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• W2081521474 abstract "We report the first example of a coupling reaction of chiral secondary boronic esters generated by the hydroboration of vinyl arenes. In order for the reaction to take place in high yields, the use of silver oxide as a base and the presence of at least 8 equiv of triphenyl phosphine per Pd are required. The reaction proceeds with >90% retention of configuration in all cases except one. Remarkably, the linear boronate ester does not react under these conditions." @default.
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• W2081521474 date "2009-03-20" @default.
• W2081521474 modified "2023-10-06" @default.
• W2081521474 title "Cross Coupling Reactions of Chiral Secondary Organoboronic Esters With Retention of Configuration" @default.
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• W2081521474 doi "https://doi.org/10.1021/ja8094075" @default.
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• W2081521474 hasPublicationYear "2009" @default.
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