@article{oai:kutarr.kochi-tech.ac.jp:00000212,
 author = {Nishiwaki, Nagatoshi and Hirao, Shotaro and Sawayama, Jun and Saigo, Kazuhiko and Kobiro, Kazuya},
 journal = {Chemical Communications},
 month = {},
 note = {α-Nitro-δ-keto nitriles and α-nitro-δ-keto ester were readily converted to diazabicyclo compounds having vicinal functionality upon treatment with diamines. The keto nitrile attracts the diamine nearby to an acidic hydrogen to cause the pseudo-intramolecular imination which proceeds efficiently without any catalyst at room temperature.},
 pages = {4938--4940},
 title = {Bicyclization Involving Pseudo-Intramolecular Imination with Diamines},
 volume = {47},
 year = {2011}
}