Asymmetric organocatalysis: an enabling technology for medicinal chemistry
B Han, XH He, YQ Liu, G He, C Peng… - Chemical Society Reviews, 2021 - pubs.rsc.org
The efficacy and synthetic versatility of asymmetric organocatalysis have contributed
enormously to the field of organic synthesis since the early 2000s. As asymmetric …
enormously to the field of organic synthesis since the early 2000s. As asymmetric …
Targeting p53–MDM2 interaction by small-molecule inhibitors: Learning from MDM2 inhibitors in clinical trials
H Zhu, H Gao, Y Ji, Q Zhou, Z Du, L Tian… - Journal of hematology & …, 2022 - Springer
Abstract p53, encoded by the tumor suppressor gene TP53, is one of the most important
tumor suppressor factors in vivo and can be negatively regulated by MDM2 through p53 …
tumor suppressor factors in vivo and can be negatively regulated by MDM2 through p53 …
Stereoselective synthesis and applications of spirocyclic oxindoles
AJ Boddy, JA Bull - Organic Chemistry Frontiers, 2021 - pubs.rsc.org
The development of novel synthetic strategies to form new chemical entities in a
stereoselective manner is an ongoing significant objective in organic and medicinal …
stereoselective manner is an ongoing significant objective in organic and medicinal …
An overview of spirooxindole as a promising scaffold for novel drug discovery
LM Zhou, RY Qu, GF Yang - Expert Opinion on Drug Discovery, 2020 - Taylor & Francis
Introduction: Spirooxindole, a unique and versatile scaffold, has been widely studied in
some fields such as pharmaceutical chemistry and synthetic chemistry. Especially in the …
some fields such as pharmaceutical chemistry and synthetic chemistry. Especially in the …
[HTML][HTML] A guide to in silico drug design
Y Chang, BA Hawkins, JJ Du, PW Groundwater… - Pharmaceutics, 2023 - mdpi.com
The drug discovery process is a rocky path that is full of challenges, with the result that very
few candidates progress from hit compound to a commercially available product, often due …
few candidates progress from hit compound to a commercially available product, often due …
Spirooxindoles: Promising scaffolds for anticancer agents
The search for novel anticancer agents with more selectivity and lower toxicity continues to
be an area of intensive investigation. The unique structural features of spirooxindoles …
be an area of intensive investigation. The unique structural features of spirooxindoles …
Catalytic enantioselective construction of spiro quaternary carbon stereocenters
PW Xu, JS Yu, C Chen, ZY Cao, F Zhou, J Zhou - ACS Catalysis, 2019 - ACS Publications
The catalytic enantioselective assembly of spirocyclic molecules featuring a spiro quaternary
carbon stereocenter is currently of great interest because such privileged 3D structures are …
carbon stereocenter is currently of great interest because such privileged 3D structures are …
Isatins as privileged molecules in design and synthesis of spiro-fused cyclic frameworks
GS Singh, ZY Desta - Chemical Reviews, 2012 - ACS Publications
1. INTRODUCTION Indoline-2, 3-dione or indole-1H-2, 3-dione (Figure 1), commonly known
as isatin, is a well-known natural product found in plants of genus Isatis and in Couropita …
as isatin, is a well-known natural product found in plants of genus Isatis and in Couropita …
Therapeutic potential of spirooxindoles as antiviral agents
Antiviral therapeutics with profiles of high potency, low resistance, panserotype, and low
toxicity remain challenging, and obtaining such agents continues to be an active area of …
toxicity remain challenging, and obtaining such agents continues to be an active area of …
Organocatalytic asymmetric assembly reactions: synthesis of spirooxindoles via organocascade strategies
D Cheng, Y Ishihara, B Tan, CF Barbas III - Acs Catalysis, 2014 - ACS Publications
Spirooxindoles have become a privileged skeleton given their broad and promising
activities in various therapeutic areas. The strategies and catalyst systems described here …
activities in various therapeutic areas. The strategies and catalyst systems described here …