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Biologically active vallesamine, strychnan, and rhazinilam alkaloids from Alstonia: Pneumatophorine, a nor-secovallesamine with unusual incorporation of a 3-ethylpyridine moiety.Hispidacine, an unusual 8,4'-oxyneolignan-alkaloid with vasorelaxant activity, and hispiloscine, an antiproliferative phenanthroindolizidine alkaloid, from Ficus hispida Linn.Angustilobine and andranginine type indole alkaloids and an uleine-secovallesamine bisindole alkaloid from Alstonia angustiloba.Ibogan, Aspidosperman, Vincamine, and Bisindole Alkaloids from a Malayan Tabernaemontana corymbosa: Iboga Alkaloids with C-20α Substitution.Arborisidine and Arbornamine, Two Monoterpenoid Indole Alkaloids with New Polycyclic Carbon-Nitrogen Skeletons Derived from a Common Pericine Precursor.Vobatensines A-F, Cytotoxic Iboga-Vobasine Bisindoles from Tabernaemontana corymbosa.Aspidospermatan-aspidospermatan and eburnane-sarpagine bisindole alkaloids from Leuconotis.Leuconicines A-G and (-)-eburnamaline, biologically active strychnan and eburnan alkaloids from Leuconotis.Cytotoxic vobasine, tacaman, and corynanthe-tryptamine bisindole alkaloids from Tabernaemontana and structure revision of tronoharine.Macroline, akuammiline, sarpagine, and ajmaline alkaloids from Alstonia macrophylla.Aspidofractinine and Eburnane Alkaloids from a North Borneo Kopsia. Ring-Contracted, Additional Ring-Fused, and Paucidactine-Type Aspidofractinine Alkaloids from K. pauciflora.Ibogan, tacaman, and cytotoxic bisindole alkaloids from tabernaemontana. Cononusine, an iboga alkaloid with unusual incorporation of a pyrrolidone moiety.Arboridinine, a Pentacyclic Indole Alkaloid with a New Cage Carbon-Nitrogen Skeleton Derived from a Pericine Precursor.Corynanthean, eburnan, secoleuconoxine, and pauciflorine alkaloids from Kopsia pauciflora.Lumutinines A-D, linearly fused macroline-macroline and macroline-sarpagine bisindoles from Alstonia macrophyllaGrandilodines A-C, biologically active indole alkaloids from Kopsia grandifoliaPerhentidines A-C: macroline-macroline bisindoles from Alstonia and the absolute configuration of perhentinine and macralstonineOxidized derivatives of macroline, sarpagine, and pleiocarpamine alkaloids from Alstonia angustifoliaTransformations of Ferric Chloride-Generated Stilbene Cation Radicals. The Effect of Aromatic Substitution and a Comparison with Anodic OxidationLumusidines A-D and villalstonidine F, macroline-macroline and macroline-pleiocarpamine bisindole alkaloids from Alstonia macrophyllaCriofolinine and vernavosine, new pentacyclic indole alkaloids incorporating pyrroloazepine and pyridopyrimidine moieties derived from a common yohimbine precursorRhazinilam-Leuconolam-Leuconoxine Alkaloids from Leuconotis griffithiiTransformations of the 2,7-Seco Aspidosperma alkaloid leuconolam, structure revision of epi-leuconolam, and partial syntheses of leuconoxine and leuconodines A and FVoatinggine and tabertinggine, pentacyclic indole alkaloids derived from an iboga precursor via a common cleavamine-type intermediateBiomimetic oxidative dimerization of anodically generated stilbene radical cations: effect of aromatic substitution on product distribution