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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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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. |
format | Online Article Text |
id | pubmed-6321290 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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