118625-56-2Relevant academic research and scientific papers
FUNCTIONALIZED SILOXY-ANCHORED MONOLAYERS WITH EXPOSED AMINO, AZIDO, BROMO, OR CYANO GROUPS
Balachander, Natarajan,Sukenik, Chaim N.
, p. 5593 - 5594 (1988)
The creation of new, uniformly functionalized, surfaces has been achieved with monolayers bearing NH2, N3, Br, or CN functional groups.
An Efficient Synthesis of 3-Alkylpyridine Alkaloids Enables Their Biological Evaluation
Kaplan, Anna R.,Schrank, Cassandra L.,Wuest, William M.
, p. 2487 - 2490 (2021)
3-Alkylpyridine alkaloids (3-APAs) isolated from the arctic sponge Haliclona viscosa are a promising group of bioactive marine alkaloids. However, due to limited bioavailability, investigations of their bioactivity have been hampered. Additionally, synthesis of a common intermediate requires the use of protecting groups and harsh conditions. In this work, we developed a simple and concise two-step route to nine different natural and synthetic haliclocyclins. These compounds displayed modest antibiotic activity against several Gram-positive bacterial strains.
Synthesis of model compounds for the formation of self-assembled monolayers on a silicon surface
Effenberger,Heid
, p. 1126 - 1130 (2007/10/02)
The synthesis of terminally functionalized alkanes, which represent potential compounds for formation of self-assembled monolayers, is reported. The alkanes described are substituted at one end with a trichloro- or trialkoxysilyl group suitable for linkage to a hydroxylated silicon surface and at the other end with a vinyl or amino group for further functionalization.
