2006
DOI: 10.1002/chin.200604171
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Diastereoselective Addition of Mono‐ and Bis‐silylphosphines to Chiral Aldehydes.

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“…The solid was re-dissolved in hexane and X-ray quality crystals of Cr(HP{TMS} 2 )(CO) 5 (7), were grown from slow evaporation of the solvent in an inert atmosphere glove box. Pure samples of Mo(HP{TMS} 2 )(CO) 5 (8) and W(HP {TMS} 2 )(CO) 5 (9) were also obtained; however, X-ray quality crystals were not formed. 31 Table 1 contains crystal data, collection parameters and refinement criteria for compounds 4-7.…”
Section: Materials and Methodologymentioning
confidence: 99%
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“…The solid was re-dissolved in hexane and X-ray quality crystals of Cr(HP{TMS} 2 )(CO) 5 (7), were grown from slow evaporation of the solvent in an inert atmosphere glove box. Pure samples of Mo(HP{TMS} 2 )(CO) 5 (8) and W(HP {TMS} 2 )(CO) 5 (9) were also obtained; however, X-ray quality crystals were not formed. 31 Table 1 contains crystal data, collection parameters and refinement criteria for compounds 4-7.…”
Section: Materials and Methodologymentioning
confidence: 99%
“…pentane leaving a pale yellow/brown solid behind. The solid was re-dissolved in hexane and X-ray quality crystals of Cr(PhP{TMS} 2 )(CO) 5 (4), Mo(PhP{TMS} 2 ) (CO) 5 (5) and W(PhP{TMS} 2 ) (CO) 5 (6) were grown from slow evaporation of the solvent in an inert atmosphere glove box. (7), Mo (8), W (9) A solution of M(CO) 5 THF, M ¼ Cr, Mo and W was prepared by irradiating 1.1 mmol of the respective hexacarbonyl in 50 mL of THF using a high-pressure mercury lamp in 1-h increments with degassing for 3-4 h. The HP(TMS) 2 was generated by adding 0.041 mL (1.0 mmol) of dry, degassed CH 3 OH to 0.29 mL (1.0 mmol) of P(TMS) 3 in 2.5 mL of THF.…”
Section: Materials and Methodologymentioning
confidence: 99%
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