Concise synthesis of anolignan A

Meiming Luo; Akiko Matsui; Tomoyuki Esumi; Yoshiharu Iwabuchi; Susumi Hatakeyama

doi:10.1016/S0040-4039(00)00604-3

Concise synthesis of anolignan A

Meiming Luo, Akiko Matsui, Tomoyuki Esumi, Yoshiharu Iwabuchi, Susumi Hatakeyama

PHA - Molecular Pharmaceutical Science

Nagasaki University

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

11 Citations (Scopus)

Abstract

An efficient synthesis of anolignan A has been achieved in eight steps in 30% overall yield from piperonal employing TiCl₄-mediated addition of a 1-trimethylsilyl-2,3-butadiene to an aldehyde as the key step.

Original language	English
Pages (from-to)	4401-4402
Number of pages	2
Journal	Tetrahedron Letters
Volume	41
Issue number	22
DOIs	https://doi.org/10.1016/S0040-4039(00)00604-3
Publication status	Published - 2000 Jun 8

Keywords

1-trimethylsilyl-2,3-butadienes
Addition reactions
Lignans
Silicon compounds

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10.1016/S0040-4039(00)00604-3

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title = "Concise synthesis of anolignan A",

abstract = "An efficient synthesis of anolignan A has been achieved in eight steps in 30% overall yield from piperonal employing TiCl4-mediated addition of a 1-trimethylsilyl-2,3-butadiene to an aldehyde as the key step.",

keywords = "1-trimethylsilyl-2,3-butadienes, Addition reactions, Lignans, Silicon compounds",

author = "Meiming Luo and Akiko Matsui and Tomoyuki Esumi and Yoshiharu Iwabuchi and Susumi Hatakeyama",

note = "Funding Information: This work was supported by a JSPS postdoctoral fellowship for M.L. ",

year = "2000",

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doi = "10.1016/S0040-4039(00)00604-3",

language = "English",

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TY - JOUR

T1 - Concise synthesis of anolignan A

AU - Luo, Meiming

AU - Matsui, Akiko

AU - Esumi, Tomoyuki

AU - Iwabuchi, Yoshiharu

AU - Hatakeyama, Susumi

N1 - Funding Information: This work was supported by a JSPS postdoctoral fellowship for M.L.

PY - 2000/6/8

Y1 - 2000/6/8

N2 - An efficient synthesis of anolignan A has been achieved in eight steps in 30% overall yield from piperonal employing TiCl4-mediated addition of a 1-trimethylsilyl-2,3-butadiene to an aldehyde as the key step.

AB - An efficient synthesis of anolignan A has been achieved in eight steps in 30% overall yield from piperonal employing TiCl4-mediated addition of a 1-trimethylsilyl-2,3-butadiene to an aldehyde as the key step.

KW - 1-trimethylsilyl-2,3-butadienes

KW - Addition reactions

KW - Lignans

KW - Silicon compounds

UR - http://www.scopus.com/inward/record.url?scp=0034621972&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0034621972&partnerID=8YFLogxK

U2 - 10.1016/S0040-4039(00)00604-3

DO - 10.1016/S0040-4039(00)00604-3

M3 - Article

AN - SCOPUS:0034621972

SN - 0040-4039

VL - 41

SP - 4401

EP - 4402

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 22

ER -

Concise synthesis of anolignan A

Abstract

Keywords

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