About: TiCl4 Promoted Three Component Coupling Reaction : A New Method for the Synthesis of Functionalized Tetrahydrofurans and Tetrahydropyrans

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About: TiCl4 Promoted Three Component Coupling Reaction : A New Method for the Synthesis of Functionalized Tetrahydrofurans and Tetrahydropyrans Goto Sponge NotDistinct Permalink

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scientific article published on 01 February 1999

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в лютому 1999 (uk) artículu científicu espublizáu en febreru de 1999 (ast) artikull shkencor i botuar më 01 shkurt 1999 (sq) scientific article published on 01 February 1999 (en)
publication date	wds:Q93029335-A5E21141-485C-48B4-82EA-3163377EE163
publication date	1999-02-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q93029335-096D0CCA-9B9B-4643-8046-45DEA246348C wds:Q93029335-AAABF66A-D33E-4BEF-9B00-C8C5C0C271E0
cites work	Potent HIV protease inhibitors: the development of tetrahydrofuranylglycines as novel P2-ligands and pyrazine amides as P3-ligands Tetrapropylammonium Perruthenate, Pr4N+RuO4 -, TPAP: A Catalytic Oxidant for Organic Synthesis
author name string	wds:Q93029335-1F2713F9-F2F0-4DBF-BD44-CF07A0B1DFA6 wds:Q93029335-D338314D-C648-43BA-9497-4C700570461B
author name string	Arun K Ghosh Reiko Kawahama
rdfs:label	TiCl4 Promoted Three Component Coupling Reaction : A New Method for the Synthesis of Functionalized Tetrahydrofurans and Tetrahydropyrans (en) TiCl4 Promoted Three Component Coupling Reaction : A New Method for the Synthesis of Functionalized Tetrahydrofurans and Tetrahydropyrans (nl) TiCl4 Promoted Three Component Coupling Reaction : A New Method for the Synthesis of Functionalized Tetrahydrofurans and Tetrahydropyrans (sq)
skos:prefLabel	TiCl4 Promoted Three Component Coupling Reaction : A New Method for the Synthesis of Functionalized Tetrahydrofurans and Tetrahydropyrans (en) TiCl4 Promoted Three Component Coupling Reaction : A New Method for the Synthesis of Functionalized Tetrahydrofurans and Tetrahydropyrans (nl) TiCl4 Promoted Three Component Coupling Reaction : A New Method for the Synthesis of Functionalized Tetrahydrofurans and Tetrahydropyrans (sq)
name	TiCl4 Promoted Three Component Coupling Reaction : A New Method for the Synthesis of Functionalized Tetrahydrofurans and Tetrahydropyrans (en) TiCl4 Promoted Three Component Coupling Reaction : A New Method for the Synthesis of Functionalized Tetrahydrofurans and Tetrahydropyrans (nl) TiCl4 Promoted Three Component Coupling Reaction : A New Method for the Synthesis of Functionalized Tetrahydrofurans and Tetrahydropyrans (sq)
title	wds:Q93029335-C0EC3067-2AB5-4FF7-9B02-51924818358A
title	TiCl4 Promoted Three Component Coupling Reaction : A New Method for the Synthesis of Functionalized Tetrahydrofurans and Tetrahydropyrans (en)
page(s)	wds:Q93029335-65D9CBB7-0DEE-4FF8-8867-602B78AAD4F4
page(s)	1083-1086
instance of	wds:Q93029335-800D4AFD-26DB-4294-9E3E-ACC379401613
instance of	scholarly article
PubMed ID	wds:Q93029335-1B3C63F3-8BBD-4618-9B1A-BAE24837BBC4
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/30422132
PubMed ID	30422132
published in	wds:Q93029335-6DB93F1B-2813-40A0-91F8-670ED24746E5
published in	Tetrahedron Letters
issue	wds:Q93029335-4B01D7EC-F5D5-44E3-85A2-6E44F1018E0E
volume	wds:Q93029335-CD38F861-604B-48D0-BAC9-97EF9AD82E96
issue	6
volume	40
DOI	wds:Q93029335-84D7E25E-D30D-44D4-A8BD-03F29E42B132
DOI	http://dx.doi.org/10.1016/S0040-4039(98)02633-1
DOI	10.1016/S0040-4039(98)02633-1
PMCID	wds:Q93029335-897FDBDF-C2E7-4A21-9655-2B5BA5B50803
PMCID	6226096
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q93029335
is cites work of	New reactions of 2-methylenetetrahydropyrans. A three component coupling protocol for the synthesis of tetrahydropyranyl ketides Harnessing nature's insight: design of aspartyl protease inhibitors from treatment of drug-resistant HIV to Alzheimer's disease Capturing the essence of organic synthesis: from bioactive natural products to designed molecules in today's medicine TiCl4-promoted tandem carbonyl or imine addition and Friedel-Crafts cyclization: synthesis of benzo-fused oxabicyclooctanes and nonanes Stereoselective construction of quaternary carbon centers by three component coupling reactions Nature Inspired Molecular Design: Stereoselective Synthesis of Bicyclic and Polycyclic Ethers for Potent HIV-1 Protease Inhibitors TiC14 promoted three component coupling reaction: an efficient method for the substituted tetrahydropyrilidene acetates Asymmetric multicomponent reactions: diastereoselective synthesis of substituted pyrrolidines and prolines Asymmetric multi-component reactions: convenient access to acyclic stereocenters and functionalized cyclopentenoids A stereoselective synthesis of (-)-viridiofungin A utilizing a TiCl(4)-promoted asymmetric multicomponent reaction
is cites work of	wds:Q35105355-CA610BE4-0847-4E66-BEC0-3A102D5B1FCA wds:Q90599603-0C934656-F886-4C76-AF5F-0585FCB0FA88 wds:Q93367088-BF54CF92-028C-4DE0-A64A-28BDDAFBDE32 wds:Q35903246-615AD470-AC97-4056-96CF-3B6ADA984F37 wds:Q34361292-6743A0AB-939E-40F4-8B81-BBF24DA77FD1 wds:Q35231737-6C35731D-23F2-45BE-A4B3-1B0C7FA5896A wds:Q35231757-FBAAB2B2-AD47-4080-BD43-E1392DC67A07 wds:Q92799075-C5BCB455-867D-4303-B35B-A05CFB312585 wds:Q35685503-CD738450-5334-4CDD-952D-1B2811F9A61D wds:Q33870886-61E7F704-E2BB-4E4F-898C-FE9DC4403FE2

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