Concise synthesis of the vasorelaxant alkaloids schwarzinicines A and B
A concise synthesis of the 1,4-diarylbutanoid-phenethylamine alkaloids, schwarzinicines A (1) and B (2), recently isolated from Ficus schwarzii, is reported. Key steps include a Claisen condensation to assemble the 1,4-diaryl-2-butanone intermediate, followed by a reductive amination to furnish the...
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my.um.eprints.418302023-10-20T04:48:32Z http://eprints.um.edu.my/41830/ Concise synthesis of the vasorelaxant alkaloids schwarzinicines A and B Lee, Fong-Kai Krishnan, Premanand Muhamad, Azira Low, Yun-Yee Kam, Toh-Seok Ting, Kang-Nee Lim, Kuan-Hon QD Chemistry A concise synthesis of the 1,4-diarylbutanoid-phenethylamine alkaloids, schwarzinicines A (1) and B (2), recently isolated from Ficus schwarzii, is reported. Key steps include a Claisen condensation to assemble the 1,4-diaryl-2-butanone intermediate, followed by a reductive amination to furnish the core skeleton of the target compounds. The overall synthetic yields of 1 and 2 were 9.1% and 3.5%, respectively. Synthetic (-)-1, (+)-1 and (+/-)-1 exhibited comparable vasorelaxation as natural schwarzinicine A on rat isolated aortic rings, suggesting that the observed vasorelaxant effects were not influenced by the chirality at C-2. Taylor & Francis 2022-08-01 Article PeerReviewed Lee, Fong-Kai and Krishnan, Premanand and Muhamad, Azira and Low, Yun-Yee and Kam, Toh-Seok and Ting, Kang-Nee and Lim, Kuan-Hon (2022) Concise synthesis of the vasorelaxant alkaloids schwarzinicines A and B. Natural Product Research, 36 (15). pp. 3972-3978. ISSN 1478-6419, DOI https://doi.org/10.1080/14786419.2021.1903005 <https://doi.org/10.1080/14786419.2021.1903005>. 10.1080/14786419.2021.1903005 |
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QD Chemistry Lee, Fong-Kai Krishnan, Premanand Muhamad, Azira Low, Yun-Yee Kam, Toh-Seok Ting, Kang-Nee Lim, Kuan-Hon Concise synthesis of the vasorelaxant alkaloids schwarzinicines A and B |
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A concise synthesis of the 1,4-diarylbutanoid-phenethylamine alkaloids, schwarzinicines A (1) and B (2), recently isolated from Ficus schwarzii, is reported. Key steps include a Claisen condensation to assemble the 1,4-diaryl-2-butanone intermediate, followed by a reductive amination to furnish the core skeleton of the target compounds. The overall synthetic yields of 1 and 2 were 9.1% and 3.5%, respectively. Synthetic (-)-1, (+)-1 and (+/-)-1 exhibited comparable vasorelaxation as natural schwarzinicine A on rat isolated aortic rings, suggesting that the observed vasorelaxant effects were not influenced by the chirality at C-2. |
format |
Article |
author |
Lee, Fong-Kai Krishnan, Premanand Muhamad, Azira Low, Yun-Yee Kam, Toh-Seok Ting, Kang-Nee Lim, Kuan-Hon |
author_facet |
Lee, Fong-Kai Krishnan, Premanand Muhamad, Azira Low, Yun-Yee Kam, Toh-Seok Ting, Kang-Nee Lim, Kuan-Hon |
author_sort |
Lee, Fong-Kai |
title |
Concise synthesis of the vasorelaxant alkaloids schwarzinicines A and B |
title_short |
Concise synthesis of the vasorelaxant alkaloids schwarzinicines A and B |
title_full |
Concise synthesis of the vasorelaxant alkaloids schwarzinicines A and B |
title_fullStr |
Concise synthesis of the vasorelaxant alkaloids schwarzinicines A and B |
title_full_unstemmed |
Concise synthesis of the vasorelaxant alkaloids schwarzinicines A and B |
title_sort |
concise synthesis of the vasorelaxant alkaloids schwarzinicines a and b |
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Taylor & Francis |
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2022 |
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http://eprints.um.edu.my/41830/ |
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1781704561596039168 |