@article{2cef018bcc704fee995a3d658842e527,
title = "Synthesis of tetrahydrochromenes and dihydronaphthofurans via a cascade process of [3 + 3] and [3 + 2] annulation reactions: mechanistic insight for 6-endo-trig and 5-exo-trig cyclisation",
abstract = "Substituted tetrahydrochromenes and dihydronaphthofurans are easily accessible by the treatment of β-tetralone with trans-β-nitro styrene derived Morita-Baylis-Hillman (MBH) acetates through a formal [3 + 3]/[3 + 2] annulation. The reaction proceeds through a cascade Michael/oxa-Michael pathway with moderate to good yields. A DFT study was carried out to account for the formation of the corresponding six and five-membered heterocycles via 6-endo-trig and 5-exo-trig cyclization.",
author = "Reddy, {Yeruva Pavankumar} and V. Srinivasadesikan and Rengarajan Balamurugan and Lin, {M. C.} and Shaik Anwar",
note = "Publisher Copyright: {\textcopyright} 2023 The Royal Society of Chemistry.",
year = "2023",
month = feb,
day = "16",
doi = "10.1039/d2ra08163f",
language = "English",
volume = "13",
pages = "5796--5803",
journal = "RSC Advances",
issn = "2046-2069",
publisher = "Royal Society of Chemistry",
number = "9",
}