Alpha, Beta- Unsaturated Lactone-Nitrone Cycloadditions: a Route to the Synthesis of (±)–Tussilagin
Authors:
Article info
49 - 61
Keywords
Abstract
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.
Al-Nuri, M. A. (1994). Alpha, Beta- Unsaturated Lactone-Nitrone Cycloadditions: a Route to the Synthesis of (±)–Tussilagin. An-Najah University Journal for Research - A (Natural Sciences), 8(1), 49–61. https://doi.org/10.35552/anujr.a.8.1.425
[1]M. A. Al-Nuri, “Alpha, Beta- Unsaturated Lactone-Nitrone Cycloadditions: a Route to the Synthesis of (±)–Tussilagin,” An-Najah University Journal for Research - A (Natural Sciences), vol. 8, no. 1, pp. 49–61, Jan. 1994, doi: 10.35552/anujr.a.8.1.425.
Al-Nuri, Mohammed A. “Alpha, Beta- Unsaturated Lactone-Nitrone Cycloadditions: A Route to the Synthesis of (±)–Tussilagin.” An-Najah University Journal for Research - A (Natural Sciences), vol. 8, no. 1, Jan. 1994, pp. 49–61. Crossref, https://doi.org/10.35552/anujr.a.8.1.425.
1.Al-Nuri MA. Alpha, Beta- Unsaturated Lactone-Nitrone Cycloadditions: a Route to the Synthesis of (±)–Tussilagin. An-Najah University Journal for Research - A (Natural Sciences) [Internet]. 1994 Jan;8(1):49–61. Available from: http://dx.doi.org/10.35552/anujr.a.8.1.425
Al-Nuri, Mohammed A. “Alpha, Beta- Unsaturated Lactone-Nitrone Cycloadditions: A Route to the Synthesis of (±)–Tussilagin.” An-Najah University Journal for Research - A (Natural Sciences) 8, no. 1 (January 1994): 49–61. https://doi.org/10.35552/anujr.a.8.1.425.
Alpha, Beta- Unsaturated Lactone-Nitrone Cycloadditions: a Route to the Synthesis of (±)–Tussilagin
المؤلفون:
معلومات المقال
49 - 61
الكلمات الإفتتاحية
الملخص
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.
Al-Nuri, M. A. (1994). Alpha, Beta- Unsaturated Lactone-Nitrone Cycloadditions: a Route to the Synthesis of (±)–Tussilagin. An-Najah University Journal for Research - A (Natural Sciences), 8(1), 49–61. https://doi.org/10.35552/anujr.a.8.1.425
[1]M. A. Al-Nuri, “Alpha, Beta- Unsaturated Lactone-Nitrone Cycloadditions: a Route to the Synthesis of (±)–Tussilagin,” An-Najah University Journal for Research - A (Natural Sciences), vol. 8, no. 1, pp. 49–61, Jan. 1994, doi: 10.35552/anujr.a.8.1.425.
Al-Nuri, Mohammed A. “Alpha, Beta- Unsaturated Lactone-Nitrone Cycloadditions: A Route to the Synthesis of (±)–Tussilagin.” An-Najah University Journal for Research - A (Natural Sciences), vol. 8, no. 1, Jan. 1994, pp. 49–61. Crossref, https://doi.org/10.35552/anujr.a.8.1.425.
1.Al-Nuri MA. Alpha, Beta- Unsaturated Lactone-Nitrone Cycloadditions: a Route to the Synthesis of (±)–Tussilagin. An-Najah University Journal for Research - A (Natural Sciences) [Internet]. 1994 Jan;8(1):49–61. Available from: http://dx.doi.org/10.35552/anujr.a.8.1.425
Al-Nuri, Mohammed A. “Alpha, Beta- Unsaturated Lactone-Nitrone Cycloadditions: A Route to the Synthesis of (±)–Tussilagin.” An-Najah University Journal for Research - A (Natural Sciences) 8, no. 1 (January 1994): 49–61. https://doi.org/10.35552/anujr.a.8.1.425.
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