How to Submit
Browse
Events
Communities
About

Enantioselective Addition of Pyrazoles to Dienes

28 April 2021, Version 1
Working Paper
This content is an early or alternative research output and has not been peer-reviewed by Cambridge University Press at the time of posting.

Abstract

We report the first enantioselective addition of pyrazoles to 1,3-dienes. Secondary and tertiary allylic pyrazoles can be generated with excellent regioselectivity. Mechanistic studies support a pathway distinct from previous hydroaminations: a Pd(0)-catalyzed ligand-to?ligand hydrogen transfer (LLHT). This hydroamination tolerates a range of functional groups and provides a breakthrough in hydrofunctionalization of dienes.

Keywords

pyrazole
1,3-diene
hydroamination
Pd catalysis
enantioselective

Supplementary materials

Title
Description
Actions
Title
Dong Pyrazole Hydroamination SI
Description
Actions

Comments

Comments are not moderated before they are posted, but they can be removed by the site moderators if they are found to be in contravention of our Commenting and Discussion Policy [opens in a new tab] - please read this policy before you post. Comments should be used for scholarly discussion of the content in question. You can find more information about how to use the commenting feature here [opens in a new tab] .
This site is protected by reCAPTCHA and the Google Privacy Policy [opens in a new tab] and Terms of Service [opens in a new tab] apply.

Now Published

Enantioselective Addition of Pyrazoles to Dienes** [opens in a new tab]
Alexander Y. Jiu, Hannah S. Slocumb, Charles S. Yeung, Xiao‐Hui Yang, Vy M. Dong journal article
Angewandte Chemie International Edition , Volume 60, Issue 36
Online publication date: Aug, 2021

Version History

Apr 28, 2021 Version 1

Metrics

2,095
699
0
Views
Downloads
Citations

License

CC logo
CC
BY logo
BY
NC logo
NC
ND logo
ND
The content is available under CC BY NC ND 4.0 [opens in a new tab]

DOI

10.26434/chemrxiv.14489379.v1
D O I: 10.26434/chemrxiv.14489379.v1 [opens in a new tab]

Author’s competing interest statement

No conflict of interest

Share