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- W2075736718 abstract "Benzothiete 1 generates by thermal ring opening an 8π electron system 2 which undergoes [8π + 2π] cycloaddition reactions with the oxime systems 3a-g. In accordance with the FMO theory the 1,3-thiazine derivatives 4a-g are formed in a regiospecific and 4f additionally in a stereospecific manner. The O-acylated adducts 4h-j enter the same cycloaddition; however, an elimination reaction 4 ← 5, 6 can provoke the addition of a second benzothiete, yielding the tetracyclic compounds 7j, and 8i,j." @default.
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- W2075736718 date "1991-06-01" @default.
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- W2075736718 title "Cycloaddition von benzothiet an oxime, oximether und oximester" @default.
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- W2075736718 doi "https://doi.org/10.1002/jhet.5570280402" @default.
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