1,177–1,200 of 3,374
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Cupferron
Org. Synth. Coll. Vol. 1, p. 177; Vol. 4, p. 19 · Marvel
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Cuprous ion-catalyzed oxidative cleavage of aromatic o-diamines by oxygen: (Z,Z)-2,4-hexadienedinitrile
Org. Synth. Coll. Vol. 6, p. 662; Vol. 57, p. 33 · Tsuji and Takayanagi
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Cyanic acid esters from phenols: phenyl cyanate
Org. Synth. Coll. Vol. 7, p. 435; Vol. 61, p. 35 · Martin and Bauer
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Cyanide-catalyzed conjugate addition of aryl aldehydes: 4-oxo-4-(3-pyridyl)butyronitrileAddition
Org. Synth. Coll. Vol. 6, p. 866; Vol. 59, p. 53 · Stetter et al.
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1-Cyano-3-phenylurea
Org. Synth. Coll. Vol. 4, p. 213; Vol. 36, p. 8 · Kurzer and Powell
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3-Cyano-6-methyl-2(1)-pyridone
Org. Synth. Coll. Vol. 4, p. 210; Vol. 32, p. 32 · Mariella
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2-Cyano-6-methylpyridine
Org. Synth. Coll. Vol. 5, p. 269; Vol. 42, p. 30 · Feely et al.
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α-Cyano-β-phenylacrylic acid
Org. Synth. Coll. Vol. 1, p. 181; Vol. 7, p. 20 · Lapworth and Baker
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Cyanoacetamide
Org. Synth. Coll. Vol. 1, p. 179; Vol. 9, p. 36 · Corson et al.
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1-Cyanobenzocyclobutene
Org. Synth. Coll. Vol. 5, p. 263; Vol. 48, p. 55 · Skorcz and Kaminski
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N-2-Cyanoethylaniline
Org. Synth. Coll. Vol. 4, p. 205; Vol. 36, p. 6 · Cymerman-Craig and Moyle
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Cyanogen bromide
Org. Synth. Coll. Vol. 2, p. 150; Vol. 11, p. 30 · Hartman and Dreger
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Cyanogen iodide
Org. Synth. Coll. Vol. 4, p. 207; Vol. 32, p. 29 · Bak and Hillebert
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7-Cyanoheptanal
Org. Synth. Coll. Vol. 5, p. 266; Vol. 49, p. 27 · Ohno et al.
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9-Cyanophenanthrene
Org. Synth. Coll. Vol. 3, p. 212; Vol. 28, p. 34 · Callen et al.
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Cyclic ketones from 1,3-dithiane: cyclobutanone
Org. Synth. Coll. Vol. 6, p. 316; Vol. 51, p. 76 · Seebach and Beck
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[4+3] Cycloaddition in water. Synthesis of 2,4-endo,endo-dimethyl-8-oxabicyclo[3.2.1]oct-6-en-3-oneCycloaddition
Org. Synth. Vol. 79, p. 251 · Lautens and Bouchain
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[4+2] Cycloaddition of 1-dimethylamino-3-tert-butyldimethylsiloxy-1,3-butadiene with methyl acrylate: 4-hydroxymethyl-2-cyclohexen-1-oneCycloaddition
Org. Synth. Vol. 78, p. 160 · Kozmin et al.
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[4 + 3] Cycloaddition of aminoallyl cations with 1,3-dienes: 11-oxatricyclo[4.3.1.12,5]undec-3-en-10-oneCycloaddition
Org. Synth. Vol. 78, p. 212 · Oh et al.
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Cyclobutadiene in synthesis: endo-tricyclo[4.4.0.02,5]deca-3,8-diene-7,10-dione
Org. Synth. Coll. Vol. 6, p. 1002; Vol. 55, p. 43 · Brener et al.
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Cyclobutadieneiron tricarbonyl
Org. Synth. Coll. Vol. 6, p. 310; Vol. 50, p. 21 · Pettit and Henery
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1,1-Cyclobutanedicarboxylic acid and cyclobutanecarboxylic acid
Org. Synth. Coll. Vol. 3, p. 213; Vol. 23, p. 16 · Heisig and Stodola
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1,2-Cyclobutanedione
Org. Synth. Coll. Vol. 7, p. 112; Vol. 60, p. 18 · Denis et al.
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Cyclobutanone
Org. Synth. Coll. Vol. 7, p. 114; Vol. 60, p. 20 · Krumpolc and Rocek