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- W1992984512 abstract "Abstract Tertiary amines derived from pyrrolidines can be added very efficiently (isolated yields up to 94%) to (5R)-5-mentyloxy-2[5H]-furanone. The addition, which follows a radical chain mechanism initiated by a photoinitiated electron transfer (PET) from the tertiary amine to the excited aromatic ketone, occurs with a complete facial selectivity on the furanone ring. The method can be generalized to the addition of tertiary amines and N-protected secondary amines to electron deficient alkenes." @default.
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- W1992984512 date "2010-06-14" @default.
- W1992984512 modified "2023-10-18" @default.
- W1992984512 title "ChemInform Abstract: Highly Efficient Photochemical Addition of Tertiary Amines to Electron-Deficient Alkenes. Diastereoselective Addition to (5R)-5-Menthyloxy-2[5H]-furanone." @default.
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- W1992984512 doi "https://doi.org/10.1002/chin.199929113" @default.
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