Literature DB >> 22804345

Chirality in diarylether heptanoids: synthesis of myricatomentogenin, jugcathanin, and congeners.

M Quamar Salih1, Christopher M Beaudry.   

Abstract

The syntheses of myricatomentogenin, jugcathanin, galeon, pterocarine, and acerogenin L are reported. Synthetic material was used to measure their optical activities and free energy of activation for racemization. The natural enantiomers of myricatomentogenin, jugcathanin, galeon, and pterocarine were determined to have the same pR absolute stereochemistry. Acerogenins L and C are achiral compounds.

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Year:  2012        PMID: 22804345     DOI: 10.1021/ol301893t

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


  3 in total

1.  RECENT SYNTHETIC DEVELOPMENTS AND APPLICATIONS OF THE ULLMANN REACTION. A REVIEW.

Authors:  Hao Lin; Dianqing Sun
Journal:  Org Prep Proced Int       Date:  2013       Impact factor: 1.628

2.  Diarylheptanoid analogues from the rhizomes of Zingiber officinale and their anti-tumour activity.

Authors:  Ting Li; Da-Bo Pan; Qian-Qian Pang; Mi Zhou; Xiao-Jun Yao; Xin-Sheng Yao; Hai-Bo Li; Yang Yu
Journal:  RSC Adv       Date:  2021-09-02       Impact factor: 4.036

3.  Galeon: A Biologically Active Molecule with In Silico Metabolite Prediction, In Vitro Metabolic Profiling in Rat Liver Microsomes, and In Silico Binding Mechanisms with CYP450 Isoforms.

Authors:  A F M Motiur Rahman; Wencui Yin; Adnan A Kadi; Yurngdong Jahng
Journal:  Molecules       Date:  2020-12-13       Impact factor: 4.411

  3 in total

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