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• W3007825071 endingPage "1934578X1989668" @default.
• W3007825071 startingPage "1934578X1989668" @default.
• W3007825071 abstract "Reaction of d-camphor p-toluenesulfonylhydrazone with t-butoxide and elemental selenium in dimethylformamide at an elevated temperature afforded a stable compound having a unique 1,6,6αλ 4 -triselenapentalene ring and 4 H-selenopyran-4-selones along with dialkenyl diselenide, dibornylenes, and 1,2,5-triselenepin, and the structural confirmation of these products were carried out by X-ray crystallographic analysis. The sterically crowded 1,6,6aλ 4 -triselenapentalene ring fused with two bornane sleketons was stable enough under aerobic exposure and was inactive toward sodium borohydride reduction but was converted into 1,2-diselenole derivative through m-chloroperbenzoic acid oxidation." @default.
• W3007825071 created "2020-03-06" @default.
• W3007825071 creator A5033802964 @default.
• W3007825071 creator A5046838381 @default.
• W3007825071 creator A5062883841 @default.
• W3007825071 date "2020-02-01" @default.
• W3007825071 modified "2023-09-26" @default.
• W3007825071 title "Formation of a Sterically Crowded 1,6,6αλ⁴-Triselenapentalene and 4<i>H</i>-Selenopyran-4-selones Fused with Two Bornane Skeletons Through the Reaction of <i>d</i>-Camphor <i>p</i>-Toluenesulfonylhydrazone With a Base and Elemental Selenium" @default.
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• W3007825071 doi "https://doi.org/10.1177/1934578x19896686" @default.
• W3007825071 hasPublicationYear "2020" @default.
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