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  Why are BINOL-based monophosphites such efficient ligands in Rh-catalyzed asymmetric olefin hydrogenation?

Reetz, M. T., Meiswinkel, A., Mehler, G., Angermund, K., Graf, M., Thiel, W., et al. (2005). Why are BINOL-based monophosphites such efficient ligands in Rh-catalyzed asymmetric olefin hydrogenation? Journal of the American Chemical Society, 127(29), 10305-10313. doi:10.1021/ja052025+.

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 Creators:
Reetz, M. T.1, Author              
Meiswinkel, A.1, Author              
Mehler, G.1, Author              
Angermund, K.2, Author              
Graf, M.2, Author              
Thiel, W.2, Author              
Mynott, R.3, Author              
Blackmond, D. G.4, Author              
Affiliations:
1Research Department Reetz, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445588              
2Research Department Thiel, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445590              
3Service Department Mynott (NMR), Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445627              
4Research Group Blackmond, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445597              

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Language(s): eng - English
 Dates: 2005
 Publication Status: Published in print
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 265956
DOI: 10.1021/ja052025+
ISI: 000230700700047
 Degree: -

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Title: Journal of the American Chemical Society
  Alternative Title : J. Am. Chem. Soc.
Source Genre: Journal
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Affiliations:
Publ. Info: -
Pages: - Volume / Issue: 127 (29) Sequence Number: - Start / End Page: 10305 - 10313 Identifier: ISSN: 0002-7863