Literature DB >> 20151022

A Stereodivergent Approach for Accessing Both C2,8a-Syn and C2,8a-Anti Relative Stereochemical Manifolds in the Lepadin Family via a TiCL(4)-Promoted Aza-[3 + 3] Annulation.

Gang Li1, Lauren J Carlson, Irina K Sagamanova, Brian W Slafer, Richard P Hsung, Claudio Gilardi, Heather M Sklenicka, Nadiya Sydroenko.   

Abstract

Details in developing a stereodivergent approach to the lepadin family and establishing an entry to both C2,8a-syn and C2,8a-anti relative stereochemical manifolds through a common intermediate are described here. This works paves a foundation for constructing all members of the lepadin family, which consists of three subsets based on an array of interesting relative configurations. These efforts underline the prominence of aza-[3 + 3] annulation as a unified strategy in alkaloid synthesis.

Entities:  

Year:  2009        PMID: 20151022      PMCID: PMC2819155          DOI: 10.1055/s-0029-1216920

Source DB:  PubMed          Journal:  Synthesis (Stuttg)        ISSN: 0039-7881            Impact factor:   3.157


  40 in total

1.  A [3 + 3] annelation approach to tetrahydropyridines.

Authors:  Lisa C Pattenden; Robert A J Wybrow; Stephen A Smith; Joseph P A Harrity
Journal:  Org Lett       Date:  2006-07-06       Impact factor: 6.005

2.  Ring expansion of functionalized octahydroindoles to enantiopure cis-decahydroquinolines.

Authors:  Marisa Mena; Josep Bonjoch; Domingo Gomez Pardo; Janine Cossy
Journal:  J Org Chem       Date:  2006-08-04       Impact factor: 4.354

3.  Highly stereoselective formal

Authors: 
Journal:  Org Lett       Date:  2000-04-20       Impact factor: 6.005

4.  A novel and highly stereoselective approach to aza-spirocycles. A short total synthesis of 2-epi-(+/-)-perhydrohistrionicotoxin and an unprecedented decarboxylation of 2-pyrones.

Authors:  Michael J McLaughlin; Richard P Hsung; Kevin P Cole; Juliet M Hahn; Jiashi Wang
Journal:  Org Lett       Date:  2002-06-13       Impact factor: 6.005

5.  Total syntheses of enantiomerically enriched R-(+)- and S-(-)-deplancheine.

Authors:  Nadiya Sydorenko; Craig A Zificsak; Aleksey I Gerasyuto; Richard P Hsung
Journal:  Org Biomol Chem       Date:  2005-04-25       Impact factor: 3.876

6.  Total synthesis of (+/-)-stenine using the IMDAF cycloaddition of a 2-methylthio-5-amido-substituted furan.

Authors:  John D Ginn; Albert Padwa
Journal:  Org Lett       Date:  2002-05-02       Impact factor: 6.005

7.  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

8.  A General Approach to the Quinolizidine Alkaloids via an Intramolecular Aza-[3 + 3] Annulation. Synthesis of (±)-2-Deoxy-Lasubine II.

Authors:  Yu Zhang; Aleksey I Gerasyuto; Quincy A Long; Richard P Hsung
Journal:  Synlett       Date:  2008-01-01       Impact factor: 2.454

9.  A concise total synthesis of (-)-cylindricine C through a stereoselective intramolecular aza-[3 + 3] annulation strategy.

Authors:  Jacob J Swidorski; Jiashi Wang; Richard P Hsung
Journal:  Org Lett       Date:  2006-02-16       Impact factor: 6.005

10.  Intramolecular formal aza-[3 + 3] cycloaddition approach to indoloquinolizidine alkaloids. A stereoselective total synthesis of (+/-)-tangutorine.

Authors:  Shengjun Luo; Craig A Zificsak; Richard P Hsung
Journal:  Org Lett       Date:  2003-11-27       Impact factor: 6.005

View more
  2 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

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.