About: The first regiospecific, enantiospecific total synthesis of 6-oxoalstophylline and an improved total synthesis of alstonerine and alstophylline as well as the bisindole alkaloid macralstonine

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About: The first regiospecific, enantiospecific total synthesis of 6-oxoalstophylline and an improved total synthesis of alstonerine and alstophylline as well as the bisindole alkaloid macralstonine Goto Sponge NotDistinct Permalink

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scientific article published on 01 August 2005

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2005 (fr) наукова стаття, опублікована в серпні 2005 (uk) artículu científicu espublizáu n'agostu de 2005 (ast) scientific article published on 01 August 2005 (en)
publication date	wds:Q80945376-1E75DFAD-9EBB-4929-8C5A-1F6C708F7C25
publication date	2005-08-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q80945376-483EC320-DF6F-4BB9-98E3-AFA8AD685061
cites work	In vitro antiamoebic and antiplasmodial activities of alkaloids isolated fromAlstonia angustifolia roots
author name string	wds:Q80945376-0421D7F7-5656-4D9B-AA49-0AD89ADC5DFE wds:Q80945376-552D7AA4-B514-4335-8624-4444280D3C0B wds:Q80945376-8DB2402F-822B-4BF7-BCE2-EB5701FA643F wds:Q80945376-ACC02018-651B-4C26-8635-6D0ABFDF93D7 wds:Q80945376-CB29B66D-CA94-4A27-B397-9ACA2C956724
author name string	Hao Zhou Jun Ma James M Cook Xuebin Liao Xiangyu Z Wearing
rdfs:label	The first regiospecific, enantiospecific total synthesis of 6-oxoalstophylline and an improved total synthesis of alstonerine and alstophylline as well as the bisindole alkaloid macralstonine (en) The first regiospecific, enantiospecific total synthesis of 6-oxoalstophylline and an improved total synthesis of alstonerine and alstophylline as well as the bisindole alkaloid macralstonine (nl)
skos:prefLabel	The first regiospecific, enantiospecific total synthesis of 6-oxoalstophylline and an improved total synthesis of alstonerine and alstophylline as well as the bisindole alkaloid macralstonine (en) The first regiospecific, enantiospecific total synthesis of 6-oxoalstophylline and an improved total synthesis of alstonerine and alstophylline as well as the bisindole alkaloid macralstonine (nl)
name	The first regiospecific, enantiospecific total synthesis of 6-oxoalstophylline and an improved total synthesis of alstonerine and alstophylline as well as the bisindole alkaloid macralstonine (en) The first regiospecific, enantiospecific total synthesis of 6-oxoalstophylline and an improved total synthesis of alstonerine and alstophylline as well as the bisindole alkaloid macralstonine (nl)
title	wds:Q80945376-06091C56-F95E-479A-AF6D-FFC6176F09E3
title	The first regiospecific, enantiospecific total synthesis of 6-oxoalstophylline and an improved total synthesis of alstonerine and alstophylline as well as the bisindole alkaloid macralstonine (en)
page(s)	wds:Q80945376-6A0A0505-B17C-4F73-88A8-67CDD40512D4
page(s)	3501-3504
instance of	wds:Q80945376-D944E0C8-BEBF-4ED3-BCEA-FC2BFB983524
instance of	scholarly article
PubMed ID	wds:Q80945376-316A8141-2AF0-4557-9CBB-B5A681691360
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16048327
PubMed ID	16048327
published in	wds:Q80945376-BEB9D54C-0998-49A9-B1B7-14D1C28599A1
published in	Organic Letters
issue	wds:Q80945376-F1CB6887-9F7E-4BF5-B644-2AB06FAA646F
volume	wds:Q80945376-BA67DC1C-4A22-4F00-A56E-70A92C1E9379
issue	16
volume	7
DOI	wds:Q80945376-9600DAD8-316C-4B45-BD8F-35966B013E69
DOI	http://dx.doi.org/10.1021/OL051208Y
DOI	10.1021/OL051208Y
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q80945376
is cites work of	Concise, enantioselective total synthesis of (-)-alstonerine Sarpagine and Related Alkaloids A divergent strategy for the synthesis of secologanin derived natural products Stereospecific total synthesis of the indole alkaloid ervincidine. Establishment of the C-6 hydroxyl stereochemistry A two step synthesis of BzR/GABAergic active flavones via a Wacker-related oxidation Study of the cis to trans isomerization of 1-phenyl-2,3-disubstituted tetrahydro-beta-carbolines at C(1). Evidence for the carbocation-mediated mechanism Concise Total Synthesis of (-)-Affinisine Oxindole, (+)-Isoalstonisine, (+)-Alstofoline, (-)-Macrogentine, (+)-Na -Demethylalstonisine, (-)-Alstonoxine A, and (+)-Alstonisine. The Pauson-Khand Reaction as a New Entry to the Synthesis of Bridged Bicyclic Heterocycles: Application to the Enantioselective Total Synthesis of (-)-Alstonerine Synthesis of Bisindole Alkaloids from the Apocynaceae Which Contain a Macroline or Sarpagine Unit: A Review Enantioselective Total Syntheses of Methanoquinolizidine-Containing Akuammiline Alkaloids and Related Studies. Enantioselective total syntheses of (+)-stemofoline and three congeners based on a biogenetic hypothesis
is cites work of	wds:Q38201747-35FA00BA-90CA-45AF-9C4F-180EB58AAC28 wds:Q41845290-C58AB922-E3E4-4FC1-BA34-D9997A2EE003 wds:Q47712136-BD976216-2BFB-4596-BEBD-B7FFF125BDFC wds:Q28073089-A664D433-AD4D-4474-B89B-075AB3C1CB8F wds:Q100750132-079901BE-0B02-4C76-9FDE-FE336C740270 wds:Q36838696-64A4652C-6235-4A1C-A1D5-259D3759BFB4 wds:Q26772946-9E207A1A-1E34-4A23-B44F-695ADF82A2A0 wds:Q52563997-E2C3E405-91D5-414E-8EDD-849A3DA16280 wds:Q34569927-021D1A5D-2CC8-4A9A-8B5C-88AF7B286230 wds:Q42578611-18F7A7CD-5BD8-45D0-BBC1-10916E434B35 wds:Q36837747-83FEB518-BA50-4DCD-8082-E04AB9D6B088

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