154367-62-1Relevant academic research and scientific papers
Chemistry of pyrrolizinones. Part 1. Reactions of pyrrolizin-3-ones with electrophiles: Synthesis of 3,8-didehydroheliotridin-5-one
McNab, Hamish,Thornley, Craig
, p. 3584 - 3591 (2007/10/03)
The reaction of pyrrolizin-3-one 1 with dry hydrogen chloride gives the 1-chloro-1,2-dihydro derivative 8 (93%) by electrophilic addition. The halogen of 8 is readily displaced by O-nucleophiles to give 6, 9 or 10 in 87-100% yield, and this strategy has been employed in a short synthesis of the necine base didehydroheliotridin-5-one 4. Pyrrolizinone 1 can be brominated by N-bromosuccinimide in the presence of nucleophiles to give 20 or 21, or under free radical conditions to give the 2-bromopyrrolizinone 22 (55%). Vilsmeier formylation of 1 gave a variety of products including the 5-formylpyrrolizinone 26 (16%), but azo-coupling could only be observed under basic conditions to give the coupled propenoate 31 (46%) via the anion of the ring-opened species 30. The Royal Society of Chemistry 2000.
New Chemistry of Pyrrolizin-3-one: a Concise Route to 3,8-Didehydroheliotridin-5-one
McNab, Hamish,Thornley, Craig
, p. 1570 - 1571 (2007/10/02)
1-Substituted 1,2-dihydropyrrolizin-3-ones can be obtained from pyrrolizin-3-one 2 by conjugate nucleophilic addition or electrophilic addition reactions; the 1-chloro compound 9 obtained by the latter method is used as a key intermediate in a six-step synthesis of the title compound 3 from 4-acetoxymethylpyridine-N-oxide.
