1596803-18-7Relevant articles and documents
A Route to Cyclooct-2-ynol and Its Functionalization by Mitsunobu Chemistry
Hagendorn, Tobias,Br?se, Stefan
, p. 1280 - 1286 (2015/10/05)
A new silver-free synthesis for cyclooctynol is introduced. The obtained alcohol was further functionalized by a Mitsunobu reaction to give an assortment of imide and phenol derivatives. It was also possible to further functionalize the cyclooctyne by treatment with a fluorescein dye. As an interesting application, we used a cyclooctyne-maleimide conjugate as an azide-thiol crosslinker. A new synthesis for cyclooct-2-ynol is presented that does not employ silver salts. The obtained alcohol was further functionalized by Mitsunobu chemistry to afford new cyclooctynes.