Literature DB >> 27043010

Synthesis of the C22-C40 Domain of the Azaspiracids.

Zhigao Zhang1, Yong Chen1, Daniel Adu-Ampratwum1, Antony Akura Okumu1, Nathaniel T Kenton1, Craig J Forsyth1.   

Abstract

An efficient synthesis of the C22-C40 domain of the azaspiracids is described. The synthetic route features a Nozaki-Hiyama-Kishi (NHK) coupling and chelation controlled Mukaiyama aldol reaction to access an acyclic intermediate and a double-intramolecular-hetero-Michael addition (DIHMA) to provide the FG-ring system bridged ketal.

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Year:  2016        PMID: 27043010     DOI: 10.1021/acs.orglett.6b00557

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


  2 in total

1.  Synthesis of the 8,19-Epoxysteroid Eurysterol A.

Authors:  Ömer Taspinar; Tobias Wilczek; Julian Erver; Martin Breugst; Jörg-Martin Neudörfl; Hans-Günther Schmalz
Journal:  Chemistry       Date:  2020-03-09       Impact factor: 5.236

2.  Synthesis and Anti-Hepatitis B Activities of 3'-Fluoro-2'-Substituted Apionucleosides.

Authors:  Martin Holan; Kathryn Tucker; Natalia Dyatkina; Hong Liu; April Kinkade; Guangyi Wang; Zhinan Jin; Marija Prhavc
Journal:  Molecules       Date:  2022-04-08       Impact factor: 4.411

  2 in total

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