and reaction pathwaysAndransinine: an unusual case of spontaneous resolution in an indole alkaloid derivativeAlstoscholactine and Alstolaxepine, Monoterpenoid Indole Alkaloids with γ-Lactone-Bridged Cycloheptane and Oxepane Moieties from Alstonia scholarisMacroline-Sarpagine Bisindole Alkaloids with Antiproliferative Activity from Alstonia penangianaLycopodium Alkaloids: Lycoplatyrine A, an Unusual Lycodine-Piperidine Adduct from Lycopodium platyrhizoma and the Absolute Configurations of Lycoplanine D and Lycogladine HReactions of Anodically Generated Methoxystilbene Cation Radicals: The Influence of Ortho-Substituted Vinyl and Formyl GroupsConolodinines A-D, Aspidosperma- Aspidosperma Bisindole Alkaloids with Antiproliferative Activity from Tabernaemontana corymbosaSchwarzinicines A-G, 1,4-Diarylbutanoid-Phenethylamine Conjugates from the Leaves of Ficus schwarziiA Cytotoxic Indole Characterized by Incorporation of a Unique Carbon-Nitrogen Skeleton and Two Pentacyclic Corynanthean Alkaloids Incorporating a Substituted Tetrahydrofuranone Ring from Kopsia arboreaReactivity of Anodically Generated 4-Methoxystilbene Cation Radicals: The Influence of Ortho-Substituted Hydroxymethyl, Aminomethyl, and Carboxylic Acid Groups
P50
Q38858460-13155890-A7B2-49ED-8720-C31AC764C380Q38932751-B3B7C2E4-664E-4C50-91C3-2D04D5D7C2B0Q39480136-8BA5F911-24BF-4E0A-8FD3-EF051D9BC704Q39851492-BDA5A7AE-32E8-420B-A7F7-13FCBDA2D27FQ39873482-6A9CC919-55A2-4C31-BEE3-90FEAF291AE9Q39966182-635161F7-9625-4C67-B0D9-59D3D6EADFACQ43028026-4A1B3B38-0B2B-4A23-A96F-E03DAA93DF21Q43207491-399D62BA-3EA2-4150-854D-A7492485A34DQ46019352-1684F474-9A5B-4519-B96E-89C673FB8564Q46550596-29961886-3940-4994-8F23-5EC9C7850075Q51584684-17FF031E-9501-4EAB-8B74-21CC5BE41B96Q52947781-600D00B4-50AD-49E6-8C9B-184C535B02CAQ53181074-118C1F0D-8119-48F4-A424-7652117BD999Q53379942-9AC3B451-504C-4967-A527-A885C4ACDA23Q82841097-7F002187-9FB1-4462-B0AE-EB68D139EE0CQ83685685-DBE455FC-9952-4508-8A04-AB03AD806ED2Q84072102-4B57D21C-2F25-4635-955F-C5CC96F267DBQ85292577-CA4B341D-4392-4FF1-96B3-209EF7F0A1F7Q85419653-BA82C17F-3C78-4223-85AD-6FA536CF437AQ85582489-51FF62DC-E3B2-4C44-8E86-82CF9FCAC1DFQ86122658-403D6BBF-B070-4D35-AD70-D57104FF9849Q86720383-F10D6A9B-6515-43E7-AD1A-50E9C095A44FQ87103813-BD5DED8D-B556-44A5-BDEC-034D8186A4B8Q87335040-AF9566E6-88A4-4C2B-81CF-23A8D799E224Q87728999-3BAB5302-E7D4-41AF-ACEF-9E3FEC0C0F77Q87885827-2661162B-0F45-4EB8-8152-43A4F4BC0AF8Q90447006-083B1087-FA41-4391-824A-20C7828B152EQ90898097-B0520B70-D33E-4650-BDDE-BD4EF8528E9EQ91276568-415E4797-14AE-47FC-A3EF-D385F89481F0Q91773752-B3A8AC1F-3F6B-441E-B9C5-4C98000C3057Q92354756-7BD03594-919A-4976-BE89-F43694F9AEEBQ92625556-7F5CDB7B-9466-4DB0-9351-4B628868C8E1Q93044071-B16AF1B1-B804-49F4-952A-88A123CAF0A2Q93387959-00799492-9DC4-44D1-919C-3070446428E1
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Yun-Yee Low
@ast
Yun-Yee Low
@en
Yun-Yee Low
@es
Yun-Yee Low
@nl
Yun-Yee Low
@sl
type
label
Yun-Yee Low
@ast
Yun-Yee Low
@en
Yun-Yee Low
@es
Yun-Yee Low
@nl
Yun-Yee Low
@sl
altLabel
Y.-Y. Low
@en
Yun Yee Low
@en
Yun-Yee Low
@en
prefLabel
Yun-Yee Low
@ast
Yun-Yee Low
@en
Yun-Yee Low
@es
Yun-Yee Low
@nl
Yun-Yee Low
@sl
P1053
J-9784-2016
P106
P31
P3829
P496
0000-0002-7429-4238