Chemical research careers are more diverse than they might first appear, as there are many different reasons to conduct research and many possible environments. 459-56-3, Name is (4-Fluorophenyl)methanol, SMILES is OCC1=CC=C(F)C=C1, in an article , author is Schnurch, Michael, once mentioned of 459-56-3, Synthetic Route of 459-56-3.
Recent progress in the field of transition-metal-catalyzed cross-coupling reactions on various azole systems is summarized. Most important C-C- and C-X-bond formation methodologies (Negishi, Suzuki-Miyaura, Stille, Kumada-Corriu-Tamao, Hiyama, Sonogashira, Heck, C-H activation) are reviewed and discussed for the imidazole, oxazole, thiazole, pyrazole, isoxazole, and isothiazole system, as well as for azoles with more than two heteroatoms. This review covers the literature that appeared in the past ten years up to the end of 2005 with corresponding azoles used either as metal organyl or halide (including triflates and some other less frequently applied leaving groups); literature describing azole structures only as ligands was not included. ((c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006).
Synthetic Route of 459-56-3, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect. I hope my blog about 459-56-3 is helpful to your research.
Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com