Literature DB >> 20936859

Total synthesis of the proposed structure of briarellin J.

Michael T Crimmins1, Mark C Mans, Abimael D Rodríguez.   

Abstract

The total synthesis of the originally proposed structure of briarellin J is reported in 15 steps from a known compound and in 23 steps from readily available materials. Key reactions include an exo-selective intramolecular Diels-Alder and a substrate-controlled hydroboration. Discrepancies in the spectroscopic data of the synthetic and natural material led to a revision of the assigned structure.

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Year:  2010        PMID: 20936859      PMCID: PMC2966518          DOI: 10.1021/ol102169w

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


  15 in total

1.  Asymmetric total synthesis of (-)-isolaurallene.

Authors:  M T Crimmins; K A Emmitte
Journal:  J Am Chem Soc       Date:  2001-02-21       Impact factor: 15.419

2.  An intramolecular Diels-Alder approach to the eunicellins: enantioselective total syntheses of ophirin B and astrogorgin.

Authors:  Michael T Crimmins; Brandon H Brown; Hilary R Plake
Journal:  J Am Chem Soc       Date:  2006-02-01       Impact factor: 15.419

Review 3.  Strategies for the total synthesis of C2-C11 cyclized cembranoids.

Authors:  J Michael Ellis; Michael T Crimmins
Journal:  Chem Rev       Date:  2008-12       Impact factor: 60.622

4.  Briarellins J-P and polyanthellin A: new eunicellin-based diterpenes from the gorgonian coral Briareum polyanthes and their antimalarial activity.

Authors:  Claudia A Ospina; Abimael D Rodríguez; Eduardo Ortega-Barria; Todd L Capson
Journal:  J Nat Prod       Date:  2003-03       Impact factor: 4.050

5.  New fish feeding deterrents, including a novel sesquiterpenoid heterogorgiolide, from the brazilian gorgonian heterogorgia uatumani(Octocorallia, gorgonacea)

Authors: 
Journal:  J Nat Prod       Date:  1999-09       Impact factor: 4.050

6.  An intramolecular Diels-Alder approach to the eunicelins: enantioselective total synthesis of ophirin B.

Authors:  Michael T Crimmins; Brandon H Brown
Journal:  J Am Chem Soc       Date:  2004-08-25       Impact factor: 15.419

7.  Enantioselective total synthesis of (+)-rogioloxepane A.

Authors:  Michael T Crimmins; Amy C DeBaillie
Journal:  Org Lett       Date:  2003-08-21       Impact factor: 6.005

8.  A unified strategy for enantioselective total synthesis of cladiellin and briarellin diterpenes: total synthesis of briarellins E and F and the putative structure of alcyonin and revision of its structure assignment.

Authors:  Olivier Corminboeuf; Larry E Overman; Lewis D Pennington
Journal:  J Org Chem       Date:  2009-08-07       Impact factor: 4.354

9.  An intramolecular Diels-Alder strategy for the asbestinins: enantioselective total syntheses of 11-acetoxy-4-deoxyasbestinin D and asbestinin-12.

Authors:  Michael T Crimmins; J Michael Ellis
Journal:  J Org Chem       Date:  2007-10-05       Impact factor: 4.354

10.  Studies on the minor constituents of the Caribbean gorgonian octocoral Briareum asbestinum Pallas. Isolation and structure determination of the eunicellin-based diterpenoids briarellins E--I.

Authors:  A D Rodríguez; O M Cóbar
Journal:  Chem Pharm Bull (Tokyo)       Date:  1995-11       Impact factor: 1.645

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  5 in total

Review 1.  Survey of marine natural product structure revisions: a synergy of spectroscopy and chemical synthesis.

Authors:  Takashi L Suyama; William H Gerwick; Kerry L McPhail
Journal:  Bioorg Med Chem       Date:  2011-06-12       Impact factor: 3.641

2.  Total syntheses of (+)-vigulariol and (-)-sclerophytin A.

Authors:  Michael T Crimmins; Christina S Stauffer; Mark C Mans
Journal:  Org Lett       Date:  2011-08-19       Impact factor: 6.005

3.  Origin of High Diastereoselectivity in Reactions of Seven-Membered-Ring Enolates.

Authors:  Olga Lavinda; Collin H Witt; K A Woerpel
Journal:  Angew Chem Int Ed Engl       Date:  2022-02-15       Impact factor: 15.336

4.  Synthesis and Evaluation of a 2,11-Cembranoid-Inspired Library.

Authors:  Amanda J Welford; John J Caldwell; Manjuan Liu; Meirion Richards; Nathan Brown; Cara Lomas; Graham J Tizzard; Mateusz B Pitak; Simon J Coles; Suzanne A Eccles; Florence I Raynaud; Ian Collins
Journal:  Chemistry       Date:  2016-03-01       Impact factor: 5.236

5.  Stereoselective synthesis of quaternary carbons via the dianionic Ireland-Claisen rearrangement.

Authors:  Michael T Crimmins; John D Knight; Philip S Williams; Yan Zhang
Journal:  Org Lett       Date:  2014-04-15       Impact factor: 6.005

  5 in total

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