Cargando…
Enantioselective synthesis of polyhydroxyindolizidinone and quinolizidinone derivatives from a common precursor
A concise asymmetric synthetic route to two new tetrahydroxyindolizidinone and quinolizidinone derivatives has been developed from a common intermediate which featured a highly selective dihydroxylation reaction and a RCM reaction as key steps.
| Autores principales: | , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Beilstein-Institut
2014
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4311665/ https://www.ncbi.nlm.nih.gov/pubmed/25670979 http://dx.doi.org/10.3762/bjoc.10.327 |
| _version_ | 1782355037038575616 |
|---|---|
| author | Saha, Nemai Chattopadhyay, Shital K |
| author_facet | Saha, Nemai Chattopadhyay, Shital K |
| author_sort | Saha, Nemai |
| collection | PubMed |
| description | A concise asymmetric synthetic route to two new tetrahydroxyindolizidinone and quinolizidinone derivatives has been developed from a common intermediate which featured a highly selective dihydroxylation reaction and a RCM reaction as key steps. |
| format | Online Article Text |
| id | pubmed-4311665 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2014 |
| publisher | Beilstein-Institut |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-43116652015-02-10 Enantioselective synthesis of polyhydroxyindolizidinone and quinolizidinone derivatives from a common precursor Saha, Nemai Chattopadhyay, Shital K Beilstein J Org Chem Full Research Paper A concise asymmetric synthetic route to two new tetrahydroxyindolizidinone and quinolizidinone derivatives has been developed from a common intermediate which featured a highly selective dihydroxylation reaction and a RCM reaction as key steps. Beilstein-Institut 2014-12-22 /pmc/articles/PMC4311665/ /pubmed/25670979 http://dx.doi.org/10.3762/bjoc.10.327 Text en Copyright © 2014, Saha and Chattopadhyay https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
| spellingShingle | Full Research Paper Saha, Nemai Chattopadhyay, Shital K Enantioselective synthesis of polyhydroxyindolizidinone and quinolizidinone derivatives from a common precursor |
| title | Enantioselective synthesis of polyhydroxyindolizidinone and quinolizidinone derivatives from a common precursor |
| title_full | Enantioselective synthesis of polyhydroxyindolizidinone and quinolizidinone derivatives from a common precursor |
| title_fullStr | Enantioselective synthesis of polyhydroxyindolizidinone and quinolizidinone derivatives from a common precursor |
| title_full_unstemmed | Enantioselective synthesis of polyhydroxyindolizidinone and quinolizidinone derivatives from a common precursor |
| title_short | Enantioselective synthesis of polyhydroxyindolizidinone and quinolizidinone derivatives from a common precursor |
| title_sort | enantioselective synthesis of polyhydroxyindolizidinone and quinolizidinone derivatives from a common precursor |
| topic | Full Research Paper |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4311665/ https://www.ncbi.nlm.nih.gov/pubmed/25670979 http://dx.doi.org/10.3762/bjoc.10.327 |
| work_keys_str_mv | AT sahanemai enantioselectivesynthesisofpolyhydroxyindolizidinoneandquinolizidinonederivativesfromacommonprecursor AT chattopadhyayshitalk enantioselectivesynthesisofpolyhydroxyindolizidinoneandquinolizidinonederivativesfromacommonprecursor |