A concise route to a key intermediate in the total synthesis of sempervirine

Article abstract of DOI:10.1080/00397919608003843

Diels-Alder reaction of 5-acetyl-3-methylthio-1,2,4-triazine 3 with 1-pyrrolidino-1-cyclohexene afforded 3-acetyl-1-methylthio-5,6,7,8-tetrahydroisoquinoline 4 which was readily converted into target 2-(3-(5,6,7,8-tetrahydroisoquinolinyl)indole 6 via Fish

Full text of DOI:10.1080/00397919608003843

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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A Concise Route to a Key
Intermediate in the Total
Synthesis of Sempervirine1
Andrzej Rykowski a & Teodozja Lipińska a
a Institute of Chemistry, Agricultural University at
Sicdlcc, 08–110, Sicdlce, Poland
Published online: 23 Aug 2006.
To cite this article: Andrzej Rykowski & Teodozja Lipińska (1996): A Concise
Route to a Key Intermediate in the Total Synthesis of Sempervirine1 , Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 26:23, 4409-4414
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