Alpha, Beta- Unsaturated Lactone-Nitrone Cycloadditions: a Route to the Synthesis of (±)–Tussilagin
Reaction of nitrone (V with a, f1 -unsaturated lactone C.4) resulted in the isolation of a single adduct (7). The observed high regiochemical control has encouraged further explorations of natural product synthesis. A route to the synthesis of an interesting member of Pyrrolizidine- Alkaloid family;...
Saved in:
| Main Author: | |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
An-Najah National University
1994-09-01
|
| Series: | مجلة جامعة النجاح للأبحاث العلوم الطبيعية |
| Online Access: | https://journals.najah.edu/media/journals/full_texts/unsaturated-lactone-nitrone-cycloadditions-route-synthesis-tussilagin.pdf |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| _version_ | 1849339646252679168 |
|---|---|
| author | Mohammed A. Al-Nuri |
| author_facet | Mohammed A. Al-Nuri |
| author_sort | Mohammed A. Al-Nuri |
| collection | DOAJ |
| description | Reaction of nitrone (V with a, f1 -unsaturated lactone C.4) resulted in the isolation of a single adduct (7). The observed high regiochemical control has encouraged further explorations of natural product synthesis. A route to the synthesis of an interesting member of Pyrrolizidine- Alkaloid family; (±) -Tussilagin 90/ has been described. |
| format | Article |
| id | doaj-art-c5fb9b0b73a345e9bcc57a51b9a7b16a |
| institution | Kabale University |
| issn | 1727-2114 2311-8865 |
| language | English |
| publishDate | 1994-09-01 |
| publisher | An-Najah National University |
| record_format | Article |
| series | مجلة جامعة النجاح للأبحاث العلوم الطبيعية |
| spelling | doaj-art-c5fb9b0b73a345e9bcc57a51b9a7b16a2025-08-20T03:44:04ZengAn-Najah National Universityمجلة جامعة النجاح للأبحاث العلوم الطبيعية1727-21142311-88651994-09-0181496110.35552/anujr.a.8.1.425Alpha, Beta- Unsaturated Lactone-Nitrone Cycloadditions: a Route to the Synthesis of (±)–TussilaginMohammed A. Al-Nuri0NoneReaction of nitrone (V with a, f1 -unsaturated lactone C.4) resulted in the isolation of a single adduct (7). The observed high regiochemical control has encouraged further explorations of natural product synthesis. A route to the synthesis of an interesting member of Pyrrolizidine- Alkaloid family; (±) -Tussilagin 90/ has been described.https://journals.najah.edu/media/journals/full_texts/unsaturated-lactone-nitrone-cycloadditions-route-synthesis-tussilagin.pdf |
| spellingShingle | Mohammed A. Al-Nuri Alpha, Beta- Unsaturated Lactone-Nitrone Cycloadditions: a Route to the Synthesis of (±)–Tussilagin مجلة جامعة النجاح للأبحاث العلوم الطبيعية |
| title | Alpha, Beta- Unsaturated Lactone-Nitrone Cycloadditions: a Route to the Synthesis of (±)–Tussilagin |
| title_full | Alpha, Beta- Unsaturated Lactone-Nitrone Cycloadditions: a Route to the Synthesis of (±)–Tussilagin |
| title_fullStr | Alpha, Beta- Unsaturated Lactone-Nitrone Cycloadditions: a Route to the Synthesis of (±)–Tussilagin |
| title_full_unstemmed | Alpha, Beta- Unsaturated Lactone-Nitrone Cycloadditions: a Route to the Synthesis of (±)–Tussilagin |
| title_short | Alpha, Beta- Unsaturated Lactone-Nitrone Cycloadditions: a Route to the Synthesis of (±)–Tussilagin |
| title_sort | alpha beta unsaturated lactone nitrone cycloadditions a route to the synthesis of tussilagin |
| url | https://journals.najah.edu/media/journals/full_texts/unsaturated-lactone-nitrone-cycloadditions-route-synthesis-tussilagin.pdf |
| work_keys_str_mv | AT mohammedaalnuri alphabetaunsaturatedlactonenitronecycloadditionsaroutetothesynthesisoftussilagin |