Control of chemoselectivity in Dieckmann ring closures leading to tetramic acids

Yong Chul Jeong; Muhammad Anwar; Tuan Minh Nguyen; Benjamin Song Wei Tan; Christina Li Lin Chai; Mark G. Moloney

doi:10.1039/c1ob05816a

Control of chemoselectivity in Dieckmann ring closures leading to tetramic acids

Yong Chul Jeong
, Muhammad Anwar
, Tuan Minh Nguyen
, Benjamin Song Wei Tan
, Christina Li Lin Chai^*
, Mark G. Moloney

^*Corresponding author for this work

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

22 Citations (Scopus)

Abstract

An efficient strategy for the control of the chemoselectivity in Dieckmann ring closures leading to tetramic acids derived from serine and α-methyl serine is reported, and this provides pathways to diversely substituted systems from a common starting material.

Original language	English
Pages (from-to)	6663-6669
Number of pages	7
Journal	Organic and Biomolecular Chemistry
Volume	9
Issue number	19
DOIs	https://doi.org/10.1039/c1ob05816a
Publication status	Published - 7 Oct 2011
Externally published	Yes

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title = "Control of chemoselectivity in Dieckmann ring closures leading to tetramic acids",

abstract = "An efficient strategy for the control of the chemoselectivity in Dieckmann ring closures leading to tetramic acids derived from serine and α-methyl serine is reported, and this provides pathways to diversely substituted systems from a common starting material.",

author = "Jeong, \{Yong Chul\} and Muhammad Anwar and Nguyen, \{Tuan Minh\} and Tan, \{Benjamin Song Wei\} and Chai, \{Christina Li Lin\} and Moloney, \{Mark G.\}",

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AU - Jeong, Yong Chul

AU - Anwar, Muhammad

AU - Nguyen, Tuan Minh

AU - Tan, Benjamin Song Wei

AU - Chai, Christina Li Lin

AU - Moloney, Mark G.

PY - 2011/10/7

Y1 - 2011/10/7

N2 - An efficient strategy for the control of the chemoselectivity in Dieckmann ring closures leading to tetramic acids derived from serine and α-methyl serine is reported, and this provides pathways to diversely substituted systems from a common starting material.

AB - An efficient strategy for the control of the chemoselectivity in Dieckmann ring closures leading to tetramic acids derived from serine and α-methyl serine is reported, and this provides pathways to diversely substituted systems from a common starting material.

UR - https://www.scopus.com/pages/publications/80052708702

U2 - 10.1039/c1ob05816a

DO - 10.1039/c1ob05816a

M3 - Article

C2 - 21845281

AN - SCOPUS:80052708702

SN - 1477-0520

VL - 9

SP - 6663

EP - 6669

JO - Organic and Biomolecular Chemistry

JF - Organic and Biomolecular Chemistry

IS - 19

ER -

Control of chemoselectivity in Dieckmann ring closures leading to tetramic acids

Abstract

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