@article{cf7a34c575b24ea8ab3640ad6f949151,
title = "Asymmetric Synthesis of Functionalized 9-Methyldecalins Using a Diphenylprolinol-Silyl-Ether-Mediated Domino Michael/Aldol Reaction",
abstract = "Substituted 9-methyldecalin derivatives containing an all carbon quaternary chiral center were synthesized with excellent enantioselectivity via an organocatalyst-mediated domino reaction. The first reaction is a diphenylprolinol silyl ether-mediated Michael reaction, and the second reaction is an intramolecular aldol reaction. The enantiomerically pure catalyst is involved in both reactions.",
author = "Yujiro Hayashi and Salazar, {Hugo A.} and Seitaro Koshino",
note = "Funding Information: This work was supported by the Japan Society for the Promotion of Science (JSPS) Grants-in-Aid for Scientific Research (KAKENHI) Grant JP20H04801 in Hybrid Catalysis for Enabling Molecular Synthesis on Demand and JP19H05630. Hugo A. Salazar thanks the Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT) for financial support. Publisher Copyright: {\textcopyright} 2021 American Chemical Society.",
year = "2021",
month = sep,
day = "3",
doi = "10.1021/acs.orglett.1c02196",
language = "English",
volume = "23",
pages = "6654--6658",
journal = "Organic Letters",
issn = "1523-7060",
publisher = "American Chemical Society",
number = "17",
}