@article{d28b9d5f62b24cf7971fe0c56d259a3a,
title = "Highly enantioselective preparation of tricyclo[4.4.0.05,7]decene derivatives via catalytic asymmetric intramolecular cyclopropanation reactions of α-diazo-β-keto esters",
abstract = "The enantioselective preparation of the tricyclo[4.4.0.05,7]dec-2-ene derivatives via the catalytic asymmetric intramolecular cyclopropanation (CAIMCP) reactions of α-diazo-β-keto esters with excellent ee (95-98% ee) is described. The chiral building blocks reported herein would be versatile intermediates for enantioselective natural products synthesis.",
author = "Ryoji Ida and Masahisa Nakada",
note = "Funding Information: This work was financially supported in part by a Waseda University Grant for Special Research Projects and a Grant-in-Aid for Scientific Research on Priority Areas (Creation of Biologically Functional Molecules (No. 17035082)) from the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan. We are also indebted to 21COE {\textquoteleft}Practical Nano-Chemistry{\textquoteright}.",
year = "2007",
month = jul,
day = "9",
doi = "10.1016/j.tetlet.2007.05.046",
language = "English",
volume = "48",
pages = "4855--4859",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier Limited",
number = "28",
}