Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/163038
Title: Synthesis of penicolinates A, C and D
Authors: Chiu, Angela Qi Yun
Krishna, Ramesh
Phyo, Ma Yadanar
Sae-Lao, Patcharaporn
Bates, Roderick Wayland
Keywords: Science::Chemistry
Issue Date: 2022
Source: Chiu, A. Q. Y., Krishna, R., Phyo, M. Y., Sae-Lao, P. & Bates, R. W. (2022). Synthesis of penicolinates A, C and D. Heterocycles, 105(1), 588-593. https://dx.doi.org/10.3987/COM-22-S(R)15
Project: NRF–CRP18–2017–01
Journal: Heterocycles
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).
URI: https://hdl.handle.net/10356/163038
ISSN: 1881-0942
DOI: 10.3987/COM-22-S(R)15
Rights: © 2022 The Japan Institute of Heterocyclic Chemistry. All rights reserved.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SPMS Journal Articles

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