Synthesis of anatoxin a via intramolecular Mannich reaction was written by Suh, Young-Ger;Choi, Young Gi;Ryu, Jae Sang;Cho, Youn-Sang. And the article was included in Soul Taehakkyo Yakhak Nonmunjip in 1995.Recommanded Product: 2-(3-Bromopropyl)-1,3-dioxolane This article mentions the following:
Total synthesis of anatoxin a which consists of unusual azabicyclo[4.2.1]nonane skeleton has been investigated. As a key part of this synthesis, intramol. Mannich reaction for the construction of azabicyclo[4.2.1]nonane system has been employed. In the experiment, the researchers used many compounds, for example, 2-(3-Bromopropyl)-1,3-dioxolane (cas: 62563-07-9Recommanded Product: 2-(3-Bromopropyl)-1,3-dioxolane).
2-(3-Bromopropyl)-1,3-dioxolane (cas: 62563-07-9) belongs to dioxole derivatives. Dioxoles, particularly fluorinated dioxoles, are used as co-monomers to make polymers that find use in forming protective coatings for chemical resistance. 1,3-Benzodioxole can be synthesized from catechol with disubstituted halomethanes.Recommanded Product: 2-(3-Bromopropyl)-1,3-dioxolane
Referemce:
1,3-Benzodioxole – Wikipedia,
Dioxole | C3H4O2 – PubChem