Repozytorium

Stereoselective addition of dialkyl phosphites to di-salicylaldimines bearing the (R,R)-1,2-diaminocyclohexane moiety.

Autorzy

Jarosław Lewkowski

Paweł Tokarz

Tadeusz Lis

Katarzyna Ślepokura

Rok wydania

2014

Czasopismo

Tetrahedron

Numer woluminu

70

Strony

810-816

DOI

10.1016/j.tet.2013.12.042

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

The addition of dialkyl phosphites to the azomethine bond of N,N′-disalicylidene-1,2-diaminocyclohexane imines, catalyzed by sodium hydride led to bis-aminophosphonates in a high diastereoselectivity. One of the bis-aminophosphonates was analyzed by X-ray diffraction. Another bis-aminophosphonate was converted to a bis-aminophosphonic acid and the structure was studied by X-ray diffraction. Addition of phosphites to a diimine resulted in an aminophosphonate, which was also studied by X-ray diffraction. An explanation of the diastereoselectivity is suggested.

Słowa kluczowe

Aza-Pudovik reaction, Stereoselectivity, atom, 2-Diaminocyclohexane, Aminophosphonates

Adres publiczny

http://dx.doi.org/10.1016/j.tet.2013.12.042

Strona internetowa wydawcy

http://www.elsevier.com

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