SYNTHESIS OF PENICOLINATES A, C AND D

Angela Qi Yun Chiu; Krishna Ramesh; Ma Yadanar Phyo; Patcharaporn Sae-Lao; Roderick Wayland Bates

doi:10.3987/COM-22-S(R)15

SYNTHESIS OF PENICOLINATES A, C AND D

Angela Qi Yun Chiu, Krishna Ramesh, Ma Yadanar Phyo, Patcharaporn Sae-Lao, Roderick Wayland Bates^*

^*Corresponding author for this work

Nanyang Technological University

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

Abstract

Penicolinates A, C and D are synthesized using the Sonogashira coupling reaction as a key step. By comparison of the optical rotation, the stereochemistry of penicolinate D is determined to be (S).

Original language	English
Pages (from-to)	588-593
Number of pages	6
Journal	Heterocycles
Volume	105
Issue number	1
DOIs	https://doi.org/10.3987/COM-22-S(R)15
Publication status	Published - 2022
Externally published	Yes

Bibliographical note

Publisher Copyright:
© 2022 The Japan Institute of Heterocyclic Chemistry.

ASJC Scopus Subject Areas

Analytical Chemistry
Pharmacology
Organic Chemistry

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Cite this

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title = "SYNTHESIS OF PENICOLINATES A, C AND D",

abstract = "Penicolinates A, C and D are synthesized using the Sonogashira coupling reaction as a key step. By comparison of the optical rotation, the stereochemistry of penicolinate D is determined to be (S).",

author = "Chiu, {Angela Qi Yun} and Krishna Ramesh and Phyo, {Ma Yadanar} and Patcharaporn Sae-Lao and Bates, {Roderick Wayland}",

note = "Publisher Copyright: {\textcopyright} 2022 The Japan Institute of Heterocyclic Chemistry.",

year = "2022",

doi = "10.3987/COM-22-S(R)15",

language = "English",

volume = "105",

pages = "588--593",

journal = "Heterocycles",

issn = "0385-5414",

publisher = "Japan Institute of Heterocyclic Chemistry",

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T1 - SYNTHESIS OF PENICOLINATES A, C AND D

AU - Chiu, Angela Qi Yun

AU - Ramesh, Krishna

AU - Phyo, Ma Yadanar

AU - Sae-Lao, Patcharaporn

AU - Bates, Roderick Wayland

PY - 2022

Y1 - 2022

N2 - Penicolinates A, C and D are synthesized using the Sonogashira coupling reaction as a key step. By comparison of the optical rotation, the stereochemistry of penicolinate D is determined to be (S).

AB - Penicolinates A, C and D are synthesized using the Sonogashira coupling reaction as a key step. By comparison of the optical rotation, the stereochemistry of penicolinate D is determined to be (S).

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U2 - 10.3987/COM-22-S(R)15

DO - 10.3987/COM-22-S(R)15

M3 - Article

AN - SCOPUS:85133860238

SN - 0385-5414

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JO - Heterocycles

JF - Heterocycles

IS - 1

ER -

SYNTHESIS OF PENICOLINATES A, C AND D

Abstract

Bibliographical note

ASJC Scopus Subject Areas

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