[2:1] and [2:2] cycloadducts from N-sulfonylamines and azomethines

Autor:	Andreas Lender, Ernst Schaumann, Nigel P. C. Walker
Rok vydání:	2015
Předmět:	Steric effects Stereochemistry Chemistry Organic Chemistry Drug Discovery Biochemistry Cycloaddition
Zdroj:	Tetrahedron Letters. 56:4800-4803
ISSN:	0040-4039
Popis:	The title compounds react to give [2:1] cycloadducts with a dithiatriazine structure. However, the least sterically hindered sulfonylamine and a 3,4-dihydroisoquinoline react in a highly unusual [4+4] cycloaddition.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::39422b01295d990b9e8e400efd070bf6 https://doi.org/10.1016/j.tetlet.2015.06.060 Zobrazit plný text záznamu Full Text from ScienceDirect