Title of article :
Expeditious N-monoalkylation of 1,4,7,10-tetraazacyclododecane (cyclen) via formamido protection
Author/Authors :
Boldrini، نويسنده , , Vincenzo and Giovenzana، نويسنده , , Giovanni B and Pagliarin، نويسنده , , Roberto and Palmisano، نويسنده , , Giovanni and Sisti، نويسنده , , Massimo، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2000
Pages :
4
From page :
6527
To page :
6530
Abstract :
The reaction of cyclen 1 with chloral hydrate afforded exclusively 1,4,7-triformylcyclen 2 in high yield; the triprotected macrocycle was easily alkylated with various electrophiles in good to excellent yields. The alkaline removal of the formyl groups provided a selective entry into N-monosubstituted cyclen derivatives.
Journal title :
Tetrahedron Letters
Serial Year :
2000
Journal title :
Tetrahedron Letters
Record number :
1638529
Link To Document :
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