An unusual by-product in a concise synthesis of a rotationally restricted phenolic analog of serotonin

DOI: 10.1016/0040-4039(95)01453-O

Source and publish data:

Tetrahedron Letters p. 7019 - 7022 (1995)

Update date:2022-08-11

Topics:: Authors:

Macor, John E.

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Article abstract of DOI:10.1016/0040-4039(95)01453-O

An improved synthesis of a dihydropyrano[3,-2e]indole analog (4, CP-123,479) of serotonin has been accomplished. Starting with serotonin itself and utilizing a Claisen rearrangement/cyclization of a 5-propargyloxy-N-Cbz-tryptamine (2) to form the pyrano[3

Full text of DOI:10.1016/0040-4039(95)01453-O

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An unusual by-product in a concise synthesis of a rotationally restricted phenolic analog of serotonin

DOI: 10.1016/0040-4039(95)01453-O

Source and publish data:

Authors:

Article abstract of DOI:10.1016/0040-4039(95)01453-O

Full text of DOI:10.1016/0040-4039(95)01453-O

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