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- W2949164414 endingPage "3718" @default.
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- W2949164414 abstract "Under catalysis of Pd(OAc)2-(P-n-Bu)3, Et2Zn promotes a variety of allyl alcohols to undergo nucleophilic allylation of aliphatic aldehydes and ketones at room temperature and provides homoallyl alcohols in 60–90 and ca. 60% isolated yield, respectively. The reaction is irreversible and kinetically controlled, and unique regio- and stereoselectivities observed for the allylation with unsymmetrically substituted allyl alcohols are discussed." @default.
- W2949164414 created "2019-06-27" @default.
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- W2949164414 date "2005-04-01" @default.
- W2949164414 modified "2023-09-25" @default.
- W2949164414 title "Pd-catalyzed nucleophilic allylic alkylation of aliphatic aldehydes by the use of allyl alcohols" @default.
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- W2949164414 doi "https://doi.org/10.1016/j.tet.2005.02.005" @default.
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