New insights into the mechanism of molybdenum-catalyzed asymmetric alkylation
Gespeichert in:
Verfasser / Beitragende:
[S. W. Krska, D. L. Hughes, R. A. Reamer, D. J. Mathre, M. Palucki, Nobuyoshi Yasuda, Y. Sun, B. M. Trost]
Ort, Verlag, Jahr:
2004
Enthalten in:
Pure and Applied Chemistry, 76/3(2004-01-01), 625-633
Format:
Artikel (online)
Online Zugang:
| LEADER | caa a22 4500 | ||
|---|---|---|---|
| 001 | 378923072 | ||
| 003 | CHVBK | ||
| 005 | 20180305123610.0 | ||
| 007 | cr unu---uuuuu | ||
| 008 | 161128e20040101xx s 000 0 eng | ||
| 024 | 7 | 0 | |a 10.1351/pac200476030625 |2 doi |
| 035 | |a (NATIONALLICENCE)gruyter-10.1351/pac200476030625 | ||
| 245 | 0 | 0 | |a New insights into the mechanism of molybdenum-catalyzed asymmetric alkylation |h [Elektronische Daten] |c [S. W. Krska, D. L. Hughes, R. A. Reamer, D. J. Mathre, M. Palucki, Nobuyoshi Yasuda, Y. Sun, B. M. Trost] |
| 520 | 3 | |a The major features of the catalytic cycle, including structures of key intermediates, have been determined for the molybdenum-catalyzed asymmetric alkylation. The crystal structure of the π-allyl intermediate exhibits 3-point binding of an anionic ligand. Based on NMR analysis, this species adopts in solution a structure consistent with that observed in the solid state. For the allylic alkylation, the crystal structure predicts the opposite stereochemistry vs. that observed experimentally, which suggests that either the reaction proceeds via a minor isomer (Curtin-Hammett conditions) or with retention of configuration. In addition, CO transfer, promoted by Mo(CO)6, has been found to play a key role in catalyst turnover. | |
| 540 | |a © 2013 Walter de Gruyter GmbH, Berlin/Boston | ||
| 700 | 1 | |a Krska |D S. W. |u Department of Process Research, Merck and Co., Inc., Rahway, NJ 07065, USA; Department of Chemistry, Stanford University, Palo Alto, CA 94305-5080, USA |4 aut | |
| 700 | 1 | |a Hughes |D D. L. |u Department of Process Research, Merck and Co., Inc., Rahway, NJ 07065, USA; Department of Chemistry, Stanford University, Palo Alto, CA 94305-5080, USA |4 aut | |
| 700 | 1 | |a Reamer |D R. A. |u Department of Process Research, Merck and Co., Inc., Rahway, NJ 07065, USA; Department of Chemistry, Stanford University, Palo Alto, CA 94305-5080, USA |4 aut | |
| 700 | 1 | |a Mathre |D D. J. |u Department of Process Research, Merck and Co., Inc., Rahway, NJ 07065, USA; Department of Chemistry, Stanford University, Palo Alto, CA 94305-5080, USA |4 aut | |
| 700 | 1 | |a Palucki |D M. |u Department of Process Research, Merck and Co., Inc., Rahway, NJ 07065, USA; Department of Chemistry, Stanford University, Palo Alto, CA 94305-5080, USA |4 aut | |
| 700 | 1 | |a Yasuda |D Nobuyoshi |u Department of Process Research, Merck and Co., Inc., Rahway, NJ 07065, USA; Department of Chemistry, Stanford University, Palo Alto, CA 94305-5080, USA |4 aut | |
| 700 | 1 | |a Sun |D Y. |u Department of Process Research, Merck and Co., Inc., Rahway, NJ 07065, USA; Department of Chemistry, Stanford University, Palo Alto, CA 94305-5080, USA |4 aut | |
| 700 | 1 | |a Trost |D B. M. |u Department of Process Research, Merck and Co., Inc., Rahway, NJ 07065, USA; Department of Chemistry, Stanford University, Palo Alto, CA 94305-5080, USA |4 aut | |
| 773 | 0 | |t Pure and Applied Chemistry |d De Gruyter |g 76/3(2004-01-01), 625-633 |x 0033-4545 |q 76:3<625 |1 2004 |2 76 |o pac | |
| 856 | 4 | 0 | |u https://doi.org/10.1351/pac200476030625 |q text/html |z Onlinezugriff via DOI |
| 908 | |D 1 |a research article |2 jats | ||
| 950 | |B NATIONALLICENCE |P 856 |E 40 |u https://doi.org/10.1351/pac200476030625 |q text/html |z Onlinezugriff via DOI | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Krska |D S. W. |u Department of Process Research, Merck and Co., Inc., Rahway, NJ 07065, USA; Department of Chemistry, Stanford University, Palo Alto, CA 94305-5080, USA |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Hughes |D D. L. |u Department of Process Research, Merck and Co., Inc., Rahway, NJ 07065, USA; Department of Chemistry, Stanford University, Palo Alto, CA 94305-5080, USA |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Reamer |D R. A. |u Department of Process Research, Merck and Co., Inc., Rahway, NJ 07065, USA; Department of Chemistry, Stanford University, Palo Alto, CA 94305-5080, USA |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Mathre |D D. J. |u Department of Process Research, Merck and Co., Inc., Rahway, NJ 07065, USA; Department of Chemistry, Stanford University, Palo Alto, CA 94305-5080, USA |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Palucki |D M. |u Department of Process Research, Merck and Co., Inc., Rahway, NJ 07065, USA; Department of Chemistry, Stanford University, Palo Alto, CA 94305-5080, USA |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Yasuda |D Nobuyoshi |u Department of Process Research, Merck and Co., Inc., Rahway, NJ 07065, USA; Department of Chemistry, Stanford University, Palo Alto, CA 94305-5080, USA |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Sun |D Y. |u Department of Process Research, Merck and Co., Inc., Rahway, NJ 07065, USA; Department of Chemistry, Stanford University, Palo Alto, CA 94305-5080, USA |4 aut | ||
| 950 | |B NATIONALLICENCE |P 700 |E 1- |a Trost |D B. M. |u Department of Process Research, Merck and Co., Inc., Rahway, NJ 07065, USA; Department of Chemistry, Stanford University, Palo Alto, CA 94305-5080, USA |4 aut | ||
| 950 | |B NATIONALLICENCE |P 773 |E 0- |t Pure and Applied Chemistry |d De Gruyter |g 76/3(2004-01-01), 625-633 |x 0033-4545 |q 76:3<625 |1 2004 |2 76 |o pac | ||
| 900 | 7 | |b CC0 |u http://creativecommons.org/publicdomain/zero/1.0 |2 nationallicence | |
| 898 | |a BK010053 |b XK010053 |c XK010000 | ||
| 949 | |B NATIONALLICENCE |F NATIONALLICENCE |b NL-gruyter | ||