Literature DB >> 12404392

The Total Synthesis of Heliquinomycinone This work was supported by the National Institutes of Health (Grant numbers: AI 16943 and HL25848). The authors thank Dr. Makoto Chino of Nippon Kayaku Co., Ltd. for kindly providing a sample of heliquinomycin, and Yashuiro Itagaki of Columbia University for high-resolution mass spectral analyses.

Tony Siu1, Donghui Qin, Samuel J. Danishefsky.   

Abstract

Entities:  

Year:  2001        PMID： 12404392     DOI： 10.1002/1521-3773(20011217)40:24<4713::aid-anie4713>3.0.co;2-n

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


× No keyword cloud information.
  4 in total

1.  Stereoselective synthesis of benzannulated spiroketals: influence of the aromatic ring on reactivity and conformation.

Authors:  Guodong Liu; Jacqueline M Wurst; Derek S Tan
Journal:  Org Lett       Date:  2009-08-20       Impact factor: 6.005

2.  Facile synthesis of naphthoquinone spiroketals by diastereoselective oxidative [3 + 2] cycloaddition.

Authors:  Kun-Liang Wu; Stephanie Wilkinson; Norbert O Reich; Thomas R R Pettus
Journal:  Org Lett       Date:  2007-11-29       Impact factor: 6.005

3.  Enzymatic spiroketal formation via oxidative rearrangement of pentangular polyketides.

Authors:  Britta Frensch; Thorsten Lechtenberg; Michel Kather; Zeynep Yunt; Martin Betschart; Bernd Kammerer; Steffen Lüdeke; Michael Müller; Jörn Piel; Robin Teufel
Journal:  Nat Commun       Date:  2021-03-04       Impact factor: 14.919

4.  Solvent-dependent divergent functions of Sc(OTf)₃ in stereoselective epoxide-opening spiroketalizations.

Authors:  Indrajeet Sharma; Jacqueline M Wurst; Derek S Tan
Journal:  Org Lett       Date:  2014-04-17       Impact factor: 6.005
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.