C3-alkylindoles including tryptophans and tryptamines.Biosynthetically inspired divergent approach to monoterpene indole alkaloids: total synthesis of mersicarpine, leuconodines B and D, leuconoxine, melodinine E, leuconolam, and rhazinilam.Indole diterpenoid natural products as the inspiration for new synthetic methods and strategiesSynthesis of functionalised azepanes and piperidines from bicyclic halogenated aminocyclopropane derivatives.Predictive Model for Site-Selective Aryl and Heteroaryl C-H Functionalization via Organic Photoredox Catalysis.The synthesis of polysubstituted indoles from 3-bromo-2-indolyl phosphates.Gold-Catalyzed Divergent Ring-Closing Modes of Indole-Tethered Amino Allenynes.Synthesis of 1,1'- and 2,2'-Bicarbazole Alkaloids by Iron(III)-Catalyzed Oxidative Coupling of 2- and 1-Hydroxycarbazoles.Natural product inspired design and synthesis of β-carboline and γ-lactone based molecular hybrids.Palladium-catalyzed oxidative arylacetoxylation of alkenes: synthesis of indole and indoline derivatives.Total synthesis of architecturally complex indole terpenoids: strategic and tactical evolution.Amine-Catalyzed Highly Regioselective and Stereoselective C(sp(2) )-C(sp(2) ) Cross-Coupling of Naphthols with trans-α,β-Unsaturated Aldehydes.Divergent synthesis of indoles, oxindoles, isocoumarins and isoquinolinones by general Pd-catalyzed retro-aldol/α-arylation.Rhodium(III)-catalyzed C-H activation and indole synthesis with hydrazone as an auto-formed and auto-cleavable directing group.Palladium-catalyzed one-pot three- or four-component coupling of aryl iodides, alkynes, and amines through C-N bond cleavage: efficient synthesis of indole derivatives.Synthesis of N-alkyl-3-sulfonylindoles and N-alkyl-3-sulfanylindoles by cascade annulation of 2-alkynyl-N,N-dialkylanilines.Copper-catalyzed annulation of α-substituted diazoacetates with 2-ethynylanilines: the direct synthesis of C2-functionalized indoles.Copper-mediated C3-cyanation of indoles by the combination of amine and ammonium.Reactivity of alkynylindole-2-carboxamides in [Pd]-catalysed C-H activation and phase transfer catalysis: formation of pyrrolo-diindolones vs. β-carbolinones.Formal [4+2] Reaction between 1,3-Diynes and Pyrroles: Gold(I)-Catalyzed Indole Synthesis by Double HydroarylationEfficient Synthesis of Indole Derivatives via Tandem Cyclization Catalyzed by Magnetically Recoverable Palladium/Magnetite (Pd-Fe3 O4 ) NanocrystalsTandem cyclisation of vinyl radicals: a sustainable approach to indolines utilizing visible-light photoredox catalysis
P2860
Q30900334-B6FEFE54-E226-4E78-BBB6-727831015A2AQ34488881-632CAB0B-A510-4BDC-BE32-52B6990505CFQ36523616-9D5D7AE3-2DA7-4978-B9E3-6951F3F7B76DQ37552552-1E8568BB-CA0F-4D32-B5C0-0F325929F3E4Q38156579-7218A8BF-B8C6-4207-B358-177CEF5A0616Q38203462-A333FA7C-4A3F-4828-826A-8E69E9298EB4Q38260296-56A30856-4806-4115-98A6-E893D9AE0EE7Q38601285-550B6E64-2FFB-4DF4-944E-11EE539A659BQ38654921-A8BB96EB-8513-4AD0-A5CA-8703FF6B11F4Q38742514-F303B19A-6FDB-4AE4-90B4-F5949CE4B70CQ40787385-71841FF2-B232-4480-A91D-A7E5EF3C0B6FQ41020714-09256AF2-FCBF-4E56-91C7-5EF1B324B93EQ41886377-CFC3BAB2-997C-41BC-A7AD-8A80DA6963C6Q42114260-BDC6FE5D-1BAF-4B3F-876C-18C1E1DA7BCDQ42124587-FE84AAAD-538B-487B-ACB2-DB041DB19E79Q46349707-EB1CE4C0-F8EB-4B22-94B0-66BEC11A5B6CQ48109840-8519FC85-CA60-4357-BB66-FF15C999FDC0Q48135073-68429E5E-0329-41FC-88DF-215BE17F4F0EQ48154537-75261E05-F053-4F67-B35E-91141810AAADQ48200273-73FA4CA2-EA71-4595-AAC8-00424D38D833Q49124404-EC8BE003-12AA-4906-AACB-47547AACDABEQ49686840-7B91960A-AA28-4B09-9990-73EB9340EF1BQ50277018-B6DDE1F7-8D66-4440-BB13-E4367C0EB765Q50961300-7C7F43E1-FAF6-491A-9D72-90401A6ACA88Q51130533-71F2FEAA-B36B-4C38-97F3-5839FF9D649DQ51756801-4CC6130A-0516-4676-87E9-5D43CBE2CE7AQ52765256-072289E8-5318-4CA2-82FB-5D0CA6DFDC50Q53364389-F1C17573-E6D7-492F-806D-AE71E945D365Q53633898-F3DA84F8-269C-4372-B6CB-6CE24B94C3C5Q53635928-1BF48237-B1C8-496D-9086-96855C6AEE00Q54029277-42D2C224-E599-44A7-AFA9-24F1359F816DQ57261440-C319E799-521E-49CC-A96E-FD53DE544C7BQ57557935-531E4634-3314-4495-BCFF-4877DF1C7BABQ58214000-6CCA61F1-A947-4477-B5C8-689404447234
P2860
Simple indole alkaloids and those with a non-rearranged monoterpenoid unit
description
im Januar 2013 veröffentlichter wissenschaftlicher Artikel
@de
scientific article published on 01 May 2013
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована у 2013
@uk
name
Simple indole alkaloids and those with a non-rearranged monoterpenoid unit
@en
Simple indole alkaloids and those with a non-rearranged monoterpenoid unit
@nl
type
label
Simple indole alkaloids and those with a non-rearranged monoterpenoid unit
@en
Simple indole alkaloids and those with a non-rearranged monoterpenoid unit
@nl
prefLabel
Simple indole alkaloids and those with a non-rearranged monoterpenoid unit
@en
Simple indole alkaloids and those with a non-rearranged monoterpenoid unit
@nl
P2093
P2860
P356
P1476
Simple indole alkaloids and those with a non-rearranged monoterpenoid unit
@en
P2093
Minoru Ishikura
Satoshi Hibino
Tominari Choshi
P2860
P304
P356
10.1039/C3NP20118J
P50
P577
2013-05-01T00:00:00Z