About: First total synthesis of ent-gelsedine via a novel iodide-promoted allene N-acyliminium ion cyclization

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About: First total synthesis of ent-gelsedine via a novel iodide-promoted allene N-acyliminium ion cyclization Goto Sponge NotDistinct Permalink

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scientific article published on 01 December 2000

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 2000 (uk) مقالة علمية تنشرت ف 1 دجنبر 2000 (ary) article scientifique publié en 2000 (fr) im Dezember 2000 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'avientu de 2000 (ast) scientific article published on 01 December 2000 (en) գիտական հոդված հրատարակված 2000 թվականի դեկտեմբերի 1-ին (hy)
publication date	wds:Q73255787-7A3B0C46-457E-4900-98B2-3C92877E883D
publication date	2000-12-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q73255787-A971B19D-FE4D-4DE5-984D-89A45AFB6B9C
language of work or name	English
cites work	wds:Q73255787-4512EC85-C961-4BEC-A38E-2087A647A387
cites work	THREE MINOR ALKALOIDS OF GELSEMIUMSEMPERVIRENS AIT.
author name string	wds:Q73255787-1DB6D523-2467-49D3-BB4B-9BBC50DEB6FD wds:Q73255787-25A58D51-4613-43F8-B230-BDE446B24BA1 wds:Q73255787-61E8A589-8127-4B1B-928F-41E313C33ED0 wds:Q73255787-BE12B614-C4E5-484C-80CD-694C932CFFE2
author name string	F P Rutjes H Hiemstra R M Fieseler W G Beyersbergen van Henegouwen
rdfs:label	First total synthesis of ent-gelsedine via a novel iodide-promoted allene N-acyliminium ion cyclization (en) First total synthesis of ent-gelsedine via a novel iodide-promoted allene N-acyliminium ion cyclization (nl)
skos:prefLabel	First total synthesis of ent-gelsedine via a novel iodide-promoted allene N-acyliminium ion cyclization (en) First total synthesis of ent-gelsedine via a novel iodide-promoted allene N-acyliminium ion cyclization (nl)
name	First total synthesis of ent-gelsedine via a novel iodide-promoted allene N-acyliminium ion cyclization (en) First total synthesis of ent-gelsedine via a novel iodide-promoted allene N-acyliminium ion cyclization (nl)
title	wds:Q73255787-0A083BFA-8F3B-4248-B3A1-45EE54AD2B33
title	First total synthesis of ent-gelsedine via a novel iodide-promoted allene N-acyliminium ion cyclization (en)
page(s)	wds:Q73255787-ACB33FAA-A4D9-43C3-8992-57D147C2BB21
page(s)	8317-8325
instance of	wds:Q73255787-4D5C2D10-AB8F-4C64-BD51-A6C4C9B7561F
instance of	scholarly article
PubMed ID	wds:Q73255787-9DEF91F2-17D1-40C9-BA7D-E67BB9DC05D8
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11101391
PubMed ID	11101391
published in	wds:Q73255787-74E654F0-5A9E-4A37-9218-EBC273D659DE
published in	Journal of Organic Chemistry
issue	wds:Q73255787-05937A53-46A3-40A3-B3D0-CD33DC1B5CD0
volume	wds:Q73255787-DF2A33E7-1387-4BF0-A2DD-7E2DD4D73308
issue	24
volume	65
DOI	wds:Q73255787-BFA4C8C8-5F2C-450F-989F-EBE30BBDAE00
DOI	http://dx.doi.org/10.1021/JO001119T
DOI	10.1021/JO001119T
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q73255787
is cites work of	Carbamoyl radical-mediated synthesis and semipinacol rearrangement of β-lactam diols. Aza-cope rearrangement-mannich cyclizations for the formation of complex tricyclic amines: stereocontrolled total synthesis of (+/-)-gelsemine. Synthesis, Biological and In Silico Evaluation of Pure Nucleobase-Containing Spiro (Indane-Isoxazolidine) Derivatives as Potential Inhibitors of MDM2-p53 Interaction Total Synthesis of Gelsenicine via a Catalyzed Cycloisomerization Strategy Highly Efficient and Stereoselective Construction of Bispirooxindole Derivatives via a Three-Component 1,3-Dipolar Cycloaddition Reaction Concise Total Synthesis of (-)-Affinisine Oxindole, (+)-Isoalstonisine, (+)-Alstofoline, (-)-Macrogentine, (+)-Na -Demethylalstonisine, (-)-Alstonoxine A, and (+)-Alstonisine.
is cites work of	wds:Q92571178-746FA97C-7BD0-4A3F-A129-5C30FDA196A3 wds:Q47712136-76564FF2-A9C7-49B8-A266-CB91E0AFAB95 wds:Q33913468-857D4A81-B7D9-41CF-963E-09AE71F964F6 wds:Q35061109-04308360-34C3-40E2-81B0-869B9C23C360 wds:Q36943652-8A0FA3B1-3F3A-4C69-8244-540A80A19A9A wds:Q36518529-E7A6554B-65F6-4198-AE09-734FE8F280A5

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