Literature DB >> 14723519

Synthetic approaches to guanacastepenes. Enantiospecific syntheses of BC and AB ring systems of guanacastepenes and rameswaralide.

A Srikrishna1, Dattatraya H Dethe.   

Abstract

[reaction: see text] A simple and efficient approach for the BC and AB ring systems of the novel diterpenes guanacastepenes and rameswaralide starting from the readily and abundantly available monoterpene (R)-carvone employing RCM reaction as the key step is described.

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Year:  2004        PMID: 14723519     DOI: 10.1021/ol036057i

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  4 in total

1.  Synthesis of a Tricyclic Core of Rameswaralide.

Authors:  Barry M Trost; Hien M Nguyen; Christopher Koradin
Journal:  Tetrahedron Lett       Date:  2010-12-01       Impact factor: 2.415

2.  Bridging the gap between natural product synthesis and drug discovery.

Authors:  Nathanyal J Truax; Daniel Romo
Journal:  Nat Prod Rep       Date:  2020-10-26       Impact factor: 13.423

Review 3.  Polycyclic Furanobutenolide-Derived Cembranoid and Norcembranoid Natural Products: Biosynthetic Connections and Synthetic Efforts.

Authors:  Robert A Craig; Brian M Stoltz
Journal:  Chem Rev       Date:  2017-05-18       Impact factor: 60.622

4.  Pharmacophore-Directed Retrosynthesis Applied to Rameswaralide: Synthesis and Bioactivity of Sinularia Natural Product Tricyclic Cores.

Authors:  Nathanyal J Truax; Safiat Ayinde; Khoi Van; Jun O Liu; Daniel Romo
Journal:  Org Lett       Date:  2019-09-09       Impact factor: 6.005

  4 in total

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