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Philip L. Southwick

Carnegie Institution for Science

15

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The amino blocking reagent 1-isopropyl-3-ethoxy-4-nitro-2-oxo-3-pyrroline and the N-hydroxysuccinimide esters of N-(1-cyclohexyl- and 1-isopropyl-4-nitro-2-oxo-3-pyrrolin-3-yl)glycine. Reagents for the introduction of N-glycyl residues

1984 Journal of Organic Chemistry
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Phenylcinnamalones. 4. An oxidation reaction

1979 Journal of Organic Chemistry
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Phenylcinnamalones. III. Basic hydrolysis of phenylcinnamalone

1976 Journal of Organic Chemistry
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PHENYLCINNAMALONES PART 2, SOME DATA CONCERNING THE PREPARATIVE REACTION

1975 ChemInform
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Phenylcinnamalones. II. Data concerning the preparative reaction

1974 Journal of Organic Chemistry
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Nitro enol ether 4-nitro-1-cyclohexyl-3-ethoxy-2-oxo-3-pyrroline. Synthesis and use as a reagent for amino group protection

1974 Journal of Organic Chemistry
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Nitro enol, 3-hydroxy-4-nitro-5-phenyl-3-pyrrolin-2-one, and its reactive methyl ether

1969 Journal of Organic Chemistry
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1-Carbamoyl- and 1-aminomethyl-1,4-dihydropyrrolo[3,4-b]indole derivatives. Indole formation by fragmentation of strain-barrier stabilized 2-aminoindoline derivatives

1968 Journal of Organic Chemistry
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The synthesis of 6,7‐dihydro‐5H‐pyrrolo[3,4‐d]pyrimidines. II. 4‐Hydroxy, 4‐mercapto, 2‐amino‐4‐hydroxy and 2,4‐dihydroxy derivatives

1967 Journal of Heterocyclic Chemistry
- Tuvia Sheradsky
- Philip L. Southwick
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Enols in the Pyrrolidine Series. Reaction Site and Stereoselectivity in Reactions of Certain Aluminum and Boron Hydrides with α,β-Unsaturated Ketones and Their Enolic Reduction Products1a

1966 Journal of Organic Chemistry
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Citations (17)