Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000084.xml
Synthesis 2012(7): 1090-1094
DOI: 10.1055/s-0031-1289719
DOI: 10.1055/s-0031-1289719
PAPER
© Georg Thieme Verlag
Stuttgart ˙ New York
Extending Triazolyl-Based Release under Mildly Acidic Conditions To Give Aniline Derivatives
Further Information
Received
8 December 2011
Publication Date:
24 February 2012 (online)
Publication History
Publication Date:
24 February 2012 (online)
Abstract
Triazolyl derivatives of anilines were prepared and evaluated as releasing systems at mildly acidic pH values. Two triazolyl derivatives showed convenient pH sensitivity, being stable at pH 7.3 and rapidly hydrolyzed at pH values below 5. A generalized mechanism is proposed from additional theoretical investigations.
Key words
hydrolysis - alkynes - azides - cycloaddition - amines - protonation
- 1
White S.Szewczyk JW.Turner JM.Baird EE.Dervan PB. Nature 1998, 391: 468 - 2
Maeda H. Bioconjugate Chem. 2010, 21: 797 - 3
Zhang H.Wang G.Yang H. Expert Opin. Drug Delivery 2011, 8: 171 -
4a
Patel VF.Hardin JN.Mastro JM.Law KL.Zimmermann JL.Ehlhardt WJ.Woodland JM.Starling JJ. Bioconjugate Chem. 1996, 7: 497 -
4b
Fréchet JMJ.Gillies ER.Goodwin AP. Bioconjugate Chem. 2004, 15: 1254 - 5
Delatouche R.Mondon M.Gil A.Frapper G.Bachmann C.Bertrand P. Tetrahedron 2011, 67: 401 - 6
Mondon M.Delatouche R.Bachmann C.Frapper G.Len C.Bertrand P. Eur. J. Org. Chem. 2011, 2111 -
7a
Huisgen R. Angew. Chem., Int. Ed. Engl. 1963, 2: 565 -
7b
Huisgen R. Angew. Chem., Int. Ed. Engl. 1963, 2: 633 -
7c
Kolb HC.Finn MG.Sharpless KB. Angew. Chem. Int. Ed. 2001, 40: 2004 -
7d
Bertrand P.Gesson J.-P.
J. Org. Chem. 2007, 72: 3596 - 8
Gooding OW.Beard CC.Jackson DY.Wren DL.Cooper GF. J. Org. Chem. 1991, 56: 1083 - 9
Streidl N.Antipova A.Mayr H. J. Org. Chem. 2009, 74: 7328 - 10
Bertrand P. Eur. J. Med. Chem. 2010, 45: 2095 - 11
Ringdahl B. Tetrahedron 1979, 35: 2413