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- W2961029520 endingPage "12496" @default.
- W2961029520 startingPage "12491" @default.
- W2961029520 abstract "An enantioselective sulfenylation/semipinacol rearrangement of 1,1-disubstituted and trisubstituted allylic alcohols was accomplished with a chiral Lewis base and a chiral Brønsted acid as cocatalysts, generating various β-arylthio ketones bearing an all-carbon quaternary center in moderate to excellent yields and excellent enantioselectivities. These chiral arylthio ketone products are common intermediates with many applications, for example, in the design of new chiral catalysts/ligands and the total synthesis of natural products. Computational studies (DFT calculations) were carried out to explain the enantioselectivity and the role of the chiral Brønsted acid. Additionally, the synthetic utility of this method was exemplified by an enantioselective total synthesis of (−)-herbertene and a one-pot synthesis of a chiral sulfoxide and sulfone." @default.
- W2961029520 created "2019-07-23" @default.
- W2961029520 creator A5001134518 @default.
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- W2961029520 creator A5077722126 @default.
- W2961029520 creator A5091437021 @default.
- W2961029520 date "2019-09-02" @default.
- W2961029520 modified "2023-10-14" @default.
- W2961029520 title "Lewis Base/Brønsted Acid Co‐catalyzed Enantioselective Sulfenylation/Semipinacol Rearrangement of Di‐ and Trisubstituted Allylic Alcohols" @default.
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