About: New C=C bond formation via nonstoichiometric titanium(IV) halide mediated vicinal difunctionalization of alpha,beta-unsaturated acyclic ketones

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About: New C=C bond formation via nonstoichiometric titanium(IV) halide mediated vicinal difunctionalization of alpha,beta-unsaturated acyclic ketones Goto Sponge NotDistinct Permalink

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scientific article published on 01 March 2000

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) wüsseschaftlicher Artikel, wo im März 2000 veröffentlicht worden isch (gsw) im März 2000 veröffentlichter wissenschaftlicher Artikel (de) наукова стаття, опублікована в березні 2000 (uk) artículu científicu espublizáu en marzu de 2000 (ast) scientific article published on 01 March 2000 (en)
publication date	wds:Q73799890-264D21B0-DA24-4042-BA76-C8070CE5644C
publication date	2000-03-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q73799890-3F61B280-8492-49D6-9F93-E1F9582AC848 wds:Q73799890-78A8CB86-A747-4B7D-8D37-CED58C8DEE13 wds:Q73799890-7BF95B11-99EA-45B5-ADB2-FB2D5EB6E472 wds:Q73799890-F2ABFD14-5C44-4816-BF1E-558A3045A7B9
author name string	Li G Gao J Enright M Wei HX
rdfs:label	New C=C bond formation via nonstoichiometric titanium(IV) halide mediated vicinal difunctionalization of alpha,beta-unsaturated acyclic ketones (en) New C=C bond formation via nonstoichiometric titanium(IV) halide mediated vicinal difunctionalization of alpha,beta-unsaturated acyclic ketones (nl)
skos:prefLabel	New C=C bond formation via nonstoichiometric titanium(IV) halide mediated vicinal difunctionalization of alpha,beta-unsaturated acyclic ketones (en) New C=C bond formation via nonstoichiometric titanium(IV) halide mediated vicinal difunctionalization of alpha,beta-unsaturated acyclic ketones (nl)
name	New C=C bond formation via nonstoichiometric titanium(IV) halide mediated vicinal difunctionalization of alpha,beta-unsaturated acyclic ketones (en) New C=C bond formation via nonstoichiometric titanium(IV) halide mediated vicinal difunctionalization of alpha,beta-unsaturated acyclic ketones (nl)
title	wds:Q73799890-AD1DB1ED-3242-4F69-BB61-3959C30CFFDD
title	New C=C bond formation via nonstoichiometric titanium(IV) halide mediated vicinal difunctionalization of alpha,beta-unsaturated acyclic ketones (en)
page(s)	wds:Q73799890-CB54EA58-FA18-42BA-8BD4-D0AA4545007F
page(s)	617-620
instance of	wds:Q73799890-8F2BBDE3-FFB1-486B-9710-8AC87DA26532
instance of	scholarly article
main subject	wds:Q73799890-8E9A036A-3365-4BB0-899F-14F557932124
main subject	titanium
PubMed ID	wds:Q73799890-826CDC44-97C8-4EAA-BD1B-1848FBA1EED0
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/10814392
PubMed ID	10814392
published in	wds:Q73799890-C3449F86-8A84-4033-B666-67EDBD955D6B
published in	Organic Letters
issue	wds:Q73799890-43CDC603-37E4-46A7-BD06-012BD0FB58B7
volume	wds:Q73799890-9339AE0D-1591-4CC1-B539-B398E26B37F1
issue	5
volume	2
DOI	wds:Q73799890-C3FA1D3E-05BB-46B4-B511-768A43A1F21B
DOI	http://dx.doi.org/10.1021/OL9904040
DOI	10.1021/OL9904040
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q73799890
is cites work of	Formation of 13C-, 15N-, and 18O-Labeled Guanidinohydantoin from Guanosine Oxidation with Singlet Oxygen. Implications for Structure and Mechanism Enantiospecific total synthesis of the hapalindoles, fischerindoles, and welwitindolinones via a redox economic approach Lewis acid-promoted Baylis-Hillman-type reaction of alpha,beta-unsaturated ethyl thioester with aldehydes without the use of a Lewis base. The Baylis-Hillman condensation of alpha,beta-conjugate cycloketones with aldehydes using diethylaluminum iodide alone as the promoter A novel, tandem construction of C-N and C-C bonds: facile and one-pot transformation of the Baylis-Hillman adducts into 2-benzazepines Different Reaction Patterns in the Reaction of Aryl Aldehydes with Phenyl Vinyl Ketone, Phenyl Acrylate and Phenyl Thioacrylate A Highly Active and Selective Catalyst System for the Baylis–Hillman Reaction Three-Component Halo Aldol Condensation of Thioacrylates with Aldehydes Mediated by Titanium (IV) Halide† Amine and Titanium (IV) Chloride, Boron (III) Chloride or Zirconium (IV) Chloride-Promoted Baylis-Hillman Reactions
is cites work of	wds:Q94089163-3F640FD4-A755-4AED-A3BF-782F68A402E5 wds:Q37080286-51EAA123-F6F9-425A-9F0D-EF0A7F9756E0 wds:Q78511181-DDD6B15C-FC5E-4BAD-82E9-C8A3DEE7120D wds:Q79243576-02808EF2-8191-4924-A0E3-19360D794028 wds:Q94089119-E7BAD5EF-507A-4130-89F6-BA5D91823E4E wds:Q54318721-2C2DFBF5-C616-44E6-8683-CBA0714EA3C0 wds:Q94158278-6689622E-176C-4CEC-826D-8E263D290744 wds:Q30883974-F326A833-BF71-487C-8C18-28CDD110001B wds:Q44737607-AECC6C1F-8858-487F-B5D4-BDE35E056530

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