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Butadiene monoxide is used as key starting material for the synthesis of (-)-bulgecinine and (+)-broussonetine G.
Reaction with allyl bromide, mediated by In metal, affords diallylmethanol: Tetrahedron Lett., 44, 2911 (2003):
Li, G.; Feng, X.; Du, H. Palladium-catalyzed asymmetric allylic amination of racemic butadiene monoxide with isatin derivatives. Org. Biomol. Chem. 2015, 13 (20), 5826-5830.
Mao, W.; He, H. H.; Gu, J. Q.; Chen, W.; Wu, K.; Tok, E. S.; Xu, G. Q. Preservation of epoxy groups on surfaces in the covalent attachment of butadiene monoxide on Si(111)-(7×7): the effect of a vinyl substituent. Chem. Commun. 2015, 51 (75), 14195-14198.
Gefahrenhinweise (EU): H225-H341
Highly flammable liquid and vapour. Suspected of causing genetic defects.
Do not breathe dust/fume/gas/mist/vapours/spray. Obtain special instructions before use. Wear protective gloves and eye/face protection. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.