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ChemInform Abstract: Highly Efficient Photochemical Addition of Tertiary Amines to Electron-Deficient Alkenes. Diastereoselective Addition to (5R)-5-Menthyloxy-2[5H]-furanone.

✍ Scribed by Samuel Bertrand; Cedric Glapski; Norbert Hoffmann; Jean-Pierre Pete

Publisher
John Wiley and Sons
Year
2010
Weight
32 KB
Volume
30
Category
Article
ISSN
0931-7597

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ChemInform Abstract: Stereoselective Rad
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Application to the Enantioselective Synthesis of (-)-Isoretronecanol and (+)-Laburnine. -Compound (I) is an adduct of a stereoselective radical addition of a tertiary amine with (5R)-5-menthyloxy-2[5H]-furanone. It is readily transformed to (+)-laburnine (IV) in a three-step sequence. Similarly, (-

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ChemInform Abstract: Highly Efficient and Stereoselective Radical Addition of Tertiary Amines to Electron-Deficient Alkenes β€” Application to the Enantioselective Synthesis of Necine Bases.
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v