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Stereo- and Regioselective Synthesis of 4-Vinylpyrrolidine from N-Tethered Alkyne-Alkenol.

ABSTRACT: Indium(III) chloride can be efficiently used for the synthesis of 4-vinylpyrrolidine from N-tethered alkyne-alkenol in good yields. The reaction is highly stereo- and regioselective.

SUBMITTER: Devi NR

PROVIDER: S-EPMC6641446 | biostudies-literature | 2018 Jan

REPOSITORIES: biostudies-literature

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Stereo- and Regioselective Synthesis of 4-Vinylpyrrolidine from N-Tethered Alkyne-Alkenol.

Devi Ngangbam Renubala NR Behera Bipin K BK Saikia Anil K AK

ACS omega 20180118 1

Indium(III) chloride can be efficiently used for the synthesis of 4-vinylpyrrolidine from N-tethered alkyne-alkenol in good yields. The reaction is highly stereo- and regioselective. ...[more]

PMID: 31457915

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