Synthesis and absolute configuration assignment of albucidin: a late-stage reductive deiodination by visible light photocatalysis-Reference-Cited by-同舟云学术

Synthesis and absolute configuration assignment of albucidin: a late-stage reductive deiodination by visible light photocatalysis

Published:2016 Issue:13 Volume:14 Page:3482-3485
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Zhang Hu¹²³⁴⁵,Liu Peng-Fei¹²³⁴⁵,Chen Qiong¹²³⁴⁵,Wu Qiong-You¹²³⁴⁵,Seville Anne⁶⁷⁸,Gu Yu-Cheng⁶⁷⁸,Clough John⁶⁷⁸,Zhou Shao-Lin¹²³⁴⁵,Yang Guang-Fu¹²³⁴⁵

Affiliation:

1. Key Laboratory of Pesticide & Chemical Biology

2. Ministry of Education College of Chemistry

3. Central China Normal University

4. Wuhan

5. China

6. Syngenta Jealott's Hill International Research Centre

7. Bracknell

8. UK

Abstract

The total synthesis and absolute configuration assignment of albucidin might pave the way for synthetic and medicinal chemists for further research on this type of bioactive molecule.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/OB/C6OB00371K

Reference40 articles.

1. Albucidin: a novel bleaching herbicide from Streptomyces albus subsp. chlorinus NRRL B-24108

2. Synthesis and antiviral activity of oxetanocin derivatives

3. Nucleoside analogs with antiviral activity

4. S. Niitsuma , Y.-i.Ichikawa and T.Takita, in Studies in Natural Products Chemistry, ed. R. Atta ur, Elsevier, 1992, vol. 10 Part F, pp. 585–627

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