@article{oai:kanazawa-u.repo.nii.ac.jp:00007390,
 author = {Segi, Masahito and Tanno, Katsuhiko and Kojima, Masumi and Honda, Mitsunori and Nakajima, Tadashi},
 issue = {13},
 journal = {Tetrahedron Letters},
 month = {Mar},
 note = {1,3-Dipolar cycloaddition between aromatic selenoaldehydes, generated by thermal retro Diels-Alder reaction of anthracene cycloadducts, and nitrile oxides or nitrile imines proceeded efficiently to give the corresponding [3+2] cycloadducts as a single isomer in good yields, being 1,4,2-oxaselenazoles or 1,3,4-selenadiazoles, respectively. © 2007 Elsevier Ltd. All rights reserved., 金沢大学大学院自然科学研究科物質創成, 金沢大学工学部},
 pages = {2303--2306},
 title = {An efficient 1,3-dipolar cycloaddition between aromatic selenoaldehydes and nitrile oxides or nitrile imines: an easy access to selenium-containing five-membered heterocyclic ring system},
 volume = {48},
 year = {2007}
}