Please use this identifier to cite or link to this item: https://doi.org/10.1021/ol006918c
Title: Synthetic studies toward anisatin: A formal synthesis of (±)-8-deoxyanisatin
Authors: Loh, T.-P. 
Hu, Q.-Y.
Issue Date: 25-Jan-2001
Source: Loh, T.-P., Hu, Q.-Y. (2001-01-25). Synthetic studies toward anisatin: A formal synthesis of (±)-8-deoxyanisatin. Organic Letters 3 (2) : 279-281. ScholarBank@NUS Repository. https://doi.org/10.1021/ol006918c
Abstract: equations presented An efficient strategy to construct the congested C-7a quaternary chiral center of anisatin was developed, by way of an Eschenmoser-Claisen rearrangement. Conversion of the resultant amide to Kende's ε-lactone intermediate 3 in four steps completed a concise formal synthesis of (±)-8-deoxyanisatin (2).
Source Title: Organic Letters
URI: http://scholarbank.nus.edu.sg/handle/10635/77203
ISSN: 15237060
DOI: 10.1021/ol006918c
Appears in Collections:Staff Publications

Show full item record
Files in This Item:
There are no files associated with this item.

SCOPUSTM   
Citations

32
checked on Feb 14, 2018

WEB OF SCIENCETM
Citations

26
checked on Jan 24, 2018

Page view(s)

22
checked on Feb 12, 2018

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.