A specific and efficient synthesis of (±)-dihydrocorynantheol (1) is reported. Starting with the easily accessible imine (3), ring D was built via stereoselective reaction with the lactone (4a), thus providing the complete carbon skeleton of (1); subsequent elaboration gave the desired alkaloid (1).

A specific and efficient synthesis of (±)-dihydrocorynantheol / B. Danieli, G. Lesma, G. Palmisano, S. Tollari. - In: JOURNAL OF THE CHEMICAL SOCIETY. PERKIN TRANSACTIONS. I. - ISSN 0300-922X. - :0(1984), pp. 1237-1240. [10.1039/P19840001237]

A specific and efficient synthesis of (±)-dihydrocorynantheol

B. Danieli
Primo
;
G. Lesma
Secondo
;
1984

Abstract

A specific and efficient synthesis of (±)-dihydrocorynantheol (1) is reported. Starting with the easily accessible imine (3), ring D was built via stereoselective reaction with the lactone (4a), thus providing the complete carbon skeleton of (1); subsequent elaboration gave the desired alkaloid (1).
Settore CHIM/06 - Chimica Organica
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/2434/183790
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