Literature DB >> 15108149

An efficient synthesis of lactacystin beta-lactone.

Timothy J Donohoe1, Herman O Sintim, Leena Sisangia, John D Harling.   

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Year:  2004        PMID: 15108149     DOI: 10.1002/anie.200453843

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


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  5 in total

1.  Diastereoselective, three-component cascade synthesis of tetrahydrofurans and tetrahydropyrans employing the tandem Mukaiyama aldol-lactonization process.

Authors:  T Andrew Mitchell; Cunxiang Zhao; Daniel Romo
Journal:  J Org Chem       Date:  2008-12-19       Impact factor: 4.354

Review 2.  Neurotrophic natural products: chemistry and biology.

Authors:  Jing Xu; Michelle H Lacoske; Emmanuel A Theodorakis
Journal:  Angew Chem Int Ed Engl       Date:  2013-12-18       Impact factor: 15.336

3.  Stereospecific total syntheses of proteasome inhibitors omuralide and lactacystin.

Authors:  Wenxin Gu; Richard B Silverman
Journal:  J Org Chem       Date:  2011-09-27       Impact factor: 4.354

4.  Diastereoselective synthesis of tetrahydrofurans via mead reductive cyclization of keto-beta-lactones derived from the tandem Mukaiyama aldol lactonization (TMAL) process.

Authors:  T Andrew Mitchell; Daniel Romo
Journal:  J Org Chem       Date:  2007-11-01       Impact factor: 4.354

5.  Evolution of the Dearomative Functionalization of Activated Quinolines and Isoquinolines: Expansion of the Electrophile Scope.

Authors:  Marvin Kischkewitz; Bruno Marinic; Nicolas Kratena; Yonglin Lai; Hamish B Hepburn; Mark Dow; Kirsten E Christensen; Timothy J Donohoe
Journal:  Angew Chem Int Ed Engl       Date:  2022-05-13       Impact factor: 16.823

  5 in total

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