Research output: Contribution to journal › Article › peer-review
Scott David Phillips, Kristian H. O. Andersson, Nina Kann, Michael T. Kuntz, Marcia B. France, Piotr Wawrzyniak, Matt Clarke
Methods to produce a range of new phosphine-diamine ligands from phosphino-aldehydes have been developed and a hypothesis that larger P-substituents would increase the enantioselectivity towards the (S) isomer in Ru-catalysed ketone hydrogenation of acetophenone has been examined; the successful validation of this hypothesis is further evidence that the mechanism of these catalysts involves a secondary amine assisted reduction.
Original language | English |
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Pages (from-to) | 1336-1339 |
Number of pages | 4 |
Journal | Catalysis Science & Technology |
Volume | 1 |
Issue number | 8 |
DOIs | |
Publication status | Published - Nov 2011 |
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Research output: Contribution to journal › Article › peer-review
Research output: Contribution to journal › Article › peer-review
Research output: Contribution to journal › Article › peer-review
Research output: Contribution to journal › Article › peer-review
Research output: Contribution to journal › Article › peer-review
Research output: Contribution to journal › Article › peer-review
Research output: Contribution to journal › Article › peer-review
Research output: Contribution to journal › Article › peer-review
Research output: Contribution to journal › Article › peer-review
Research output: Contribution to journal › Article › peer-review
ID: 17581814