The Total Synthesis of Racemic Teucvin and 12-epi-Teucvin
Complete face‐, stereo‐, and regioselectivity in the Diels–Alder reaction of compounds 1 and 2 was the key to the first total synthesis, in racemic form, of the 19‐norclerodane diterpenoids teucvin and 12‐epi‐teucvin.
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Veröffentlicht in: | Angewandte Chemie International Edition 2003-04, Vol.42 (16), p.1851-1853 |
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container_title | Angewandte Chemie International Edition |
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creator | Liu, Hsing-Jang Zhu, Jia-Liang Chen, I-Chia Jankowska, Renata Han, Yongxin Shia, Kak-Shan |
description | Complete face‐, stereo‐, and regioselectivity in the Diels–Alder reaction of compounds 1 and 2 was the key to the first total synthesis, in racemic form, of the 19‐norclerodane diterpenoids teucvin and 12‐epi‐teucvin. |
doi_str_mv | 10.1002/anie.200250681 |
format | Article |
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subjects | Diels-Alder reaction natural products terpenoids teucvin total synthesis |
title | The Total Synthesis of Racemic Teucvin and 12-epi-Teucvin |
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