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DDQ-Promoted Mild and Efficient Metal-Free Oxidative α-Cyanation of N-Acyl/Sulfonyl 1,2,3,4-Tetrahydroisoquinolines

A mild and highly efficient metal-free oxidative α-cyanation of N-acyl/sulfonyl 1,2,3,4-tetrahydroisoquinolines (THIQs) has been accomplished at an ambient temperature via DDQ oxidation and subsequent trapping of N-acyl/sulfonyl iminium ions with (n-Bu)(3)SnCN. Employing readily removable N-acyl/sul...

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Detalles Bibliográficos
Autores principales: Kim, Hong Pyo, Yu, Heesun, Kim, Hyoungsu, Kim, Seok-Ho, Lee, Dongjoo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6321290/
https://www.ncbi.nlm.nih.gov/pubmed/30563272
http://dx.doi.org/10.3390/molecules23123223
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author Kim, Hong Pyo
Yu, Heesun
Kim, Hyoungsu
Kim, Seok-Ho
Lee, Dongjoo
author_facet Kim, Hong Pyo
Yu, Heesun
Kim, Hyoungsu
Kim, Seok-Ho
Lee, Dongjoo
author_sort Kim, Hong Pyo
collection PubMed
description A mild and highly efficient metal-free oxidative α-cyanation of N-acyl/sulfonyl 1,2,3,4-tetrahydroisoquinolines (THIQs) has been accomplished at an ambient temperature via DDQ oxidation and subsequent trapping of N-acyl/sulfonyl iminium ions with (n-Bu)(3)SnCN. Employing readily removable N-acyl/sulfonyl groups as protecting groups rather than N-aryl ones enables a wide range of applications in natural product synthesis. The synthetic utility of the method was illustrated using a short and efficient formal total synthesis of (±)-calycotomine in three steps.
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spelling pubmed-63212902019-01-14 DDQ-Promoted Mild and Efficient Metal-Free Oxidative α-Cyanation of N-Acyl/Sulfonyl 1,2,3,4-Tetrahydroisoquinolines Kim, Hong Pyo Yu, Heesun Kim, Hyoungsu Kim, Seok-Ho Lee, Dongjoo Molecules Article A mild and highly efficient metal-free oxidative α-cyanation of N-acyl/sulfonyl 1,2,3,4-tetrahydroisoquinolines (THIQs) has been accomplished at an ambient temperature via DDQ oxidation and subsequent trapping of N-acyl/sulfonyl iminium ions with (n-Bu)(3)SnCN. Employing readily removable N-acyl/sulfonyl groups as protecting groups rather than N-aryl ones enables a wide range of applications in natural product synthesis. The synthetic utility of the method was illustrated using a short and efficient formal total synthesis of (±)-calycotomine in three steps. MDPI 2018-12-06 /pmc/articles/PMC6321290/ /pubmed/30563272 http://dx.doi.org/10.3390/molecules23123223 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kim, Hong Pyo
Yu, Heesun
Kim, Hyoungsu
Kim, Seok-Ho
Lee, Dongjoo
DDQ-Promoted Mild and Efficient Metal-Free Oxidative α-Cyanation of N-Acyl/Sulfonyl 1,2,3,4-Tetrahydroisoquinolines
title DDQ-Promoted Mild and Efficient Metal-Free Oxidative α-Cyanation of N-Acyl/Sulfonyl 1,2,3,4-Tetrahydroisoquinolines
title_full DDQ-Promoted Mild and Efficient Metal-Free Oxidative α-Cyanation of N-Acyl/Sulfonyl 1,2,3,4-Tetrahydroisoquinolines
title_fullStr DDQ-Promoted Mild and Efficient Metal-Free Oxidative α-Cyanation of N-Acyl/Sulfonyl 1,2,3,4-Tetrahydroisoquinolines
title_full_unstemmed DDQ-Promoted Mild and Efficient Metal-Free Oxidative α-Cyanation of N-Acyl/Sulfonyl 1,2,3,4-Tetrahydroisoquinolines
title_short DDQ-Promoted Mild and Efficient Metal-Free Oxidative α-Cyanation of N-Acyl/Sulfonyl 1,2,3,4-Tetrahydroisoquinolines
title_sort ddq-promoted mild and efficient metal-free oxidative α-cyanation of n-acyl/sulfonyl 1,2,3,4-tetrahydroisoquinolines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6321290/
https://www.ncbi.nlm.nih.gov/pubmed/30563272
http://dx.doi.org/10.3390/molecules23123223
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