The recent impact of solid-phase synthesis on medicinally relevant benzoannelated nitrogen heterocycles

S Bräse, C Gil, K Knepper - Bioorganic & medicinal chemistry, 2002 - Elsevier
Benzoannelated heterocycles such as benzodiazepines and indoles can be prepared
efficiently through cyclization on solid supports, although no single approach is currently …

Inhibitors of cyclin-dependent kinases as anti-cancer therapeutics

PM Fischer, DP Lane - Current medicinal chemistry, 2000 - benthamdirect.com
Initiation, progression, and completion of the cell cycle are regulated by various cyclin-
dependent kinases (CDKs), which are thus critical for cell growth. Tumour development is …

Visible-Light-Promoted Selective Sulfonylation and Selenylation of Dienes to Access Sulfonyl-/Seleno-benzazepine Derivatives

Z Zhang, P Tan, S Wang, H Wang, L Xie, Y Chen… - Organic …, 2023 - ACS Publications
A novel visible-light-promoted selective sulfonylation and selenylation of dienes with
selenosulfonates has been developed. This technology provides mild access to a wide …

Paullones are potent inhibitors of glycogen synthase kinase‐3β and cyclin‐dependent kinase 5/p25

M Leost, C Schultz, A Link, YZ Wu… - European journal of …, 2000 - Wiley Online Library
Paullones constitute a new family of benzazepinones with promising antitumoral properties.
They were recently described as potent, ATP‐competitive, inhibitors of the cell cycle …

Rh (III)-Catalyzed annulative aldehydic CH functionalization for accessing ring-fluorinated benzo [b] azepin-5-ones

Q Li, K Yan, Y Zhu, G Qi, Y Wang, WJ Hao… - Chinese Chemical …, 2023 - Elsevier
A new Rh (III)-catalyzed aldehydic CH activation/[4+ 3] annulation cascade of N-sulfonyl-2-
aminobenzaldehydes with gem-difluorocyclopropenes is reported for the first time, and used …

Synthesis and biological evaluation of 1-phenyl-4, 6-dihydrobenzo [b] pyrazolo [3, 4-d] azepin-5 (1H)-one/thiones as anticancer agents

R Parupalli, R Akunuri, A Spandana… - Bioorganic …, 2023 - Elsevier
Cancer is associated with uncontrolled cell proliferation invading adjoining tissues and
organs. Despite the availability of several chemotherapeutic agents, the constant search for …

Iodine-mediated pyridine ring expansion for the construction of azepines

W Fan, S Xiang, Y Li, W Zhang, S Guo, D Huang - Organic Letters, 2022 - ACS Publications
A synthesis of azepines by the expansion of pyridine rings promoted by iodine in air is
reported. The scope of the method is demonstrated with 27 examples. Two iodinations are …

Fused-azepinones: Emerging scaffolds of medicinal importance

R Akunuri, M Vadakattu, S Bujji, V Veerareddy… - European Journal of …, 2021 - Elsevier
Hymenialdisine an alkaloid of oroidin class has drawn the attention of researchers owing to
its unique structural features and interesting biological properties. Hymenialdisine exhibited …

Development of pyridazine derivatives as potential EGFR inhibitors and apoptosis inducers: Design, synthesis, anticancer evaluation, and molecular modeling studies

MF Ahmed, EY Santali, EMM El-Deen, IA Naguib… - Bioorganic …, 2021 - Elsevier
Novel hybrids of pyridazine-pyrazoline were synthesized aiming to develop new
antiproliferative candidates. All compounds were submitted to the National Cancer Institute …

Mild, Metal-Free Oxidative Ring-Expansion Approach for the Synthesis of Benzo[b]azepines

S Stockerl, T Danelzik, DG Piekarski… - Organic …, 2019 - ACS Publications
Benzo [b] azepines are important structural motifs for the pharmaceutical industry. However,
their syntheses are usually lengthy, involving several steps, transition-metal catalysts, and/or …