Literature DB >> 28601672

Oxidation of 3,5-di-C-(per-O-acetylglucopyranosyl)phloroacetophenone in the synthesis of hydroxysafflor yellow A.

Toshiyuki Suzuki1, Mitsuo Ishida1, Toshihiro Kumazawa1, Shingo Sato2.   

Abstract

In the synthesis of the main yellow pigment hydroxysafflor yellow A (HSYA), that is present in safflower petals, the key compound 4-(S)-2-acetyl-4,6-di-C-(per-O-acetyl-β-D-glucosyl)-3,4-dihydroxy-5-methoxycyclohexa-2,5-dienone (11b) was diastereoselectively synthesized in an overall yield of 18% from di-C-β-D-glucosylphloroacetophenone per-O-acetate (8).
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  C-glycosylquinochalcone; Diastereoselectivity; Hydroxysafflor yellow A; Intramolecular condensation; Oxidation; Safflower petal

Mesh:

Substances:

Year:  2017        PMID: 28601672     DOI: 10.1016/j.carres.2017.05.009

Source DB:  PubMed          Journal:  Carbohydr Res        ISSN: 0008-6215            Impact factor:   2.104


  1 in total

1.  The discovery of new phloroglucinol glycosides from Agrimonia pilosa and the mechanism of oxidative dearomatization of the methyl-substituted phloroglucinol derivatives.

Authors:  Jia Zhang; Ya-Nan Yang; Jian-Shuang Jiang; Zi-Ming Feng; Xiang Yuan; Xu Zhang; Pei-Cheng Zhang
Journal:  RSC Adv       Date:  2021-06-24       Impact factor: 3.361

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.