Jesse Teske

Works (5)

Updated: July 5th, 2023 15:54

2009 article

Open-Vessel Microwave-Mediated [2+2+2]-Cyclotrimerization Reactions

Deiters, A., Young, D., & Teske, J. (2009, October 7). Synthesis.

By: A. Deiters*, D. Young* & J. Teske*

author keywords: [2+2+2] cyclotrimerization; alkynes; microwave; bicyclic compounds; transition metal catalysis
topics (OpenAlex): Catalytic Alkyne Reactions; Catalysis for Biomass Conversion
Source: Web Of Science
Added: August 6, 2018

2008 article

A Cyclotrimerization Route to Cannabinoids

Teske, J. A., & Deiters, A. (2008, May 2). Organic Letters.

By: J. Teske n & A. Deiters n

MeSH headings : Alkynes / chemistry; Cannabinoids / chemical synthesis; Cannabinoids / chemistry; Cyclization; Nitriles / chemistry
topics (OpenAlex): Cannabis and Cannabinoid Research; Synthesis of Indole Derivatives; Chemical synthesis and alkaloids
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Source: Web Of Science
Added: August 6, 2018

2007 article

Microwave-Mediated Nickel-Catalyzed Cyclotrimerization Reactions:  Total Synthesis of Illudinine

Teske, J. A., & Deiters, A. (2007, December 5). The Journal of Organic Chemistry.

By: J. Teske n & A. Deiters n

MeSH headings : Catalysis; Cyclization; Microwaves; Molecular Structure; Nickel / chemistry; Nickel / radiation effects; Organometallic Compounds / chemistry; Organometallic Compounds / radiation effects; Sesquiterpenes / chemical synthesis; Sesquiterpenes / chemistry; Sesquiterpenes / radiation effects; Stereoisomerism
topics (OpenAlex): Multicomponent Synthesis of Heterocycles; Microwave-Assisted Synthesis and Applications; Synthesis and Biological Evaluation
TL;DR: The developed microwave-mediated Ni-catalyzed cyclotrimerization reaction was employed as the key step in a concise synthesis of the isoquinoline natural product illudinine, the first example of a Ni-Catalyzedcyclotriming reaction in total synthesis. (via Semantic Scholar)
Source: Web Of Science
Added: August 6, 2018

2007 article

Phenanthridine synthesis via [2+2+2] cyclotrimerization reactions

Sripada, L., Teske, J. A., & Deiters, A. (2007, December 3). Organic & Biomolecular Chemistry.

By: L. Sripada n, J. Teske n & A. Deiters n

MeSH headings : Cyclization; Microwaves; Molecular Structure; Phenanthridines / chemical synthesis; Phenanthridines / chemistry; Phenanthridines / radiation effects; Stereoisomerism
topics (OpenAlex): Chemical synthesis and alkaloids; Cyclopropane Reaction Mechanisms
TL;DR: A concise synthesis of phenanthridines via a microwave-assisted [2+2+3+2] cyclotrimerization reaction has been developed and is applicable to selective separation of Na6(CO3)(SO4)2, Na2CO3, and Na2SO4 from Na3SO4-based polymers. (via Semantic Scholar)
Source: Web Of Science
Added: August 6, 2018

2007 article

Synthesis of Indanones via Solid-Supported [2+2+2] Cyclotrimerization

Senaiar, R. S., Teske, J. A., Young, D. D., & Deiters, A. (2007, September 1). The Journal of Organic Chemistry.

By: R. Senaiar n, J. Teske n, D. Young n & A. Deiters n

topics (OpenAlex): Synthesis and biological activity; Synthesis of Indole Derivatives; Synthesis of Organic Compounds
TL;DR: A new facile approach toward natural and unnatural indanones has been developed, featuring a solid-supported [2+2+3+2] cyclotrimerization as the key step. (via Semantic Scholar)
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Source: Web Of Science
Added: August 6, 2018

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