Literature DB >> 17078726

Electrophile-induced ether transfer: a new approach to polyketide structural units.

Kai Liu1, Richard E Taylor, Rendy Kartika.   

Abstract

[Structure: see text] A strategically novel approach to the formation of syn-1,3-diol mono- and diethers through electrophilic activation of homoallylic alkoxymethyl ethers has been developed. The resulting polyketide-like synthetic fragments are generated in good yield and with excellent stereocontrol. A chairlike transition state is proposed to account for the high stereoselectivity. Varying the conditions of the reaction workup results in the efficient generation of mono- and diether containing structural units common to polyketide natural products.

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Year:  2006        PMID: 17078726      PMCID: PMC2613644          DOI: 10.1021/ol0623318

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


  13 in total

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Authors:  Richard E Taylor; Meizhong Jin
Journal:  Org Lett       Date:  2003-12-25       Impact factor: 6.005

2.  Toward the total synthesis of natural peloruside a: stereoselective synthesis of the backbone of the core.

Authors:  Bo Liu; Wei-Shan Zhou
Journal:  Org Lett       Date:  2004-01-08       Impact factor: 6.005

3.  Total synthesis and absolute configuration of the novel microtubule-stabilizing agent peloruside A.

Authors:  Xibin Liao; Yusheng Wu; Jef K De Brabander
Journal:  Angew Chem Int Ed Engl       Date:  2003-04-11       Impact factor: 15.336

4.  Stereoselective synthesis of the C(1)-C(11) fragment of peloruside A.

Authors:  Robert M Owen; William R Roush
Journal:  Org Lett       Date:  2005-09-01       Impact factor: 6.005

5.  A double iodoetherification of sigma-symmetric diene acetals for installing four stereogenic centers in a single operation: short asymmetric total synthesis of rubrenolide.

Authors:  Hiromichi Fujioka; Yusuke Ohba; Hideki Hirose; Kenichi Murai; Yasuyuki Kita
Journal:  Angew Chem Int Ed Engl       Date:  2005-01-21       Impact factor: 15.336

6.  Total synthesis of (+)-peloruside A.

Authors:  Meizhong Jin; Richard E Taylor
Journal:  Org Lett       Date:  2005-03-31       Impact factor: 6.005

Review 7.  Toward a commercial synthesis of (+)-discodermolide.

Authors:  Stuart J Mickel
Journal:  Curr Opin Drug Discov Devel       Date:  2004-11

8.  Toward the synthesis of peloruside a: fragment synthesis and coupling studies.

Authors:  Ian Paterson; M Emilia Di Francesco; Toralf Kühn
Journal:  Org Lett       Date:  2003-02-20       Impact factor: 6.005

9.  Divergent kinetic control of classical versus ozonolytic lactonization: mechanism-based diastereoselection.

Authors:  Thomas R Hoye; Troy D Ryba
Journal:  J Am Chem Soc       Date:  2005-06-15       Impact factor: 15.419

10.  Isotactic polymethoxydienes from the Philippines sponge Myriastra clavosa.

Authors:  M Rama Rao; D John Faulkner
Journal:  J Nat Prod       Date:  2002-08       Impact factor: 4.050

View more
  5 in total

1.  Toward an enantioselective synthesis of (-)-zampanolide: preparation of the C9-C20 region.

Authors:  Matthew R Wilson; Richard E Taylor
Journal:  Org Lett       Date:  2012-06-21       Impact factor: 6.005

2.  Concise enantioselective synthesis of diospongins A and B.

Authors:  Eric Stefan; Ansel P Nalin; Richard E Taylor
Journal:  Tetrahedron       Date:  2013-09-09       Impact factor: 2.457

3.  Total Synthesis and Structural Reassignment of Lyngbyaloside C Highlighted by Intermolecular Ketene Esterification.

Authors:  Chia-Fu Chang; Eric Stefan; Richard E Taylor
Journal:  Chemistry       Date:  2015-06-23       Impact factor: 5.236

4.  Stereoselective synthesis of the C9-C19 fragment of lyngbyaloside B and C via ether transfer.

Authors:  Eric Stefan; Richard E Taylor
Journal:  Org Lett       Date:  2012-06-20       Impact factor: 6.005

Review 5.  Contemporary Strategies for the Synthesis of Tetrahydropyran Derivatives: Application to Total Synthesis of Neopeltolide, a Marine Macrolide Natural Product.

Authors:  Haruhiko Fuwa
Journal:  Mar Drugs       Date:  2016-03-25       Impact factor: 5.118

  5 in total

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