A New Family of Chelating Diphosphines with a Transition Metal Stereocenter in the Backbone: Novel Applications of "Chiral-at-Rhenium" Complexes in Rhodium-Catalyzed Enantioselective Alkene Hydrogenations
The title compounds are accessed by sequences starting with racemic and enantiomerically pure [(η5‐C5H5)Re(NO)(PPh3)(CH3)]. Reactions with chlorobenzene/HBF4, PPh2H, and tBuOK give the phosphido complex [(η5‐C5H5)Re(NO)(PPh3)(PPh2)] (3). Reactions with Ph3C+BF4−, PPh2H, and tBuOK give the methylene...
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Published in | Chemistry : a European journal Vol. 7; no. 9; pp. 2015 - 2027 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
WILEY-VCH Verlag GmbH
04.05.2001
WILEY‐VCH Verlag GmbH |
Subjects | |
Online Access | Get full text |
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Summary: | The title compounds are accessed by sequences starting with racemic and enantiomerically pure [(η5‐C5H5)Re(NO)(PPh3)(CH3)]. Reactions with chlorobenzene/HBF4, PPh2H, and tBuOK give the phosphido complex [(η5‐C5H5)Re(NO)(PPh3)(PPh2)] (3). Reactions with Ph3C+BF4−, PPh2H, and tBuOK give the methylene homologue [(η5‐C5H5)Re(NO)(PPh3)(CH2PPh2)] (9). Treatment of 3 or 9 with nBuLi or tBuLi and then PPh2Cl gives the diphosphido systems [(η5‐C5H4PPh2)Re(NO)(PPh3)((CH2)nPPh2)] (n=0/1, 5/11). Reactions of 5 and 11 with [Rh(NBD)Cl]2/AgPF6 (NBD=norbornadiene) give the rhenium/rhodium chelate complexes [(η5‐C5H4PPh2)Re(NO)(PPh3)((μ‐CH2)nPPh2)Rh(NBD)]+ PF6− (n=0/1, 6+/12+ PF6−; 30–32 % overall from commercial Re2(CO)10). The crystal structures of 6+ PF6− and 12+ PF6− are compared to those of 3 and 9, and other rhodium complexes of chelating bis(diphenylphosphines). The chiral pockets defined by the PPh2 groups show unusual features. Four alkenes of the type (Z)‐RCH=C(NHCOCH3)CO2R′ are treated with H2 (1 atm) and (R)‐6+ PF6− or (S)‐12+ PF6− (0.5 mol %) in THF at room temperature. Protected amino acids are obtained in 70–98 % yields and 93–82 % ee [(R)‐6+ PF6−] or 72–60 % ee [(S)‐12+ PF6−]. Pressure and temperature effects are defined, and turnover numbers of >1600 are realized.
Easily resolved chiral rhenium complexes [(η5‐C5H4X)Re(NO)(PPh3)(X′)], see figure, are used as scaffolds for the title compounds and reactions. This chelate family may prove to be as useful in enantioselective catalysis as those based upon chiral ferrocenes. |
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Bibliography: | ArticleID:CHEM2015 ark:/67375/WNG-JLDLVBMP-K istex:A0A9991421C6C46F303B0153CCD4ED10C410E85C ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0947-6539 1521-3765 |
DOI: | 10.1002/1521-3765(20010504)7:9<2015::AID-CHEM2015>3.0.CO;2-H |