Literature DB >> 19847349

Synthetic approaches to the bicyclo[2.2.2]diazaoctane ring system common to the paraherquamides, stephacidins and related prenylated indole alkaloids.

Kenneth A Miller1, Robert M Williams.   

Abstract

The bicyclo[2.2.2]diazaoctane ring system is common to a number of highly biologically active secondary metabolites isolated from numerous species of fungi. In this tutorial review, we describe the varied synthetic approaches that have been employed to construct this ring system in the course of recent total synthesis endeavors, and this review should be of interest to synthetic organic chemists and natural product chemists. Detailed herein are a number of synthetic disconnections including intramolecular S(N)2' cyclizations, biomimetic Diels-Alder reactions, radical cyclizations, and cationic cascade reactions.

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Year:  2009        PMID: 19847349      PMCID: PMC2839869          DOI: 10.1039/b816705m

Source DB:  PubMed          Journal:  Chem Soc Rev        ISSN: 0306-0012            Impact factor:   54.564


  19 in total

1.  Asymmetric total synthesis of (-)-VM55599: establishment of the absolute stereochemistry and biogenetic implications.

Authors:  Juan F Sanz-Cervera; Robert M Williams
Journal:  J Am Chem Soc       Date:  2002-03-20       Impact factor: 15.419

2.  Asymmetric, stereocontrolled total synthesis of paraherquamide A.

Authors:  Robert M Williams; Jianhua Cao; Hidekazu Tsujishima; Rhona J Cox
Journal:  J Am Chem Soc       Date:  2003-10-08       Impact factor: 15.419

3.  Total synthesis of avrainvillamide (CJ-17,665) and stephacidin B.

Authors:  Phil S Baran; Carlos A Guerrero; Benjamin D Hafensteiner; Narendra B Ambhaikar
Journal:  Angew Chem Int Ed Engl       Date:  2005-06-20       Impact factor: 15.336

4.  A concise, biomimetic total synthesis of stephacidin A and notoamide B.

Authors:  Thomas J Greshock; Alan W Grubbs; Sachiko Tsukamoto; Robert M Williams
Journal:  Angew Chem Int Ed Engl       Date:  2007       Impact factor: 15.336

5.  Concise total synthesis of (+/-)-marcfortine B.

Authors:  Barry M Trost; Nicolai Cramer; Heiko Bernsmann
Journal:  J Am Chem Soc       Date:  2007-02-22       Impact factor: 15.419

6.  Intermolecular and intramolecular Diels-Alder cycloadditions of 3-ylidenepiperazine-2,5-diones and 5-acyloxy-2(1h)-pyrazinones.

Authors:  S Jin; P Wessig; J Liebscher
Journal:  J Org Chem       Date:  2001-06-01       Impact factor: 4.354

Review 7.  Paraherquamides, brevianamides, and asperparalines: laboratory synthesis and biosynthesis. An interim report.

Authors:  Robert M Williams; Rhona J Cox
Journal:  Acc Chem Res       Date:  2003-02       Impact factor: 22.384

Review 8.  Total synthesis and biosynthesis of the paraherquamides: an intriguing story of the biological Diels-Alder construction.

Authors:  Robert Michael Williams
Journal:  Chem Pharm Bull (Tokyo)       Date:  2002-06       Impact factor: 1.645

9.  Improved biomimetic total synthesis of D,L-stephacidin A.

Authors:  Thomas J Greshock; Robert M Williams
Journal:  Org Lett       Date:  2007-09-14       Impact factor: 6.005

10.  Concise, Biomimetic Total Synthesis of d,l-Marcfortine C.

Authors:  Thomas J Greshock; Alan W Grubbs; Robert M Williams
Journal:  Tetrahedron       Date:  2007-07-02       Impact factor: 2.457

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  19 in total

Review 1.  Enantiomeric natural products: occurrence and biogenesis.

Authors:  Jennifer M Finefield; David H Sherman; Martin Kreitman; Robert M Williams
Journal:  Angew Chem Int Ed Engl       Date:  2012-05-03       Impact factor: 15.336

2.  Intermolecular Diels-Alder Cycloaddition for the Construction of Bicyclo[2.2.2]diazaoctane Structures: Formal Synthesis of Brevianamide B and Premalbrancheamide.

Authors:  Jacob G Robins; Kyu J Kim; Alex J Chinn; John S Woo; Jonathan R Scheerer
Journal:  J Org Chem       Date:  2016-02-26       Impact factor: 4.354

3.  Studies on the Biosynthesis of the Stephacidin and Notoamide Natural Products: A Stereochemical and Genetic Conundrum.

Authors:  James D Sunderhaus; David H Sherman; Robert M Williams
Journal:  Isr J Chem       Date:  2011-04       Impact factor: 3.333

Review 4.  Natural products synthesis: enabling tools to penetrate Nature's secrets of biogenesis and biomechanism.

Authors:  Robert M Williams
Journal:  J Org Chem       Date:  2011-04-12       Impact factor: 4.354

Review 5.  Fungal origins of the bicyclo[2.2.2]diazaoctane ring system of prenylated indole alkaloids.

Authors:  Jennifer M Finefield; Jens C Frisvad; David H Sherman; Robert M Williams
Journal:  J Nat Prod       Date:  2012-04-15       Impact factor: 4.050

6.  Bioconversion of 6-epi-Notoamide T Produces Metabolites of Unprecedented Structures in a Marine-derived Aspergillus sp.

Authors:  Hikaru Kato; Takashi Nakahara; Michitaka Yamaguchi; Ippei Kagiyama; Jennifer M Finefield; James D Sunderhaus; David H Sherman; Robert M Williams; Sachiko Tsukamoto
Journal:  Tetrahedron Lett       Date:  2015-01-01       Impact factor: 2.415

7.  Flavin-Dependent Monooxygenases NotI and NotI' Mediate Spiro-Oxindole Formation in Biosynthesis of the Notoamides.

Authors:  Amy E Fraley; Hong T Tran; Samantha P Kelly; Sean A Newmister; Ashootosh Tripathi; Hikaru Kato; Sachiko Tsukamoto; Lei Du; Shengying Li; Robert M Williams; David H Sherman
Journal:  Chembiochem       Date:  2020-05-14       Impact factor: 3.164

8.  Synthesis and bioconversions of notoamide T: a biosynthetic precursor to stephacidin A and notoamide B.

Authors:  James D Sunderhaus; Timothy J McAfoos; Jennifer M Finefield; Hikaru Kato; Shengying Li; Sachiko Tsukamoto; David H Sherman; Robert M Williams
Journal:  Org Lett       Date:  2012-12-18       Impact factor: 6.005

9.  Palladium-catalyzed synthesis of N-tert-prenylindoles.

Authors:  Kirsten F Johnson; Ryan Van Zeeland; Levi M Stanley
Journal:  Org Lett       Date:  2013-05-28       Impact factor: 6.005

10.  Total synthesis of aspeverin via an iodine(III)-mediated oxidative cyclization.

Authors:  Adam M Levinson
Journal:  Org Lett       Date:  2014-08-29       Impact factor: 6.005

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