Synthesis of both enantiomers of methylenolactocin, nephrosterinic acid and protolichesterinic acid via tandem aldol-lactonization reactions

Palangpon Kongsaeree; Puttinan Meepowpan; Yodhathai Thebtaranonth

doi:10.1016/S0957-4166(01)00345-7

Synthesis of both enantiomers of methylenolactocin, nephrosterinic acid and protolichesterinic acid via tandem aldol-lactonization reactions

Palangpon Kongsaeree
, Puttinan Meepowpan
, Yodhathai Thebtaranonth

Mahidol University
National Science and Technology Development Agency (NSTDA)

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

39 Citations (Scopus)

Abstract

Both forms of the enantiomerically pure methylenolactocin, nephrosterinic and protolichesterinic acid have been synthesized via tandem aldol-lactonization reactions from corresponding optically active itaconate-anthracene adducts.

Original language	English
Pages (from-to)	1913-1922
Number of pages	10
Journal	Tetrahedron Asymmetry
Volume	12
Issue number	13
DOIs	https://doi.org/10.1016/S0957-4166(01)00345-7
Publication status	Published - 30 Jul 2001
Externally published	Yes

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10.1016/S0957-4166(01)00345-7

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title = "Synthesis of both enantiomers of methylenolactocin, nephrosterinic acid and protolichesterinic acid via tandem aldol-lactonization reactions",

abstract = "Both forms of the enantiomerically pure methylenolactocin, nephrosterinic and protolichesterinic acid have been synthesized via tandem aldol-lactonization reactions from corresponding optically active itaconate-anthracene adducts.",

author = "Palangpon Kongsaeree and Puttinan Meepowpan and Yodhathai Thebtaranonth",

year = "2001",

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doi = "10.1016/S0957-4166(01)00345-7",

language = "English",

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journal = "Tetrahedron Asymmetry",

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T1 - Synthesis of both enantiomers of methylenolactocin, nephrosterinic acid and protolichesterinic acid via tandem aldol-lactonization reactions

AU - Kongsaeree, Palangpon

AU - Meepowpan, Puttinan

AU - Thebtaranonth, Yodhathai

PY - 2001/7/30

Y1 - 2001/7/30

N2 - Both forms of the enantiomerically pure methylenolactocin, nephrosterinic and protolichesterinic acid have been synthesized via tandem aldol-lactonization reactions from corresponding optically active itaconate-anthracene adducts.

AB - Both forms of the enantiomerically pure methylenolactocin, nephrosterinic and protolichesterinic acid have been synthesized via tandem aldol-lactonization reactions from corresponding optically active itaconate-anthracene adducts.

UR - https://www.scopus.com/pages/publications/0035973760

U2 - 10.1016/S0957-4166(01)00345-7

DO - 10.1016/S0957-4166(01)00345-7

M3 - Article

AN - SCOPUS:0035973760

SN - 0957-4166

VL - 12

SP - 1913

EP - 1922

JO - Tetrahedron Asymmetry

JF - Tetrahedron Asymmetry

IS - 13

ER -

Synthesis of both enantiomers of methylenolactocin, nephrosterinic acid and protolichesterinic acid via tandem aldol-lactonization reactions

Abstract

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