Preparation of 1,2,3,4-tetrahydroisoquinolines lacking electron donating groups - An intramolecular cyclization complementary to the Pictet-Spengler reaction

DOI: 10.1016/0040-4039(96)01192-6

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Tetrahedron Letters p. 5453 - 5456 (1996)

Update date:2022-09-26

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Stokker

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Article abstract of DOI:10.1016/0040-4039(96)01192-6

The synthesis of 1,2,3,4-tetrahydroisoquinolines via an intramolecular cyclization of N-trifluoroacylated phenethylamines devoid of electron donating groups, with paraformaldehyde mediated by acetic/sulfuric acid milieu is described.

Full text of DOI:10.1016/0040-4039(96)01192-6

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Article Doi

Preparation of 1,2,3,4-tetrahydroisoquinolines lacking electron donating groups - An intramolecular cyclization complementary to the Pictet-Spengler reaction

DOI: 10.1016/0040-4039(96)01192-6

Source and publish data:

Authors:

Article abstract of DOI:10.1016/0040-4039(96)01192-6

Full text of DOI:10.1016/0040-4039(96)01192-6

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