 trans-Hydroalumination/Alkylation: One-Pot Synthesis of Trisubstituted Allylic Alcohols by Neil F. Langille and Timothy F. Jamison

ID: trans-hydroalumination-alkylation-one-pot-synthesis-of-trisubstituted-allylic-alcohols-by-neil-f-langille-and-timothy-f-jamison

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trans-Hydroalumination/Alkylation: One-Pot Synthesis of Trisubstituted Allylic Alcohols by Neil F. Langille and Timothy F. Jamison by

Codex  0 2026-10-20

doi.org/10.1021/ol0613721

Organic Letters 8, 3761–3764. Red-Al converts propargylic alcohols to alkenyl alanates that can be intercepted by electrophiles; this supports a directed trans-hydroalumination intermediate.

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