Vincamine by synthesis and semi-synthesis-Reference-Cited by-同舟云学术

Vincamine by synthesis and semi-synthesis

Published:2020-07-03 Issue:1 Volume:20 Page:343-365
ISSN:1568-7767
Container-title:Phytochemistry Reviews
language:en
Short-container-title:Phytochem Rev

Author:

Bonandi Elisa,Foschi Francesca,Marucci Cristina,Paladino Giuseppe,Luzzani Marcello,Passarella Daniele^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Plant Science,Biotechnology

Link

https://link.springer.com/content/pdf/10.1007/s11101-020-09702-8.pdf

Reference43 articles.

1. Alves JCF, Simas ABC, Costa PRR et al (1997) Stereocontrolled elaboration of quaternary carbon centers involving the asymmetric Michael-type alkylation of chiral imines: an efficient enantioselective access to (+)-vincamine. Tetrahedron Asymmetry 8:1963–1966

2. Alves JCF, Simas ABC, Costa PRR (1999) Formal enantioselective synthesis of (+)-vincamine. The first enantioselective route to (+)-3,14-epivincamine and its enantiomer. Tetrahedron Asymmetry 10:297–306

3. Archna VH, Sharma RB et al (2016) Pharmacological reputation of vinca plant—a review. World J Pharm Pharm Sci 5:1602–1610

4. Chattopadhyay RR (1999) A comparative evaluation of some blood sugar lowering agents of plant origin. J Ethnopharmacol 67:367–372

5. Chattopadhyay RR, Sarkar SK, Ganguly S et al (1991) Hypoglycemic and antihyperglycemic effect of leaves of Vincarosealinn. Indian J Physiol Pharmacol 35:145–151

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