Next Article in Journal
Next Article in Special Issue
Previous Article in Journal
Previous Article in Special Issue
Molecules 2008, 13(8), 1942-2038; doi:10.3390/molecules13081942
Review

Asymmetric Synthesis of Naturally Occuring Spiroketals

 and *
Received: 21 July 2008; in revised form: 22 August 2008 / Accepted: 22 August 2008 / Published: 28 August 2008
(This article belongs to the Special Issue Spiro Compounds)
Download PDF [845 KB, uploaded 18 June 2014]
Abstract: Spiroketals are widely found as substructures of many naturally occurring compounds from diverse sources including plants, animals as well as microbes. Naturally occurring spiroketals are biologically active and most of them are chiral molecules. This article aims at reviewing the asymmetric synthesis of biologically active spiroketals for last 10 years (1998-2007).
Keywords: Synthesis; Asymmetric; Natural product; Spiroketal Synthesis; Asymmetric; Natural product; Spiroketal
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Export to BibTeX |
EndNote


MDPI and ACS Style

Raju, B.R.; Saikia, A.K. Asymmetric Synthesis of Naturally Occuring Spiroketals. Molecules 2008, 13, 1942-2038.

AMA Style

Raju BR, Saikia AK. Asymmetric Synthesis of Naturally Occuring Spiroketals. Molecules. 2008; 13(8):1942-2038.

Chicago/Turabian Style

Raju, B. R.; Saikia, Anil K. 2008. "Asymmetric Synthesis of Naturally Occuring Spiroketals." Molecules 13, no. 8: 1942-2038.


Molecules EISSN 1420-3049 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert