том 12 издание 6

Recent Advances in Indole Synthesis and the Related Alkylation

Тип публикацииJournal Article
Дата публикации2023-05-12
scimago Q2
wos Q2
БС1
SJR0.542
CiteScore5.0
Impact factor2.7
ISSN21935807, 21935815
Organic Chemistry
Краткое описание

The derivatives of indoles are very useful intermediates in pharmaceuticals and organic synthesis. The efficient synthesis of the indole blocks and related functionalizations, especially the alkylation of indoles are hot topics in recent years. This review will focus on the following two aspects: i) new developments for the synthesis of indoles which was catalyzed by transition metals, the alkylation of indoles, including the one on N1‐position, C2‐position, as well as C3‐position. 1. Introduction 2. Synthesis of indoles catalyzed by various metals 2.1. Synthesis of indoles by palladium catalysts 2.2. Synthesis of indoles by other metal catalysts 3. Alkylation of indoles 3.1. N1‐alkylation of indoles 3.2. C2‐alkylation of indoles 3.3. C3‐alkylation of indoles

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ГОСТ |
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Ma J. et al. Recent Advances in Indole Synthesis and the Related Alkylation // Asian Journal of Organic Chemistry. 2023. Vol. 12. No. 6.
ГОСТ со всеми авторами (до 50) Скопировать
Ma J., FENG RONG, Dong Z. Recent Advances in Indole Synthesis and the Related Alkylation // Asian Journal of Organic Chemistry. 2023. Vol. 12. No. 6.
RIS |
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TY - JOUR
DO - 10.1002/ajoc.202300092
UR - https://doi.org/10.1002/ajoc.202300092
TI - Recent Advances in Indole Synthesis and the Related Alkylation
T2 - Asian Journal of Organic Chemistry
AU - Ma, Jie
AU - FENG RONG
AU - Dong, Zhibing
PY - 2023
DA - 2023/05/12
PB - Wiley
IS - 6
VL - 12
SN - 2193-5807
SN - 2193-5815
ER -
BibTex
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BibTex (до 50 авторов) Скопировать
@article{2023_Ma,
author = {Jie Ma and FENG RONG and Zhibing Dong},
title = {Recent Advances in Indole Synthesis and the Related Alkylation},
journal = {Asian Journal of Organic Chemistry},
year = {2023},
volume = {12},
publisher = {Wiley},
month = {may},
url = {https://doi.org/10.1002/ajoc.202300092},
number = {6},
doi = {10.1002/ajoc.202300092}
}