Stereoselective total synthesis of (+)-lycoricidine

Noritaka Chida; Masami Ohtsuka; Seiichiro Ogawa

doi:10.1016/0040-4039(91)80030-A

Stereoselective total synthesis of (+)-lycoricidine

Noritaka Chida, Masami Ohtsuka, Seiichiro Ogawa

Department of Applied Chemistry

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

92 Citations (Scopus)

Abstract

The stereoselective total synthesis of the title compound starting from D-glucose is described. The key steps in this synthesis are Ferrier rearrangement to construct the optically active cyclohexenone (C-ring), and Pd-catalyzed intramolecular Heck reaction to build the phenanthridone skeleton.

Original language	English
Pages (from-to)	4525-4528
Number of pages	4
Journal	Tetrahedron Letters
Volume	32
Issue number	35
DOIs	https://doi.org/10.1016/0040-4039(91)80030-A
Publication status	Published - 1991

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/0040-4039(91)80030-A

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title = "Stereoselective total synthesis of (+)-lycoricidine",

abstract = "The stereoselective total synthesis of the title compound starting from D-glucose is described. The key steps in this synthesis are Ferrier rearrangement to construct the optically active cyclohexenone (C-ring), and Pd-catalyzed intramolecular Heck reaction to build the phenanthridone skeleton.",

author = "Noritaka Chida and Masami Ohtsuka and Seiichiro Ogawa",

year = "1991",

doi = "10.1016/0040-4039(91)80030-A",

language = "English",

volume = "32",

pages = "4525--4528",

journal = "Tetrahedron Letters",

issn = "0040-4039",

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T1 - Stereoselective total synthesis of (+)-lycoricidine

AU - Chida, Noritaka

AU - Ohtsuka, Masami

AU - Ogawa, Seiichiro

PY - 1991

Y1 - 1991

N2 - The stereoselective total synthesis of the title compound starting from D-glucose is described. The key steps in this synthesis are Ferrier rearrangement to construct the optically active cyclohexenone (C-ring), and Pd-catalyzed intramolecular Heck reaction to build the phenanthridone skeleton.

AB - The stereoselective total synthesis of the title compound starting from D-glucose is described. The key steps in this synthesis are Ferrier rearrangement to construct the optically active cyclohexenone (C-ring), and Pd-catalyzed intramolecular Heck reaction to build the phenanthridone skeleton.

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U2 - 10.1016/0040-4039(91)80030-A

DO - 10.1016/0040-4039(91)80030-A

M3 - Article

AN - SCOPUS:0025837981

SN - 0040-4039

VL - 32

SP - 4525

EP - 4528

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 35

ER -

Stereoselective total synthesis of (+)-lycoricidine

Abstract

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