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Akademický článek

Bi(OTf) 3 -Catalyzed Cascade Cycloaddition-Decarbonylation- N -Deoxygenative Aromatization between 2-Arylisatogens and Styrenes: Unveiling a Synthesis of 2,4-Diarylquinolines.

Autor: Punjajom K; Program on Chemical Sciences, Chulabhorn Graduate Institute, 54 Kamphaeng Phet 6 Laksi, Bangkok, 10210, Thailand., Chonradeenitchakul S; Program on Chemical Sciences, Chulabhorn Graduate Institute, 54 Kamphaeng Phet 6 Laksi, Bangkok, 10210, Thailand., Tummatorn J; Laboratory of Medicinal Chemistry, Chulabhorn Research Institute, 54 Kamphaeng Phet 6 Laksi, Bangkok, 10210, Thailand.; Program on Chemical Sciences, Chulabhorn Graduate Institute, 54 Kamphaeng Phet 6 Laksi, Bangkok, 10210, Thailand.; Center of Excellence on Environmental Health and Toxicology (EHT), OPS, MHESI, Bangkok, 10400, Thailand., Ruchirawat S; Laboratory of Medicinal Chemistry, Chulabhorn Research Institute, 54 Kamphaeng Phet 6 Laksi, Bangkok, 10210, Thailand.; Program on Chemical Sciences, Chulabhorn Graduate Institute, 54 Kamphaeng Phet 6 Laksi, Bangkok, 10210, Thailand.; Center of Excellence on Environmental Health and Toxicology (EHT), OPS, MHESI, Bangkok, 10400, Thailand., Thongsornkleeb C; Laboratory of Medicinal Chemistry, Chulabhorn Research Institute, 54 Kamphaeng Phet 6 Laksi, Bangkok, 10210, Thailand.; Program on Chemical Sciences, Chulabhorn Graduate Institute, 54 Kamphaeng Phet 6 Laksi, Bangkok, 10210, Thailand.; Center of Excellence on Environmental Health and Toxicology (EHT), OPS, MHESI, Bangkok, 10400, Thailand.

Publikováno v: Organic letters [Org Lett] 2024 Nov 29; Vol. 26 (47), pp. 10066-10071. Date of Electronic Publication: 2024 Nov 15.

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Correction: Convergent synthesis of thiodiazole dioxides from simple ketones and amines through an unusual nitrogen-migration mechanism.

Autor: Punjajom K; Department of Chemistry, University of California Berkeley CA 94720 USA rsarpong@berkeley.edu., Sinclair PP; Department of Chemistry, University of California Berkeley CA 94720 USA rsarpong@berkeley.edu., Saha I; Janssen Research and Development San Diego California 92121 USA pgarciar@its.jnj.com terry.lebold@gmail.com., Seierstad M; Janssen Research and Development San Diego California 92121 USA pgarciar@its.jnj.com terry.lebold@gmail.com., Ameriks MK; Janssen Research and Development San Diego California 92121 USA pgarciar@its.jnj.com terry.lebold@gmail.com., García-Reynaga P; Janssen Research and Development San Diego California 92121 USA pgarciar@its.jnj.com terry.lebold@gmail.com., Lebold TP; Janssen Research and Development San Diego California 92121 USA pgarciar@its.jnj.com terry.lebold@gmail.com., Sarpong R; Department of Chemistry, University of California Berkeley CA 94720 USA rsarpong@berkeley.edu.

Publikováno v: Chemical science [Chem Sci] 2024 Jun 24; Vol. 15 (28), pp. 11145-11147. Date of Electronic Publication: 2024 Jun 24 (Print Publication: 2024).

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Akademický článek

Mn(OAc) 3 -Mediated One-Pot Condensation-Oxidative Annulation of 2-Alkynylanilines and 1,3-Ketoesters: Synthesis of 2-Substituted Quinolines.

