About: Microwave-Assisted One-Pot Tandem Reactions for Direct Conversion of Primary Alcohols and Aldehydes to Triazines and Tetrazoles in Aqueous Media

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About: Microwave-Assisted One-Pot Tandem Reactions for Direct Conversion of Primary Alcohols and Aldehydes to Triazines and Tetrazoles in Aqueous Media Goto Sponge NotDistinct Permalink

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scientific article published on 16 March 2007

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у квітні 2007 (uk) article scientifique publié en 2007 (fr) im April 2007 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 16 March 2007 (en) artículu científicu espublizáu en marzu de 2007 (ast)
publication date	wds:Q58239619-A9F2CE2C-1D6F-46B2-B571-E9C8076F47A1
publication date	2007-03-16 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q58239619-400F03FB-1D1A-416C-BF49-32338FC8A031
language of work or name	English
cites work	wds:Q58239619-F9872BB8-2A73-46AE-90E4-D4929E53D849
cites work	Chemistry in living systems
author name string	wds:Q58239619-13602E0D-F520-4A6C-86C2-BB45F36D8EDB wds:Q58239619-D930A43E-F936-45B5-8B93-9CC86FAE5212
author name string	Jim-Min Fang Jiun-Jie Shie
rdfs:label	Microwave-Assisted One-Pot Tandem Reactions for Direct Conversion of Primary Alcohols and Aldehydes to Triazines and Tetrazoles in Aqueous Media (en) Microwave-Assisted One-Pot Tandem Reactions for Direct Conversion of Primary Alcohols and Aldehydes to Triazines and Tetrazoles in Aqueous Media (nl)
skos:prefLabel	Microwave-Assisted One-Pot Tandem Reactions for Direct Conversion of Primary Alcohols and Aldehydes to Triazines and Tetrazoles in Aqueous Media (en) Microwave-Assisted One-Pot Tandem Reactions for Direct Conversion of Primary Alcohols and Aldehydes to Triazines and Tetrazoles in Aqueous Media (nl)
name	Microwave-Assisted One-Pot Tandem Reactions for Direct Conversion of Primary Alcohols and Aldehydes to Triazines and Tetrazoles in Aqueous Media (en) Microwave-Assisted One-Pot Tandem Reactions for Direct Conversion of Primary Alcohols and Aldehydes to Triazines and Tetrazoles in Aqueous Media (nl)
author	wds:Q58239619-35A1C3AF-0930-4828-BB89-079AB7F1B513 wds:Q58239619-AD7BEECB-4799-4170-89AA-3C1E1F0BF271
author	Jim-Min Fang Jiun-Jie Shie
title	wds:Q58239619-3BE50CA1-1B3E-44B1-99E4-B9CD09329FDE
title	Microwave-assisted one-pot tandem reactions for direct conversion of primary alcohols and aldehydes to triazines and tetrazoles in aqueous media (en)
page(s)	wds:Q58239619-CD9A9DCC-CF38-4B1B-B556-60B6728AB91A
page(s)	3141-3144
instance of	wds:Q58239619-A35D1B56-2C74-4AAC-9388-B878E7B7C371
instance of	scholarly article
main subject	wds:Q58239619-7CEC7E38-2CF6-4AB7-A5E1-8F4E47B74895
main subject	microwave
PubMed ID	wds:Q58239619-F3B4C10D-1D52-49E6-9FF5-4380EC86D6E8
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17362044
PubMed ID	17362044
published in	wds:Q58239619-3855B14F-9548-468D-A060-5A62C2796E3A
published in	Journal of Organic Chemistry
issue	wds:Q58239619-77CE7B73-78BF-4AEB-919D-E4EC332BC356
volume	wds:Q58239619-5422D4F6-1766-4C6D-9E09-96A70F89E72D
issue	8
volume	72
DOI	wds:Q58239619-7A51B11E-8B01-4BBC-A290-2C9E45BBB5EE
DOI	http://dx.doi.org/10.1021/JO0625352
DOI	10.1021/JO0625352
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q58239619
is cites work of	Transition metal-mediated synthesis of monocyclic aromatic heterocycles Tandem inverse-electron-demand hetero-/retro-Diels-Alder reactions for aromatic nitrogen heterocycle synthesis Alternative energy input: mechanochemical, microwave and ultrasound-assisted organic synthesis A Convenient, TiCl 4 /SnCl 4 -Mediated Synthesis of N-Phenyl or N-Aryl Benzamidines and N-Phenylpicolinamidines Controlled microwave heating in modern organic synthesis: highlights from the 2004-2008 literature. Steroid/triterpenoid functional molecules based on "click chemistry". A Synthetic Route Toward Tetrazoles: The Thermolysis of Geminal Diazides Microwave-Assisted Synthesis of Bioactive Six-Membered Heterocycles and Their Fused Analogues Regioselective, unconventional Pictet-Spengler cyclization strategy toward the synthesis of benzimidazole-linked imidazoquinoxalines on a soluble polymer support. Aminoazole-Based Diversity-Oriented Synthesis of Heterocycles Syntheses of 2-substituted 1-amino-4-bromoanthraquinones (bromaminic acid analogues) - precursors for dyes and drugs. Sustainable Generation of Ni(OH)2 Nanoparticles for the Green Synthesis of 5-Substituted 1H-Tetrazoles: A Competent Turn on Fluorescence Sensing of H2O2
is cites work of	wds:Q42108528-7E58876F-DEA6-4620-8904-E08AA00469E3 wds:Q92588697-54917FA1-E7D2-45E8-BE46-A5E428ADC60D wds:Q37955087-2A583516-DD08-4797-91FF-F0543C04098F wds:Q38053278-12DF7589-5F02-45F0-B11B-D50C0DA36FAF wds:Q53255547-AECC2437-E5DB-451E-BE18-4CCC489EC850 wds:Q59808480-46B8056E-1F9C-48F5-8471-5A18173EAD5F wds:Q92938147-18AF9A1B-2B3F-4655-A82A-F1FD0A6BA3F2 wds:Q26752782-C35D54C9-70AB-42D7-B460-C49BE0483489 wds:Q36831938-72AD3B8F-5E97-46FE-969F-9E3674CDCB3C wds:Q37925686-7F049B24-E12F-4506-BD8B-1E383719CCBB wds:Q41952614-F6F6811B-E299-4FF3-890A-745A2FC7ACA2 wds:Q37453136-DB22DC24-AD8A-4F1D-885E-9C39879665F0

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