том 42 страницы 101798

Xylochemical synthesis of diarylated heterocycles

Тип публикацииJournal Article
Дата публикации2024-12-01
scimago Q1
wos Q1
БС1
SJR0.966
CiteScore8.8
Impact factor5.8
ISSN23525541
Краткое описание
The production of (hetero)aromatic fine chemicals heavily relies on base chemicals sourced from petroleum. The concept of xylochemistry focuses on using compounds derived from wood and other plant materials as building blocks for chemical synthesis, thereby reducing our dependence on fossil carbon. In this study, we demonstrate that the xylochemical apocynin can be readily converted into several diarylated heterocycles that resemble molecules of interest in medicinal, materials, and natural product chemistry. In all cases, the heteroatoms (O, N, S) can be sourced from biorenewable resources and as a result, every atom in all the products can be considered biogenic.
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Millar S. B. et al. Xylochemical synthesis of diarylated heterocycles // Sustainable Chemistry and Pharmacy. 2024. Vol. 42. p. 101798.
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Millar S. B., Khachatryan H. N., Malmir M., Sperry J. Xylochemical synthesis of diarylated heterocycles // Sustainable Chemistry and Pharmacy. 2024. Vol. 42. p. 101798.
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TY - JOUR
DO - 10.1016/j.scp.2024.101798
UR - https://linkinghub.elsevier.com/retrieve/pii/S2352554124003735
TI - Xylochemical synthesis of diarylated heterocycles
T2 - Sustainable Chemistry and Pharmacy
AU - Millar, Stephanie B.
AU - Khachatryan, Hasmik N
AU - Malmir, Masoume
AU - Sperry, Jonathan
PY - 2024
DA - 2024/12/01
PB - Elsevier
SP - 101798
VL - 42
SN - 2352-5541
ER -
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@article{2024_Millar,
author = {Stephanie B. Millar and Hasmik N Khachatryan and Masoume Malmir and Jonathan Sperry},
title = {Xylochemical synthesis of diarylated heterocycles},
journal = {Sustainable Chemistry and Pharmacy},
year = {2024},
volume = {42},
publisher = {Elsevier},
month = {dec},
url = {https://linkinghub.elsevier.com/retrieve/pii/S2352554124003735},
pages = {101798},
doi = {10.1016/j.scp.2024.101798}
}