A biomimetic route to the ergot derailment products, the clavicipitic acids - detection of a reactive intermediate by 31p nmr - some chemical underpinnings for a proposed intermediate in ergot alkaloid biosynthesis.

Alan P. Kozikowski; Makoto Okita

doi:10.1016/S0040-4039(00)89288-6

A biomimetic route to the ergot derailment products, the clavicipitic acids - detection of a reactive intermediate by ³¹p nmr - some chemical underpinnings for a proposed intermediate in ergot alkaloid biosynthesis.

Alan P. Kozikowski
, Makoto Okita

School of Medicine

Research output: Contribution to journal › Article › peer-review

15 Scopus citations

Abstract

A biomimetic route to the clavicipitic acids has been developed which is based on the Mitsunobu reaction of the diol 4a.

Original language	English (US)
Pages (from-to)	4043-4046
Number of pages	4
Journal	Tetrahedron Letters
Volume	26
Issue number	34
DOIs	https://doi.org/10.1016/S0040-4039(00)89288-6
State	Published - 1985

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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A biomimetic route to the ergot derailment products, the clavicipitic acids - detection of a reactive intermediate by ³¹p nmr - some chemical underpinnings for a proposed intermediate in ergot alkaloid biosynthesis. / Kozikowski, Alan P.; Okita, Makoto.
In: Tetrahedron Letters, Vol. 26, No. 34, 1985, p. 4043-4046.

Research output: Contribution to journal › Article › peer-review

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