J. Org. Chem.
 1968
DOI: 10.1021/jo01274a002
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Organophosphorus chemistry. VIII. Reactions of triphenylphosphine with .alpha.-haloisobutyrophenones and with .alpha.-mesyloxyisobutyrophenone

Irving J. Borowitz1,
Kenneth C. Kirby2,
Paul E. Rusek3
et al.
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Cited by 4 publications
(1 citation statement)
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“…2-(l-Ethoxyethyl)-4-methylcyclohexanone (25): bp 96-97 °C (4 mm); IR (neat) 1720, 1110 cm-1; NMR (CC14) 0.95-1.21 (m,9 H), 1.61-2.44 (m, 8 ), 3.21-3.85 (m, 3 H). Anal.…”
Section: Resultsmentioning
confidence: 99%

Novel synthesis of .alpha.-methylene carbonyl compounds

Shono1,
Nishiguchi2,
Komamura3
et al. 1979
J. Am. Chem. Soc.
38
1
11
0
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“…2-(l-Ethoxyethyl)-4-methylcyclohexanone (25): bp 96-97 °C (4 mm); IR (neat) 1720, 1110 cm-1; NMR (CC14) 0.95-1.21 (m,9 H), 1.61-2.44 (m, 8 ), 3.21-3.85 (m, 3 H). Anal.…”
Section: Resultsmentioning
confidence: 99%

Novel synthesis of .alpha.-methylene carbonyl compounds

Shono1,
Nishiguchi2,
Komamura3
et al. 1979
J. Am. Chem. Soc.
38
1
11
0
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Use of moist silica gel for obtaining α-ethylenic carbonyl compounds from β-alkylthio or β-phenylthio allylic alcohols

Pellet
1
,
Huet
2
1988
Tetrahedron
13
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3
0
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A Superior Methacycline Synthesis by Phosphine or Phosphite Dehalogenation

Faubl
1
1976
Organic Preparations and Procedures International
1
0
0
0
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