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Studies on novel macrocyclization methods of cembrane-type diterpenoids: a Stille cyclization approach to (±)-isocembrene

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Title: Studies on novel macrocyclization methods of cembrane-type diterpenoids: a Stille cyclization approach to (±)-isocembrene
Authors: Peng, Lizeng1, Zhang, Fengzhi1, Mei, Tiansheng1, Zhang, Tao1, Li, Yulin liyl@lzu.edu.cn
Source: Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry. Jul2003, Vol. 44 Issue 31, p5921. 3p.
Subjects: Stille reaction, Asymmetric synthesis
Abstract: An efficient total synthesis of (±)-isocembrene via an intramolecular Stille cross-coupling reaction is described. A novel strategy towards the 1,3-diene-based cembrane-type macrocyclic diterpenoids has been realized. [Copyright &y& Elsevier]
Copyright of Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry is the property of Pergamon Press - An Imprint of Elsevier Science and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
Database: Engineering Source
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Header DbId: egs
DbLabel: Engineering Source
An: 10176761
AccessLevel: 6
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
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  Data: <searchLink fieldCode="AR" term="%22Peng%2C+Lizeng%22">Peng, Lizeng</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Zhang%2C+Fengzhi%22">Zhang, Fengzhi</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Mei%2C+Tiansheng%22">Mei, Tiansheng</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Zhang%2C+Tao%22">Zhang, Tao</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Li%2C+Yulin%22">Li, Yulin</searchLink><i> liyl@lzu.edu.cn</i>
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  Data: <searchLink fieldCode="DE" term="%22Stille+reaction%22">Stille reaction</searchLink><br /><searchLink fieldCode="DE" term="%22Asymmetric+synthesis%22">Asymmetric synthesis</searchLink>
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  Data: An efficient total synthesis of (±)-isocembrene via an intramolecular Stille cross-coupling reaction is described. A novel strategy towards the 1,3-diene-based cembrane-type macrocyclic diterpenoids has been realized. [Copyright &y& Elsevier]
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  Data: <i>Copyright of Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry is the property of Pergamon Press - An Imprint of Elsevier Science and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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      – Type: doi
        Value: 10.1016/S0040-4039(03)01408-4
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      – Code: eng
        Text: English
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      – SubjectFull: Asymmetric synthesis
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      – TitleFull: Studies on novel macrocyclization methods of cembrane-type diterpenoids: a Stille cyclization approach to (±)-isocembrene
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            NameFull: Peng, Lizeng
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              Text: Jul2003
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              Y: 2003
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            – TitleFull: Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry
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