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Applications of C–H Functionalization Logic to Cyclobutane Synthesis
[Image: see text] The application of C–H functionalization logic to target-oriented synthesis provides an exciting new venue for the development of new and useful strategies in organic chemistry. In this article, C–H functionalization reactions are explored as an alternative approach to access pseud...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3985916/ https://www.ncbi.nlm.nih.gov/pubmed/24548142 http://dx.doi.org/10.1021/jo4027148 |
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author | Gutekunst, Will R. Baran, Phil S. |
author_facet | Gutekunst, Will R. Baran, Phil S. |
author_sort | Gutekunst, Will R. |
collection | PubMed |
description | [Image: see text] The application of C–H functionalization logic to target-oriented synthesis provides an exciting new venue for the development of new and useful strategies in organic chemistry. In this article, C–H functionalization reactions are explored as an alternative approach to access pseudodimeric cyclobutane natural products, such as the dictazole and the piperarborenine families. The use of these strategies in a variety of complex settings highlights the subtle geometric, steric, and electronic effects at play in the auxiliary guided C–H functionalization of cyclobutanes. |
format | Online Article Text |
id | pubmed-3985916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-39859162015-02-18 Applications of C–H Functionalization Logic to Cyclobutane Synthesis Gutekunst, Will R. Baran, Phil S. J Org Chem [Image: see text] The application of C–H functionalization logic to target-oriented synthesis provides an exciting new venue for the development of new and useful strategies in organic chemistry. In this article, C–H functionalization reactions are explored as an alternative approach to access pseudodimeric cyclobutane natural products, such as the dictazole and the piperarborenine families. The use of these strategies in a variety of complex settings highlights the subtle geometric, steric, and electronic effects at play in the auxiliary guided C–H functionalization of cyclobutanes. American Chemical Society 2014-02-18 2014-03-21 /pmc/articles/PMC3985916/ /pubmed/24548142 http://dx.doi.org/10.1021/jo4027148 Text en Copyright © 2014 American Chemical Society |
spellingShingle | Gutekunst, Will R. Baran, Phil S. Applications of C–H Functionalization Logic to Cyclobutane Synthesis |
title | Applications of C–H
Functionalization Logic
to Cyclobutane Synthesis |
title_full | Applications of C–H
Functionalization Logic
to Cyclobutane Synthesis |
title_fullStr | Applications of C–H
Functionalization Logic
to Cyclobutane Synthesis |
title_full_unstemmed | Applications of C–H
Functionalization Logic
to Cyclobutane Synthesis |
title_short | Applications of C–H
Functionalization Logic
to Cyclobutane Synthesis |
title_sort | applications of c–h
functionalization logic
to cyclobutane synthesis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3985916/ https://www.ncbi.nlm.nih.gov/pubmed/24548142 http://dx.doi.org/10.1021/jo4027148 |
work_keys_str_mv | AT gutekunstwillr applicationsofchfunctionalizationlogictocyclobutanesynthesis AT baranphils applicationsofchfunctionalizationlogictocyclobutanesynthesis |