Issue 4, 1995
From the journal:

Journal of the Chemical Society, Chemical Communications

Enantioselective radical-mediated reduction of α-iodolactone using tributyltin hydride in the presence of a chiral amine and a Lewis acid

Masatoshi Murakata,   Hideyuki Tsutsui  and  Osamu Hoshino  

Abstract

Enantioselective radical-mediated reduction of α-methoxymethyl-α-iododihydrocoumarin 1 using tributyltin hydride is realized in up to 62% enantiomeric excess (e.e.)(88% chemical yield) by combination of chiral diamine 2 and magnesium iodide.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/C39950000481
Article type
Paper

J. Chem. Soc., Chem. Commun., 1995, 481-482

Permissions

Request permissions

Enantioselective radical-mediated reduction of α-iodolactone using tributyltin hydride in the presence of a chiral amine and a Lewis acid

M. Murakata, H. Tsutsui and O. Hoshino, J. Chem. Soc., Chem. Commun., 1995, 481 DOI: 10.1039/C39950000481

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements