Weak arene C - H⋅⋅⋅O hydrogen bonding in palladium-catalyzed arylation and vinylation of lactones

Weak force in action: In the title reaction, the palladium catalyst (see figure, left) uses weak CH⋅⋅⋅O hydrogen bonding to control the absolute configuration of the new stereocenter. A similar palladium catalyst (right) used conventional NH⋅⋅⋅O hydrogen bonding to guide stereoselection.

Saved in:
Bibliographic Details
Main Authors: Huang, Zhiyan, Chen, Zuliang, Lim, Li Hui, Quang, Gia Chuong Phan, Hirao, Hajime, Zhou, Jianrong Steve
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2013
Online Access:https://hdl.handle.net/10356/105487
http://hdl.handle.net/10220/16585
http://dx.doi.org/10.1002/anie.201300481
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Nanyang Technological University
Language: English
id sg-ntu-dr.10356-105487
record_format dspace
spelling sg-ntu-dr.10356-1054872019-12-06T21:52:15Z Weak arene C - H⋅⋅⋅O hydrogen bonding in palladium-catalyzed arylation and vinylation of lactones Huang, Zhiyan Chen, Zuliang Lim, Li Hui Quang, Gia Chuong Phan Hirao, Hajime Zhou, Jianrong Steve School of Physical and Mathematical Sciences Weak force in action: In the title reaction, the palladium catalyst (see figure, left) uses weak CH⋅⋅⋅O hydrogen bonding to control the absolute configuration of the new stereocenter. A similar palladium catalyst (right) used conventional NH⋅⋅⋅O hydrogen bonding to guide stereoselection. 2013-10-18T02:58:15Z 2019-12-06T21:52:15Z 2013-10-18T02:58:15Z 2019-12-06T21:52:15Z 2013 2013 Journal Article Huang, Z., Chen, Z., Lim, L. H., Quang, G. C. P., Hirao, H., & Zhou, J. S. (2013). Weak arene C - H⋅⋅⋅O hydrogen bonding in palladium-catalyzed arylation and vinylation of lactones. Angewandte chemie international edition, 52(22), 5807-5812. 1433-7851 https://hdl.handle.net/10356/105487 http://hdl.handle.net/10220/16585 http://dx.doi.org/10.1002/anie.201300481 en Angewandte chemie international edition
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
description Weak force in action: In the title reaction, the palladium catalyst (see figure, left) uses weak CH⋅⋅⋅O hydrogen bonding to control the absolute configuration of the new stereocenter. A similar palladium catalyst (right) used conventional NH⋅⋅⋅O hydrogen bonding to guide stereoselection.
author2 School of Physical and Mathematical Sciences
author_facet School of Physical and Mathematical Sciences
Huang, Zhiyan
Chen, Zuliang
Lim, Li Hui
Quang, Gia Chuong Phan
Hirao, Hajime
Zhou, Jianrong Steve
format Article
author Huang, Zhiyan
Chen, Zuliang
Lim, Li Hui
Quang, Gia Chuong Phan
Hirao, Hajime
Zhou, Jianrong Steve
spellingShingle Huang, Zhiyan
Chen, Zuliang
Lim, Li Hui
Quang, Gia Chuong Phan
Hirao, Hajime
Zhou, Jianrong Steve
Weak arene C - H⋅⋅⋅O hydrogen bonding in palladium-catalyzed arylation and vinylation of lactones
author_sort Huang, Zhiyan
title Weak arene C - H⋅⋅⋅O hydrogen bonding in palladium-catalyzed arylation and vinylation of lactones
title_short Weak arene C - H⋅⋅⋅O hydrogen bonding in palladium-catalyzed arylation and vinylation of lactones
title_full Weak arene C - H⋅⋅⋅O hydrogen bonding in palladium-catalyzed arylation and vinylation of lactones
title_fullStr Weak arene C - H⋅⋅⋅O hydrogen bonding in palladium-catalyzed arylation and vinylation of lactones
title_full_unstemmed Weak arene C - H⋅⋅⋅O hydrogen bonding in palladium-catalyzed arylation and vinylation of lactones
title_sort weak arene c - h⋅⋅⋅o hydrogen bonding in palladium-catalyzed arylation and vinylation of lactones
publishDate 2013
url https://hdl.handle.net/10356/105487
http://hdl.handle.net/10220/16585
http://dx.doi.org/10.1002/anie.201300481
_version_ 1681035926409576448