ChemInform Abstract: Thio‐Claisen Rearrangement Used in Preparing anti‐β‐Functionalized γ,δ‐Unsaturated Amino Acids: Scope and Limitations.

Liu, Zhihua; Mehta, Sukeshi J.; Lee, Kwang‐Soo; Grossman, Bryan; Qu, Hongchang; Gu, Xuyuan; Nichol, Gary S.; Hruby, Victor J.

doi:10.1002/chin.201222050

ChemInform

2012

DOI: 10.1002/chin.201222050

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ChemInform Abstract: Thio‐Claisen Rearrangement Used in Preparing anti‐β‐Functionalized γ,δ‐Unsaturated Amino Acids: Scope and Limitations.

Zhihua Liu

Sukeshi J. Mehta

Kwang‐Soo Lee

et al.

Abstract: FeBr3‐catalyzed or LDA‐mediated S‐alkylation of thioamides followed by thio‐Claisen rearrangement allows a regio‐, diastereo‐, and enantioselective access to the title compounds.

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ChemInform Abstract: Thio‐Claisen Rearrangement Used in Preparing anti‐β‐Functionalized γ,δ‐Unsaturated Amino Acids: Scope and Limitations.

Abstract: FeBr3‐catalyzed or LDA‐mediated S‐alkylation of thioamides followed by thio‐Claisen rearrangement allows a regio‐, diastereo‐, and enantioselective access to the title compounds.

Cited by 0 publications

References 1 publication

No citations

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