SYNTHESIS, CHEMICAL-REACTIVITY, AND CYTOTOXICITY OF 2-BIS(ALKOXYCARBONYL)METHYLIDEN-1-AZABICYCLO[3.1.0]HEXANE SYSTEMS RELATED TO ANTITUMOR ANTIBIOTIC CARZINOPHILIN-A
被引:22
作者:
HASHIMOTO, M
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SAGAMI CHEM RES CTR, SAGAMIHARA, KANAGAWA 229, JAPANSAGAMI CHEM RES CTR, SAGAMIHARA, KANAGAWA 229, JAPAN
HASHIMOTO, M
[1
]
YAMADA, K
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SAGAMI CHEM RES CTR, SAGAMIHARA, KANAGAWA 229, JAPANSAGAMI CHEM RES CTR, SAGAMIHARA, KANAGAWA 229, JAPAN
YAMADA, K
[1
]
TERASHIMA, S
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SAGAMI CHEM RES CTR, SAGAMIHARA, KANAGAWA 229, JAPANSAGAMI CHEM RES CTR, SAGAMIHARA, KANAGAWA 229, JAPAN
TERASHIMA, S
[1
]
机构:
[1] SAGAMI CHEM RES CTR, SAGAMIHARA, KANAGAWA 229, JAPAN
Enantiomeric pairs of the title compounds were synthesized starting from (S)- and (R)-pyroglutamic acid. They were found to be susceptible to nucleophilic ring opening of aziridine moieties and to exhibit weak in vitro cytotoxicity.