Facile access to chiral ketones through metal-free oxidative C-C bond cleavage of aldehydes by O2

Giving the metal the boot: The title reaction provides facile access to functionalized chiral ketones from chiral α,α′-disubstituted aldehydes in the presence of molecular oxygen (see scheme). The CC bond-cleavage approach offers an alternative or better method relative to the typical bond-forming s...

Full description

Saved in:

Bibliographic Details
Main Authors:	Tiwari, Bhoopendra, Zhang, Junming, Chi, Robin Yonggui
Other Authors:	School of Physical and Mathematical Sciences
Format:	Article
Language:	English
Published:	2012
Subjects:	DRNTU::Engineering::Chemical engineering::Biochemical engineering
Online Access:	https://hdl.handle.net/10356/94646 http://hdl.handle.net/10220/8117
Tags:	Add Tag No Tags, Be the first to tag this record!
Institution:	Nanyang Technological University
Language:	English

id	sg-ntu-dr.10356-94646
record_format	dspace
spelling	sg-ntu-dr.10356-946462020-03-07T12:31:30Z Facile access to chiral ketones through metal-free oxidative C-C bond cleavage of aldehydes by O2 Tiwari, Bhoopendra Zhang, Junming Chi, Robin Yonggui School of Physical and Mathematical Sciences DRNTU::Engineering::Chemical engineering::Biochemical engineering Giving the metal the boot: The title reaction provides facile access to functionalized chiral ketones from chiral α,α′-disubstituted aldehydes in the presence of molecular oxygen (see scheme). The CC bond-cleavage approach offers an alternative or better method relative to the typical bond-forming strategies used in synthesizing chiral ketones. 2012-05-22T09:02:46Z 2019-12-06T18:59:36Z 2012-05-22T09:02:46Z 2019-12-06T18:59:36Z 2012 2012 Journal Article Tiwari, B., Zhang, J. & Chi, R. Y. (2012). Facile Access to Chiral Ketones through Metal-Free Oxidative CC Bond Cleavage of Aldehydes by O2. Angewandte Chemie International Edition, 51(8), 1911-1914. https://hdl.handle.net/10356/94646 http://hdl.handle.net/10220/8117 10.1002/anie.201107473 165026 en Angewandte chemie international edition © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
institution	Nanyang Technological University
building	NTU Library
country	Singapore
collection	DR-NTU
language	English
topic	DRNTU::Engineering::Chemical engineering::Biochemical engineering
spellingShingle	DRNTU::Engineering::Chemical engineering::Biochemical engineering Tiwari, Bhoopendra Zhang, Junming Chi, Robin Yonggui Facile access to chiral ketones through metal-free oxidative C-C bond cleavage of aldehydes by O2
description	Giving the metal the boot: The title reaction provides facile access to functionalized chiral ketones from chiral α,α′-disubstituted aldehydes in the presence of molecular oxygen (see scheme). The CC bond-cleavage approach offers an alternative or better method relative to the typical bond-forming strategies used in synthesizing chiral ketones.
author2	School of Physical and Mathematical Sciences
author_facet	School of Physical and Mathematical Sciences Tiwari, Bhoopendra Zhang, Junming Chi, Robin Yonggui
format	Article
author	Tiwari, Bhoopendra Zhang, Junming Chi, Robin Yonggui
author_sort	Tiwari, Bhoopendra
title	Facile access to chiral ketones through metal-free oxidative C-C bond cleavage of aldehydes by O2
title_short	Facile access to chiral ketones through metal-free oxidative C-C bond cleavage of aldehydes by O2
title_full	Facile access to chiral ketones through metal-free oxidative C-C bond cleavage of aldehydes by O2
title_fullStr	Facile access to chiral ketones through metal-free oxidative C-C bond cleavage of aldehydes by O2
title_full_unstemmed	Facile access to chiral ketones through metal-free oxidative C-C bond cleavage of aldehydes by O2
title_sort	facile access to chiral ketones through metal-free oxidative c-c bond cleavage of aldehydes by o2
publishDate	2012
url	https://hdl.handle.net/10356/94646 http://hdl.handle.net/10220/8117
_version_	1681049420313919488

Facile access to chiral ketones through metal-free oxidative C-C bond cleavage of aldehydes by O2

Similar Items