A tandem Horner-Emmons olefination-conjugate addition approach to the synthesis of 1,5- disubstituted-6-azabicyclo[3.2.1]octanes based on the AE ring structure of the norditerpenoid alkaloid methyllycaconitine

Thomas, Noel F. (1996) A tandem Horner-Emmons olefination-conjugate addition approach to the synthesis of 1,5- disubstituted-6-azabicyclo[3.2.1]octanes based on the AE ring structure of the norditerpenoid alkaloid methyllycaconitine. pp. 4634-4640.

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Item Type: Article
Uncontrolled Keywords: A tandem Horner-Emmons olefination-conjugate addition approach to the synthesis of 1,5- disubstitut
Subjects: Q Science
Depositing User: MR. ADNAN YAHYA
Last Modified: 23 Apr 2013
URI: http://repository.um.edu.my/id/eprint/1753

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