Literature DB >> 19572302

Epoxide-opening cascades in the synthesis of polycyclic polyether natural products.

Ivan Vilotijevic1, Timothy F Jamison.   

Abstract

The structural features of polycyclic polyether natural products can, in some cases, be traced to their biosynthetic origin. However in case that are less well understood, only biosynthetic pathways that feature dramatic, yet speculative, epoxide-opening cascades are proposed. We summarize how such epoxide-opening cascade reactions have been used in the synthesis of polycyclic polyethers (see scheme) and related natural products.The group of polycyclic polyether natural products is of special interest owing to the fascinating structure and biological effects displayed by its members. The latter includes potentially therapeutic antibiotic, antifungal, and anticancer properties, and extreme lethality. The polycyclic structural features of this class of compounds can, in some cases, be traced to their biosynthetic origin, but in others that are less well understood, only to proposed biosynthetic pathways that feature dramatic, yet speculative, epoxide-opening cascades. In this review we summarize how such epoxide-opening cascade reactions have been used in the synthesis of polycyclic polyethers and related natural products.

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Year:  2009        PMID: 19572302      PMCID: PMC2810545          DOI: 10.1002/anie.200900600

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  118 in total

1.  Reagent-controlled switching of 5-exo to 6-endo cyclizations in epoxide openings.

Authors:  Yoshiki Morimoto; Yoshihiro Nishikawa; Chigusa Ueba; Takeshi Tanaka
Journal:  Angew Chem Int Ed Engl       Date:  2006-01-23       Impact factor: 15.336

2.  Pertussis toxin (IAP) enhances maitotoxin (a putative Ca2+ channel agonist)-induced Ca2+ entry into synaptosomes.

Authors:  H Ueda; S Tamura; N Fukushima; H Takagi
Journal:  Eur J Pharmacol       Date:  1986-04-02       Impact factor: 4.432

3.  Total synthesis of (-)-gambierol.

Authors:  Haruhiko Fuwa; Noriko Kainuma; Kazuo Tachibana; Makoto Sasaki
Journal:  J Am Chem Soc       Date:  2002-12-18       Impact factor: 15.419

4.  Identification of NanE as the thioesterase for polyether chain release in nanchangmycin biosynthesis.

Authors:  Tiangang Liu; Delin You; Chiara Valenzano; Yuhui Sun; Jialiang Li; Qing Yu; Xiufen Zhou; David E Cane; Zixin Deng
Journal:  Chem Biol       Date:  2006-09

5.  Endo-oxacyclizations of polyepoxides: biomimetic synthesis of fused polycyclic ethers.

Authors:  Frank E McDonald; Fernando Bravo; Xia Wang; Xudong Wei; Motoki Toganoh; J Ramón Rodríguez; Bao Do; Wade A Neiwert; Kenneth I Hardcastle
Journal:  J Org Chem       Date:  2002-04-19       Impact factor: 4.354

6.  The use of 13C-NMR. Spectroscopy in biosynthetic studies. II[1]. Biosynthesis of narasin, a new polyether ionophore from fermentation of Streptomyces aureofaciens [2].

Authors:  D E Dorman; J W Paschal; W M Nakatsukasa; L L Huckstep; N Neuss
Journal:  Helv Chim Acta       Date:  1976-12-15       Impact factor: 2.164

7.  Hot water-promoted ring-opening of epoxides and aziridines by water and other nucleopliles.

Authors:  Zhi Wang; Yong-Tao Cui; Zhao-Bing Xu; Jin Qu
Journal:  J Org Chem       Date:  2008-02-21       Impact factor: 4.354

8.  Organocatalytic asymmetric epoxidation of olefins by chiral ketones.

Authors:  Yian Shi
Journal:  Acc Chem Res       Date:  2004-08       Impact factor: 22.384

9.  Biosynthesis of lasalocid. I. Incorporation of 13C and 14C labelled substrates into lasalocid A.

Authors:  J W Westley; R H Evans; G Harvey; R G Pitcher; D L Pruess
Journal:  J Antibiot (Tokyo)       Date:  1974-04       Impact factor: 2.649

10.  Polyketide synthase genes from marine dinoflagellates.

Authors:  R V Snyder; P D L Gibbs; A Palacios; L Abiy; R Dickey; J V Lopez; K S Rein
Journal:  Mar Biotechnol (NY)       Date:  2003 Jan-Feb       Impact factor: 3.619

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  29 in total

1.  Lessons and revelations from biomimetic syntheses.

Authors:  Mina Razzak; Jef K De Brabander
Journal:  Nat Chem Biol       Date:  2011-11-15       Impact factor: 15.040

2.  Formal [4+3] epoxide cascade reaction via a complementary ambiphilic pairing strategy.

Authors:  Alan Rolfe; Thiwanka B Samarakoon; Paul R Hanson
Journal:  Org Lett       Date:  2010-03-19       Impact factor: 6.005

Review 3.  Total (bio)synthesis: strategies of nature and of chemists.

Authors:  Alexandra A Roberts; Katherine S Ryan; Bradley S Moore; Tobias A M Gulder
Journal:  Top Curr Chem       Date:  2010

4.  Hydroxyl-substituted ladder polyethers via selective tandem epoxidation/cyclization sequence.

Authors:  Lara C Czabaniuk; Timothy F Jamison
Journal:  Org Lett       Date:  2015-02-03       Impact factor: 6.005

Review 5.  The development of endo-selective epoxide-opening cascades in water.

Authors:  Christopher J Morten; Jeffery A Byers; Aaron R Van Dyke; Ivan Vilotijevic; Timothy F Jamison
Journal:  Chem Soc Rev       Date:  2009-09-16       Impact factor: 54.564

6.  A metal-free aromative cascade for the synthesis of diverse heterocycles.

Authors:  Steven C Schlitzer; Dhanarajan Arunprasath; Katelyn G Stevens; Indrajeet Sharma
Journal:  Org Chem Front       Date:  2020-01-02       Impact factor: 5.281

7.  Zirconium(IV)- and hafnium(IV)-catalyzed highly enantioselective epoxidation of homoallylic and bishomoallylic alcohols.

Authors:  Zhi Li; Hisashi Yamamoto
Journal:  J Am Chem Soc       Date:  2010-06-16       Impact factor: 15.419

8.  Are molecular alphabets universal enabling factors for the evolution of complex life?

Authors:  Ian S Dunn
Journal:  Orig Life Evol Biosph       Date:  2014-02-09       Impact factor: 1.950

Review 9.  Ring opening of epoxides with C-nucleophiles.

Authors:  Sadia Faiz; Ameer Fawad Zahoor
Journal:  Mol Divers       Date:  2016-07-04       Impact factor: 2.943

Review 10.  Synthesis of marine polycyclic polyethers via endo-selective epoxide-opening cascades.

Authors:  Ivan Vilotijevic; Timothy F Jamison
Journal:  Mar Drugs       Date:  2010-03-19       Impact factor: 5.118

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