TY  - JOUR
AU  - Gao, Jie
AU  - Li, Xiaohan
AU  - Liu, Xinye
AU  - Mei, Zhiyang
AU  - Dan, Mingxia
AU  - Zhan, Wei
AU  - Zheng, Shaojun
AU  - Zhu, Rui
TI  - Synthesis and structure–activity relationship of β -carboline derivatives with antifungal activity
JF  - NATURAL PRODUCT RESEARCH
J2  - NAT PROD RES
VL  - 2025
PY  - 2025
SP  - 1
EP  - 9
PG  - 9
SN  - 1478-6419
DO  - 10.1080/14786419.2025.2502853
UR  - https://m2.mtmt.hu/api/publication/36158854
ID  - 36158854
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Li, Cuiying
AU  - Yang, Haiyun
AU  - Kang, Honglan
AU  - Lv, Xin
TI  - Synthesis of Carboline Derivatives Using Domino Annulation Strategies
JF  - ADVANCED SYNTHESIS & CATALYSIS
J2  - ADV SYNTH CATAL
VL  - 17 Dec
PY  - 2025
SN  - 1615-4150
DO  - 10.1002/adsc.70146
UR  - https://m2.mtmt.hu/api/publication/36559779
ID  - 36559779
AB  - Carbolines represent a class of privileged heterocyclic scaffolds that widely exist in natural products, pharmaceutical agents, agrochemicals, and functional materials. Despite their importance, the development of facile and efficient methods for synthesizing carboline derivatives remains a pivotal challenge in modern organic synthesis and heterocyclic chemistry. Domino annulation has evolved as a powerful strategy enabling convenient assembly of diverse heterocyclic molecules. Significant progress has been achieved in this field during recent years. This review highlights the important developments in the novel domino annulations for carboline synthesis since 2019. It aims to provide a valuable resource for organic researchers, offering deeper insights into the reactivity and synthetic potential of these elegant methods. It is also hoped that this review will inspire development of novel domino annulation strategies, thereby expanding the toolbox for N‐heterocycle synthesis.
LA  - English
DB  - MTMT
ER  - 

TY  - JOUR
AU  - Selka, A.
AU  - Abidli, A.
AU  - Schiavo, L.
AU  - Jeanmart, L.
AU  - Hanquet, G.
AU  - Lubell, W.D.
TI  - Recent Advances in Sustainable Total Synthesis and Chiral Pool Strategies with Emphasis on (−)-Sclareol in Natural Products Synthesis
JF  - EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
J2  - EUR J ORG CHEM
VL  - 28
PY  - 2025
IS  - 8
SN  - 1434-193X
DO  - 10.1002/ejoc.202400983
UR  - https://m2.mtmt.hu/api/publication/35781554
ID  - 35781554
LA  - English
DB  - MTMT
ER  -