Autor: Punjajom K; Program on Chemical Biology, Chulabhorn Graduate Institute, Center of Excellence on Environmental Health and Toxicology (EHT), Ministry of Education, 54 Kamphaeng Phet 6, Laksi, Bangkok 10210, Thailand., Ruengsangtongkul S; Laboratory of Medicinal Chemistry, Chulabhorn Research Institute, 54 Kamphaeng Phet 6, Laksi, Bangkok 10210, Thailand., Tummatorn J; Laboratory of Medicinal Chemistry, Chulabhorn Research Institute, 54 Kamphaeng Phet 6, Laksi, Bangkok 10210, Thailand.; Program on Chemical Biology, Chulabhorn Graduate Institute, Center of Excellence on Environmental Health and Toxicology (EHT), Ministry of Education, 54 Kamphaeng Phet 6, Laksi, Bangkok 10210, Thailand., Paiboonsombat P; Program on Chemical Biology, Chulabhorn Graduate Institute, Center of Excellence on Environmental Health and Toxicology (EHT), Ministry of Education, 54 Kamphaeng Phet 6, Laksi, Bangkok 10210, Thailand., Ruchirawat S; Laboratory of Medicinal Chemistry, Chulabhorn Research Institute, 54 Kamphaeng Phet 6, Laksi, Bangkok 10210, Thailand.; Program on Chemical Biology, Chulabhorn Graduate Institute, Center of Excellence on Environmental Health and Toxicology (EHT), Ministry of Education, 54 Kamphaeng Phet 6, Laksi, Bangkok 10210, Thailand., Thongsornkleeb C; Laboratory of Medicinal Chemistry, Chulabhorn Research Institute, 54 Kamphaeng Phet 6, Laksi, Bangkok 10210, Thailand.; Program on Chemical Biology, Chulabhorn Graduate Institute, Center of Excellence on Environmental Health and Toxicology (EHT), Ministry of Education, 54 Kamphaeng Phet 6, Laksi, Bangkok 10210, Thailand.

Publikováno v: The Journal of organic chemistry [J Org Chem] 2023 Jun 02; Vol. 88 (11), pp. 6736-6749. Date of Electronic Publication: 2023 May 04.

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Akademický článek

Chemoselective Synthesis of 1,1-Disubstituted Vinyl Triflates from Terminal Alkynes Using TfOH in the Presence of TMSN 3 .

Autor: Tummatorn J; Laboratory of Medicinal Chemistry , Chulabhorn Research Institute , 54 Kamphaeng Phet 6 , Laksi, Bangkok 10210 , Thailand.; Program on Chemical Biology , Chulabhorn Graduate Institute, Center of Excellence on Environmental Health and Toxicology (EHT), Ministry of Education , 54 Kamphaeng Phet 6 , Laksi, Bangkok 10210 , Thailand., Punjajom K; Program on Chemical Biology , Chulabhorn Graduate Institute, Center of Excellence on Environmental Health and Toxicology (EHT), Ministry of Education , 54 Kamphaeng Phet 6 , Laksi, Bangkok 10210 , Thailand., Rodphon W; Program on Chemical Biology , Chulabhorn Graduate Institute, Center of Excellence on Environmental Health and Toxicology (EHT), Ministry of Education , 54 Kamphaeng Phet 6 , Laksi, Bangkok 10210 , Thailand., Ruengsangtongkul S; Laboratory of Medicinal Chemistry , Chulabhorn Research Institute , 54 Kamphaeng Phet 6 , Laksi, Bangkok 10210 , Thailand., Chaisan N; Program on Chemical Biology , Chulabhorn Graduate Institute, Center of Excellence on Environmental Health and Toxicology (EHT), Ministry of Education , 54 Kamphaeng Phet 6 , Laksi, Bangkok 10210 , Thailand., Lumyong K; Laboratory of Medicinal Chemistry , Chulabhorn Research Institute , 54 Kamphaeng Phet 6 , Laksi, Bangkok 10210 , Thailand., Thongsornkleeb C; Laboratory of Organic Synthesis , Chulabhorn Research Institute , 54 Kamphaeng Phet 6 , Laksi, Bangkok 10210 , Thailand.; Program on Chemical Biology , Chulabhorn Graduate Institute, Center of Excellence on Environmental Health and Toxicology (EHT), Ministry of Education , 54 Kamphaeng Phet 6 , Laksi, Bangkok 10210 , Thailand., Nimnual P; Program on Chemical Biology , Chulabhorn Graduate Institute, Center of Excellence on Environmental Health and Toxicology (EHT), Ministry of Education , 54 Kamphaeng Phet 6 , Laksi, Bangkok 10210 , Thailand., Ruchirawat S; Laboratory of Medicinal Chemistry , Chulabhorn Research Institute , 54 Kamphaeng Phet 6 , Laksi, Bangkok 10210 , Thailand.; Program on Chemical Biology , Chulabhorn Graduate Institute, Center of Excellence on Environmental Health and Toxicology (EHT), Ministry of Education , 54 Kamphaeng Phet 6 , Laksi, Bangkok 10210 , Thailand.

Publikováno v: Organic letters [Org Lett] 2019 Jun 21; Vol. 21 (12), pp. 4694-4697. Date of Electronic Publication: 2019 Jun 11.

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