Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
A New Method for the Preparation of 3, 4-Dihydro- and 1, 2, 3, 4-Tetrahydro-β-carbolines
AKIHIKO ISHIDATOHRU NAKAMURAKUNIHIKO IRIETOKURO OHISHI
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Keywords: Lawesson's reagent
JOURNAL FREE ACCESS

1985 Volume 33 Issue 8 Pages 3237-3249

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Abstract
N-Alkylthiocarbonyltryptophan (2a-i) and tryptamine (2j-m) derivatives can be converted into the corresponding 3, 4-dihydro-β-carbolines (3) under mild conditions by the use of alkylating or acylating agents. The NaBH4 reduction of 1, 3-disubstituted 3, 4-dihydro-β-carbolines (3a-i) gave cis- (5) or trans-1, 2, 3, 4-tetrahydro-β-carbolines (6) with satisfactory stereoselectivity. The synthesis of optically active 3a, b and 5a, b is also described.
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© The Pharmaceutical Society of Japan
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