Chemistry of ethanediyl S,S-acetals 9-asymmetric synthesis of chiral cis allylic alcohols

Article abstract of DOI:10.1080/00397919508011763

(2Z,1S)-1,3-diphenyl-2-propenol is obtained from the chiral 5,6-dihydro-1,4-dithiin 1b in two steps and 60% enantiomeric excess. Combining our previously reported stereoselective double bond formation and this 1,4 asymmetric induction introduces a new rou

Full text of DOI:10.1080/00397919508011763

This article was downloaded by: [Michigan State University]
On: 03 February 2015, At: 04:08
Publisher: Taylor & Francis
Informa Ltd Registered in England and Wales Registered Number: 1072954
Registered office: Mortimer House, 37-41 Mortimer Street, London W1T 3JH, UK
Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic Organic
Chemistry
Publication details, including instructions for authors and
subscription information:
http://www.tandfonline.com/loi/lsyc20
Chemistry of Ethanediyl S,S-Acetals
9-Asymmetric Synthesis of Chiral cis
Allylic Alcohols
a
a
a
Rornualdo Caputo , Carla Ferreri , Giovanni Palumbo
&
a
Silvana Pedatella
a
Dipartimento di Chimica Organica e Biologica
dell'Università , Via Mezzocannone 16, I-80134, Napoli, Italy
Published online: 23 Sep 2006.
To cite this article: Rornualdo Caputo , Carla Ferreri , Giovanni Palumbo & Silvana Pedatella
(1995) Chemistry of Ethanediyl S,S-Acetals 9-Asymmetric Synthesis of Chiral cis Allylic
Alcohols, Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 25:10, 1517-1522, DOI: 10.1080/00397919508011763
To link to this article: http://dx.doi.org/10.1080/00397919508011763
PLEASE SCROLL DOWN FOR ARTICLE
Taylor & Francis makes every effort to ensure the accuracy of all the information
(
&
the “Content”) contained in the publications on our platform. However, Taylor
Francis, our agents, and our licensors make no representations or warranties
whatsoever as to the accuracy, completeness, or suitability for any purpose of the
Content. Any opinions and views expressed in this publication are the opinions and
views of the authors, and are not the views of or endorsed by Taylor & Francis. The
accuracy of the Content should not be relied upon and should be independently
verified with primary sources of information. Taylor and Francis shall not be liable
for any losses, actions, claims, proceedings, demands, costs, expenses, damages,
and other liabilities whatsoever or howsoever caused arising directly or indirectly in
connection with, in relation to or arising out of the use of the Content.

This article may be used for research, teaching, and private study purposes. Any
substantial or systematic reproduction, redistribution, reselling, loan, sub-licensing,
systematic supply, or distribution in any form to anyone is expressly forbidden.
Terms & Conditions of access and use can be found at http://www.tandfonline.com/
page/terms-and-conditions