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Journal
Publications |
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Rhodium-Catalyzed Double [2 + 2 + 2] Cycloaddition of
1,4-Bis(diphenylphosphinoyl)buta-1,3-diyne with Tethered Diynes: A
Modular, Highly Versatile Single-Pot Synthesis of NU-BIPHEP Biaryl
Diphosphines
Simon Doherty, Julian G.
Knight, Catherine H. Smyth, Ross W. Harrington, and William Clegg,
Org. Lett., 2007,
9, 4925. |
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Abstract:
Rhodium-catalyzed double [2 + 2 + 2]
cycloaddition of 1,4-bis(diphenylphosphinoyl)buta-1,3-diyne with
tethered diynes provides a straightforward, single-pot procedure for the
synthesis of a new class of tropos biaryl diphosphine, NU-BIPHEP. This
methodology represents a significant improvement on existing multistep
procedures. Enantiopure Lewis acid platinum complexes of these
diphosphines are highly efficient catalysts for carbonyl-ene and Diels-Alder
reactions, and ruthenium diphosphine-diamine complexes catalyze the
asymmetric reduction of ketones to give ee’s that rival those obtained
with their BINAP counterpart.
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