Issue 14, 2014
From the journal:

Chemical Communications

Catalytic asymmetric synthesis of 1,3-enyne scaffolds: design and synthesis of conjugated nitro dienynes as novel Michael acceptors and development of a new synthetic methodology†

Xiang Li,a   Fangzhi Peng,*a   Mingtao Zhou,a   Mingjie Mo,a   Ruirui Zhaoa  and  Zhihui Shao*a  

* Corresponding authors

a Key Laboratory of Medicinal Chemistry for Natural Resource, Ministry of Education, School of Chemical Science and Technology, Yunnan University, Kunming 650091, China
E-mail: pengfangzhi@ynu.edu.cn, zhihui_shao@hotmail.com
Fax: +86-871-65035538

Abstract

A novel catalytic enantioselective synthesis of functionalized 1,3-enynes has been developed featuring the design and synthesis of conjugated nitro dienynes as a useful new class of Michael acceptors. Moreover, a simple, yet flexible catalytic cascade approach to functionalized enantioenriched acyclic α,β-enones and cyclic dienones has also been developed.

Graphical abstract: Catalytic asymmetric synthesis of 1,3-enyne scaffolds: design and synthesis of conjugated nitro dienynes as novel Michael acceptors and development of a new synthetic methodology

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C3CC48951E
Article type
Communication
Submitted
23 Nov 2013
Accepted
13 Dec 2013
First published
16 Dec 2013

Chem. Commun., 2014,50, 1745-1747

Author version available

Download author version (PDF)

Permissions

Request permissions

Catalytic asymmetric synthesis of 1,3-enyne scaffolds: design and synthesis of conjugated nitro dienynes as novel Michael acceptors and development of a new synthetic methodology

X. Li, F. Peng, M. Zhou, M. Mo, R. Zhao and Z. Shao, Chem. Commun., 2014, 50, 1745 DOI: 10.1039/C3CC48951E

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.

Social activity

Spotlight

Advertisements