1966
DOI: 10.1021/ja00963a023
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Tetrachlorocyclopropene, Tetrabromocyclopropene, and Some Fluorinated Cyclopropenes and Cyclopropanes1

Abstract: nmr spectrum of 4 shows a sharp singlet resonance at 76.2 ((-OCHsls); a doublet at 5.20 J = 1.2 cps (-CH(OR)z); and a doublet at 3.31, J -1.2 cps (C=C-H). The peak area ratios are 6:0.9:1.

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Cited by 82 publications
(24 citation statements)
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“…General comments: Tetrachlorocyclopropene [10] and the diarylcyclopropenones [11] were prepared according to literature. All experiments were carried out under dry argon using standard Schlenk or dry box techniques.…”
Section: Methodsmentioning
confidence: 99%
“…General comments: Tetrachlorocyclopropene [10] and the diarylcyclopropenones [11] were prepared according to literature. All experiments were carried out under dry argon using standard Schlenk or dry box techniques.…”
Section: Methodsmentioning
confidence: 99%
“…Analytical samples were by preparative GC. The physical and spectral data are reported elsewhere [15]. I , 6,7-Trichloro-7-fluoro-2,5-diphenylbicyclo[4.1.O]hept-3-ene (13).…”
Section: Discussionmentioning
confidence: 99%
“…281 This reaction was first discovered by Tobey and West in the 1960s 282283 and later investigated by Wright’s group for the synthesis of substituted cycloheptadienes. 284–290 After the Diels-Alder cycloaddition, a sequence of rearrangement, hydrolysis in the presence of silver salts, addition of isopropyl zinc cuprate to enone and reduction by samarium diiodide yielded the tropolone natural product.…”
Section: Synthesis Of Naturally Occurring Tropones and Tropolonesmentioning
confidence: 99%