Concise synthesis of calystegines B2 and B3via intramolecular Nozaki–Hiyama–Kishi reaction-Reference-Cited by-同舟云学术

Concise synthesis of calystegines B2 and B3via intramolecular Nozaki–Hiyama–Kishi reaction

Published:2016 Issue:21 Volume:14 Page:4885-4896
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Wang Hong-Yao¹²³⁴⁵,Kato Atsushi⁶⁷⁸⁹,Kinami Kyoko⁶⁷⁸⁹,Li Yi-Xian¹²³⁴⁵,Fleet George W. J.¹⁰¹¹¹²¹³¹⁴,Yu Chu-Yi¹²³⁴⁵

Affiliation:

1. Beijing National Laboratory for Molecular Science (BNLMS)

2. CAS Key Laboratory of Molecular Recognition and Function

3. Institute of Chemistry

4. Chinese Academy of Sciences

5. Beijing 100190

6. Department of Hospital Pharmacy

7. University of Toyama

8. 2630 Sugitani

9. Japan

10. Chemistry Research Laboratory

11. Department of Chemistry

12. University of Oxford

13. Oxford

14. UK

Abstract

Calystegines B₂ and B₃ were synthesized with a concise and efficient strategy, which features an intramolecular Nozaki–Hiyama–Kishi (NHK) reaction as the key step.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/OB/C6OB00697C

Reference98 articles.

1. A plasmid of Rhizobium meliloti 41 encodes catabolism of two compounds from root exudate of Calystegium sepium

2. Calystegine B4, a novel trehalase inhibitor from Scopolia japonica

3. Distribution of Calystegines in Several Solanaceae

4. Identification and quantification of calystegines, polyhydroxyl nortropane alkaloids

5. Calystegins of Physalts alkekengi var. Francheti (Solanaceae). Structure Determination and their Glycosidase Inhibitory Activities

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