TY - JOUR
T1 - Recent Advances in the Synthesis of Coumarin and Its Derivatives by Using Aryl Propiolates
AU - Sharma, Deepika
AU - Dhayalan, Vasudevan
AU - Chatterjee, Rana
AU - Khatravath, Mahender
AU - Dandela, Rambabu
N1 - Publisher Copyright:
© 2022 Wiley-VCH GmbH
PY - 2022/1/27
Y1 - 2022/1/27
N2 - Coumarins (2H-1-benzopyran-2-one) are a class of natural products extracted from plant with a broad range of biological activities like antitubercular, anti-inflammatory, anticancer, anticonvulsant, neuroprotective, antiviral, antifungal, antibacterial, antihyperglycemic, anticoagulant, antihypertensive, antiadipogenic, and antioxidant, effects. Therefore, the synthesis of coumarin and its derivatives has become amongst the most attractive compounds over the last two decades in the growth of improved synthetic methods to form various coumarins derivatives. Amongst the reported methods for the construction of coumarins, the pendant arylpropiolate scaffolds served as a highly appealing precursor for coumarins in a single step. This review article describes recent updates on the construction of coumarins using arylpropiolate as substrates.
AB - Coumarins (2H-1-benzopyran-2-one) are a class of natural products extracted from plant with a broad range of biological activities like antitubercular, anti-inflammatory, anticancer, anticonvulsant, neuroprotective, antiviral, antifungal, antibacterial, antihyperglycemic, anticoagulant, antihypertensive, antiadipogenic, and antioxidant, effects. Therefore, the synthesis of coumarin and its derivatives has become amongst the most attractive compounds over the last two decades in the growth of improved synthetic methods to form various coumarins derivatives. Amongst the reported methods for the construction of coumarins, the pendant arylpropiolate scaffolds served as a highly appealing precursor for coumarins in a single step. This review article describes recent updates on the construction of coumarins using arylpropiolate as substrates.
UR - http://www.scopus.com/inward/record.url?scp=85123760659&partnerID=8YFLogxK
U2 - 10.1002/slct.202104299
DO - 10.1002/slct.202104299
M3 - Review article
AN - SCOPUS:85123760659
SN - 2365-6549
VL - 7
JO - ChemistrySelect
JF - ChemistrySelect
IS - 4
M1 - e202104299
ER -