Synthesis of polymers carrying adamantyl substituents in side chain | Polymer Journal
Catalysts Containing the Adamantane Scaffold - Agnew‐Francis - 2016 - Advanced Synthesis & Catalysis - Wiley Online Library
1-Adamantyl methyl ketone 99 1660-04-4
![1-[[(3-Hydroxy-1-adamantyl)amino]acetyl]-2-cyano-(S)-pyrrolidine: A Potent, Selective, and Orally Bioavailable Dipeptidyl Peptidase IV Inhibitor with Antihyperglycemic Properties | Journal of Medicinal Chemistry](https://pubs.acs.org/cms/10.1021/jm030091l/asset/images/large/jm030091ln00001.jpeg "1-[[(3-Hydroxy-1-adamantyl)amino]acetyl]-2-cyano-(S)-pyrrolidine: A Potent, Selective, and Orally Bioavailable Dipeptidyl Peptidase IV Inhibitor with Antihyperglycemic Properties | Journal of Medicinal Chemistry")
1-[[(3-Hydroxy-1-adamantyl)amino]acetyl]-2-cyano-(S)-pyrrolidine: A Potent, Selective, and Orally Bioavailable Dipeptidyl Peptidase IV Inhibitor with Antihyperglycemic Properties | Journal of Medicinal Chemistry
1-Adamantyl methyl ketone, 99%, Thermo Scientific Chemicals
1-Acetyladamantane 1660-04-4 | TCI AMERICA
1-Adamantyl methyl ketone 99 1660-04-4
Poly(ether ketone)
Ketone 1 | Sigma-Aldrich
Tri(1-adamantyl)phosphine: Expanding the Boundary of Electron-Releasing Character Available to Organophosphorus Compounds | Journal of the American Chemical Society
Synthesis and Radical Polymerization of Adamantyl Methacrylate Monomers Having Hemiacetal Moieties | Macromolecules
PDF) Oxidative functionalization of adamantanes (review)
1-Adamantyl methyl ketone 99 1660-04-4
1-Adamantyl methyl ketone | C12H18O - PubChem
FA03711 | 1660-04-4 | 1-Adamantyl methyl ketone
1-Adamantyl methyl ketone, 99%, Thermo Scientific Chemicals | Fisher Scientific
1-Adamantyl methyl ketone | C12H18O - PubChem
Adamantane - Wikipedia
FA07663 | 4942-47-6 | 1-Adamantane acetic acid | Biosynth
1-Adamantyl methyl ketone (CAS 1660-04-4) - Chemical & Physical Properties by Cheméo
The many faces of the adamantyl group in drug design - ScienceDirect
1-Adamantyl methyl ketone (CAS 1660-04-4) - Chemical & Physical Properties by Cheméo
1-Adamantyl methyl ketone(1660-04-4) 1H NMR spectrum
Tautomerization in Naphthalenediimines: A Keto-Enamine Schiff Base Macrocycle | Organic Letters
