Journal of Organic Chemistry 2005-04-15

A novel formal total synthesis of cephalotaxine.

Wei-Dong Z Li, Bao-Chun Ma

Index: J. Org. Chem. 70(8) , 3277-80, (2005)

Full Text: HTML

Abstract

A formal total synthesis of cephalotaxine (CET), the parent structure of antileukemia Cephalotaxus alkaloids, was achieved through a novel synthesis of the pentacyclic amino enone 4 by a rapid annulation of readily available beta-(3,4-methylenedioxy)phenethylamine (2), delta-valerolactone, and bromoacetone.


Related Compounds

Related Articles:

Antimicrobial properties of Kalanchoe blossfeldiana: a focus on drug resistance with particular reference to quorum sensing-mediated bacterial biofilm formation.

2015-07-01

[J. Pharm. Pharmacol. 67 , 951-62, (2015)]

Characterization of the PON1 active site using modeling simulation, in relation to PON1 lactonase activity

2008-01-01

[Bioorg. Med. Chem. 16 , 7504-9, (2008)]

5- and 6-membered (thio)lactones are prodrug type carbonic anhydrase inhibitors.

2012-01-01

[Bioorg. Med. Chem. Lett. 22 , 267-70, (2012)]

High affinity, stability, and lactonase activity of serum paraoxonase PON1 anchored on HDL with ApoA-I.

2005-09-06

[Biochemistry 44(35) , 11843-54, (2005)]

Switching of polymerization activity of cinnamoyl-alpha-cyclodextrin.

2009-04-21

[Org. Biomol. Chem. 7(8) , 1646-51, (2009)]

More Articles...