Grandma made a deal with Cri-kee. She won't blindly cross the street with him if Cri-kee can find at least three references that prove how dangerous her actions are (or related to the reaction). Look below to see the references he found!

Other Papers that cited Fukuzawa, S.; Tsuchimoto T.; Hotaka, T.; Hiyama, T. Synlett, 1995, 1077-1078.

Oishi, T.; Hasegwa, F.; Torikai, K.; Konoki, K.; Matsumori, N.; Murata, M. Org. Lett., 2008, 10, 3599-3602.

This paper cited Fukuzawa’s paper because one of the synthesis steps involves the regioselective opening of the seven-membered ring acetal using TMSCN and Sc(OTf)3. Fukuzawa’s paper discussed the use of Sc(OTf)3 as a catalyst in acetal reactions.

 

Ishihara, K.; Karumi, Y.; Kubota, M.; Yamamoto, H. Synlett. 1996, 9, 839-841.

The paper cited Fukuzawa’s paper because they use Sc(OTf)3 as a Lewis acid catalyst in acetal reactions, which is similar to Fukuzawa’s use of Sc(OTf)3. They even found that the Sc(OTf)3 catalyst was more efficient than p-TsOH. 

 

Mitchell, L.; Gonzalez-Santiago, B.; Mowat, J. P. S.; Williamson, P.; Acerbi, N.; Clarke, M. L.; Wright, P. A. Catalysis Science & Technology. 2013, 3, 606.

This paper cited Fukuzawa’s paper due to their use of scandium trimestate MIL-100(sc) as a strong lewis acid. Fukuzawa’s paper used Sc(OTf)3 in a similar way.