Yamada Kohei, Hayakawa Naoko, Fujita Hikaru, Kitamura Masanori, Kunishima Munetaka
Faculty of Pharmaceutical Sciences, Institute of Medical, Pharmaceutical, and Health Sciences, Kanazawa University.
Chem Pharm Bull (Tokyo). 2017;65(1):112-115. doi: 10.1248/cpb.c16-00744.
Acid-catalyzed allylating reagent 2,4,6-tris(allyloxy)-1,3,5-triazine (TriAT-allyl) and its substituted derivatives have been developed. The reaction of acid-, and alkali-labile alcohols with these reagents in the presence of a catalytic amount of trifluoromethanesulfonic acid (TfOH) afforded the corresponding allyl ethers in good yields. Reactions using these reagents with an unsymmetrically-substituted regioisometric allyl group suggested that a single isometric allylic cation species would be involved.
已开发出酸催化烯丙基化试剂2,4,6-三(烯丙氧基)-1,3,5-三嗪(三烯丙基三嗪,TriAT-烯丙基)及其取代衍生物。在催化量的三氟甲磺酸(TfOH)存在下,酸不稳定和碱不稳定的醇与这些试剂反应,以良好的产率得到相应的烯丙基醚。使用这些试剂与不对称取代的区域异构烯丙基进行的反应表明,将涉及单一的区域异构烯丙基阳离子物种。