Literature DB >> 14995167

Total synthesis of (+)-SCH 351448.

Eun Joo Kang1, Eun Jin Cho, Young Eun Lee, Mi Kyung Ji, Dong Mok Shin, Young Keun Chung, Eun Lee.   

Abstract

Total synthesis of SCH 351448 was accomplished employing the ring-closing olefin metathesis reaction for the preparation of the 28-membered macrodiolide.

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Year:  2004        PMID： 14995167     DOI： 10.1021/ja0315309

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN： 0002-7863            Impact factor:   15.419


  5 in total

1.  Total synthesis of (+)-SCH 351448.

Authors:  Kaicheng Zhu; James S Panek
Journal:  Org Lett       Date:  2011-08-11       Impact factor: 6.005

2.  Assignment of absolute configuration to SCH 351448 via total synthesis.

Authors:  Lael L Cheung; Shinji Marumoto; Christopher D Anderson; Scott D Rychnovsky
Journal:  Org Lett       Date:  2008-06-11       Impact factor: 6.005

3.  Efficient asymmetric synthesis of (+)-SCH 351448.

Authors:  Sergei Bolshakov; James L Leighton
Journal:  Org Lett       Date:  2005-08-18       Impact factor: 6.005

Review 4.  The genus Micromonospora as a model microorganism for bioactive natural product discovery.

Authors:  Mohamed S Hifnawy; Mohamed M Fouda; Ahmed M Sayed; Rabab Mohammed; Hossam M Hassan; Sameh F AbouZid; Mostafa E Rateb; Alexander Keller; Martina Adamek; Nadine Ziemert; Usama Ramadan Abdelmohsen
Journal:  RSC Adv       Date:  2020-06-08       Impact factor: 4.036

5.  Total Synthesis of (+)-SCH 351448: Efficiency via Chemoselectivity and Redox-Economy Powered by Metal Catalysis.

Authors:  Gang Wang; Michael J Krische
Journal:  J Am Chem Soc       Date:  2016-06-23       Impact factor: 15.419
  5 in total

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