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adamantanecarboxylic acid

Known as: 1-adamantanecarboxylic acid 
National Institutes of Health

Papers overview

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2011
2011
The Koch–Haaf reaction of adamantanols was successfully carried out in a microflow system at room temperature. By combining an… 
2008
2008
We report temperature-dependent ultrasonic velocimetric and densimetric data on changes in volume, expansibility, and adiabatic… 
2005
2005
Partially ordered FePtAu nanoparticles with size around 8 nm were prepared by the simultaneous decomposition of iron… 
Highly Cited
2003
Highly Cited
2003
[structure: see text] Allylic substitution of allyl alcohols in water as a suspension medium has been realized using a… 
2002
2002
A 1:1 mixture of a tris(Zn(II)-cyclen) (1: [Zn(3)L(1)], L(1)=1,3,5-tris(1,4,7,10-tetraazacyclododecan-1-ylmethyl)benzene) and… 
1991
1991
Abstract— Acylation of the N‐terminus of [d‐Arg0, Hyp3, Thi5.8, d‐Phe7] bradykinin with 1‐adamantanecarboxylic acid results in an… 
Review
1987
Review
1987
The discovery of 1964 of the antiviral activity (AA) of l-aminoadamantane and a number of its derivatives [149] led to intensive… 
1987
1987
1 Adamantane derivatives were found to increase insulin release in vitro. Mouse islets were used to study the mechanisms and…