Literature DB >> 19775165

Assignment of the C5' relative stereochemistry in (+)-lepadin F and (+)-lepadin G and absolute configuration of (+)-lepadin G.

Gang Li1, Richard P Hsung.   

Abstract

Concise assignments of the C5' stereochemistry in (+)-lepadin F and (+)-lepadin G and the absolute configuration of (+)-lepadin G via the first total syntheses of (+)-5'-epi-lepadin F, (+)-lepadin G, and (+)-5'-epi-lepadin G are described. This work represents an illustrative example in which a diastereomeric pair can possess sufficient spectroscopic difference for clear assignment despite differing only at a highly insulated acyclic stereocenter.

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Year:  2009        PMID: 19775165      PMCID: PMC2822462          DOI: 10.1021/ol9018997

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


  11 in total

1.  Total synthesis of lepadins B, d, e, and h; determination of the configuration of the latter three alkaloids.

Authors:  Xiaotao Pu; Dawei Ma
Journal:  Angew Chem Int Ed Engl       Date:  2004-08-13       Impact factor: 15.336

2.  [3 + 3] Cycloadditions and related strategies in alkaloid natural product synthesis.

Authors:  Joseph P A Harrity; Olivier Provoost
Journal:  Org Biomol Chem       Date:  2005-03-23       Impact factor: 3.876

3.  Total synthesis of the marine alkaloid (-)-lepadin B.

Authors:  T Ozawa; S Aoyagi; C Kibayashi
Journal:  Org Lett       Date:  2000-09-21       Impact factor: 6.005

4.  Facile entry to substituted decahydroquinoline alkaloids. Total synthesis of lepadins A-E and H.

Authors:  Xiaotao Pu; Dawei Ma
Journal:  J Org Chem       Date:  2006-08-18       Impact factor: 4.354

5.  Total synthesis of the marine alkaloids (-)-lepadins a, b, and c based on stereocontrolled intramolecular acylnitroso-Diels-Alder reaction.

Authors:  T Ozawa; S Aoyagi; C Kibayashi
Journal:  J Org Chem       Date:  2001-05-18       Impact factor: 4.354

6.  Lepadins F-H, new cis-decahydroquinoline alkaloids from the Australian ascidian Aplidium tabascum.

Authors:  Rohan A Davis; Anthony R Carroll; Ronald J Quinn
Journal:  J Nat Prod       Date:  2002-04       Impact factor: 4.050

7.  Total synthesis of (+)-lepadin F.

Authors:  Gang Li; Richard P Hsung; Brian W Slafer; Irina K Sagamanova
Journal:  Org Lett       Date:  2008-09-27       Impact factor: 6.005

8.  Total Synthesis of ent-lepadin F and G by a tandem ene-yne-ene ring closing metathesis.

Authors:  Alexander Niethe; Dirk Fischer; Siegfried Blechert
Journal:  J Org Chem       Date:  2008-03-22       Impact factor: 4.354

9.  Lepadins D-F: antiplasmodial and antitrypanosomal decahydroquinoline derivatives from the tropical marine tunicate Didemnum sp.

Authors:  Anthony D Wright; Eva Goclik; Gabriele M König; Ronald Kaminsky
Journal:  J Med Chem       Date:  2002-07-04       Impact factor: 7.446

10.  Stereoselective formal [3 + 3] cycloaddition approach to cis-1-azadecalins and synthesis of (-)-4a,8a-diepi-pumiliotoxin C. evidence for the first highly stereoselective 6pi-electron electrocyclic ring closures of 1-azatrienes.

Authors:  Heather M Sklenicka; Richard P Hsung; Michael J McLaughlin; Lin-Li Wei; Aleksey I Gerasyuto; William B Brennessel
Journal:  J Am Chem Soc       Date:  2002-09-04       Impact factor: 15.419

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  3 in total

1.  Aza-[3 + 3] Annulations: A New Unified Strategy in Alkaloid Synthesis.

Authors:  Grant S Buchanan; John B Feltenberger; Richard P Hsung
Journal:  Curr Org Synth       Date:  2010-08-01       Impact factor: 1.975

2.  Asymmetric aza-[3+3] annulation in the synthesis of indolizidines: an unexpected reversal of regiochemistry.

Authors:  Grant S Buchanan; Huifang Dai; Richard P Hsung; Aleksey I Gerasyuto; Casi M Scheinebeck
Journal:  Org Lett       Date:  2011-07-25       Impact factor: 6.005

3.  Systematic comparison of sets of (13)C NMR spectra that are potentially identical. Confirmation of the configuration of a cuticular hydrocarbon from the cane beetle Antitrogus parvulus.

Authors:  Norazah Basar; Krishnan Damodaran; Hao Liu; Gareth A Morris; Hasnah M Sirat; Eric J Thomas; Dennis P Curran
Journal:  J Org Chem       Date:  2014-07-28       Impact factor: 4.354

  3 in total

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