Syntheses of (±)-thuriferic acid ethyl ester, its analogues and (±)-picropodophyllone

Manat Pohmakotr; Taweechote Komutkul; Patoomratana Tuchinda; Samrarn Prabpai; Palangpon Kongsaeree; Vichai Reutrakul

doi:10.1016/j.tet.2005.03.069

Syntheses of (±)-thuriferic acid ethyl ester, its analogues and (±)-picropodophyllone

Manat Pohmakotr
, Taweechote Komutkul
, Patoomratana Tuchinda
, Samrarn Prabpai
, Palangpon Kongsaeree
, Vichai Reutrakul

Mahidol University

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

15 Citations (Scopus)

Abstract

(±)-Thuriferic acid ethyl ester, its analogues as well as (±)-picropodophyllone have been prepared. The synthetic strategy is based on the utility of vicinal dianions derived from α-aroylsuccinic esters.

Original language	English
Pages (from-to)	5311-5321
Number of pages	11
Journal	Tetrahedron
Volume	61
Issue number	22
DOIs	https://doi.org/10.1016/j.tet.2005.03.069
Publication status	Published - 30 May 2005
Externally published	Yes

Keywords

Picropodophyllone
Vicinal dianion
α-Aroylparaconic ester
α-Aroylsuccinic ester

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10.1016/j.tet.2005.03.069

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title = "Syntheses of (±)-thuriferic acid ethyl ester, its analogues and (±)-picropodophyllone",

abstract = "(±)-Thuriferic acid ethyl ester, its analogues as well as (±)-picropodophyllone have been prepared. The synthetic strategy is based on the utility of vicinal dianions derived from α-aroylsuccinic esters.",

keywords = "Picropodophyllone, Vicinal dianion, α-Aroylparaconic ester, α-Aroylsuccinic ester",

author = "Manat Pohmakotr and Taweechote Komutkul and Patoomratana Tuchinda and Samrarn Prabpai and Palangpon Kongsaeree and Vichai Reutrakul",

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T1 - Syntheses of (±)-thuriferic acid ethyl ester, its analogues and (±)-picropodophyllone

AU - Pohmakotr, Manat

AU - Komutkul, Taweechote

AU - Tuchinda, Patoomratana

AU - Prabpai, Samrarn

AU - Kongsaeree, Palangpon

AU - Reutrakul, Vichai

PY - 2005/5/30

Y1 - 2005/5/30

N2 - (±)-Thuriferic acid ethyl ester, its analogues as well as (±)-picropodophyllone have been prepared. The synthetic strategy is based on the utility of vicinal dianions derived from α-aroylsuccinic esters.

AB - (±)-Thuriferic acid ethyl ester, its analogues as well as (±)-picropodophyllone have been prepared. The synthetic strategy is based on the utility of vicinal dianions derived from α-aroylsuccinic esters.

KW - Picropodophyllone

KW - Vicinal dianion

KW - α-Aroylparaconic ester

KW - α-Aroylsuccinic ester

UR - https://www.scopus.com/pages/publications/18844390987

U2 - 10.1016/j.tet.2005.03.069

DO - 10.1016/j.tet.2005.03.069

M3 - Article

AN - SCOPUS:18844390987

SN - 0040-4020

VL - 61

SP - 5311

EP - 5321

JO - Tetrahedron

JF - Tetrahedron

IS - 22

ER -

Syntheses of (±)-thuriferic acid ethyl ester, its analogues and (±)-picropodophyllone

Abstract

Keywords

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