Protonated diacetone alcohol and protonated 4- hydroxy-3-methyl-2-butanone undergo vinylation and colli- sion-induced dehydration as the only primary reactions, the product of the former reaction consisting of up to 40% of the total product ion distribution.
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Applications
Protonated diacetone alcohol and protonated 4- hydroxy-3-methyl-2-butanone undergo “vinylation” and colli- sion-induced dehydration as the only primary reactions, the product of the former reaction consisting of up to 40% of the total product ion distribution.
Notes
Hygroscopic. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents.
RUO – Research Use Only
General References:
- Masahiro Hirama,; Kenshu Fujiwara,; Kuniyoshi Shigematu,; Yoshimasa Fukazawa.The 10-membered ring analogs of neocarzinostatin chromophore: design, synthesis and mode of decomposition. J. Am. Chem. Soc. 1989, 111 (11), 4120-4122.
- Xiaoyu Liu,; Harvey E. Jeffries,; Kenneth G. Sexton. Atmospheric Photochemical Degradation of 1,4-Unsaturated Dicarbonyls. Environ. Sci. Technol. 1999, 33 (23),4212-4220.