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Dive into the research topics where John F. Kelly is active.

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Featured researches published by John F. Kelly.


Journal of Organic Chemistry | 1968

The reaction of chlorosulfonyl isocyanates with allenes and olefins

Emil J. Moriconi; John F. Kelly


Journal of Organic Chemistry | 1971

Unsaturated heterocyclic systems. LXXVII. 1-Aza-2,4,6-cyclooctatriene-7-azabicyclo[4,2,] octadiene valence tautomeric equilibrium. Substituent effects and an attempted synthesis of azetes (azacyclobutadienes)

Leo A. Paquette; Tsuyoshi Kakihana; John F. Kelly


Journal of the American Chemical Society | 1971

Stretched benzene. Kinetic analysis of possible pseudoaromaticity resulting from (2 + 2 + 1 + 1) partitioning of a neutral six-orbital six-electron system

Leo A. Paquette; Michael R. Short; John F. Kelly


Journal of the American Chemical Society | 1966

β-Lactams Containing an Exocyclic Double Bond1

Emil J. Moriconi; John F. Kelly


Journal of Organic Chemistry | 1971

Unsaturated heterocyclic systems. LXXVIII. Neighboring group participation by sulfonamide nitrogen. 7-Azabicyclo [4.2.] oct-3-ene to 6-azabicyclo[3.2.1] oct-2-ene rearrangement

Leo A. Paquette; John F. Kelly


Tetrahedron Letters | 1970

The reaction of acetylenes with chlorosulfonyl isocyanate

Emil J. Moriconi; John G. White; Richard W. Franck; JoAnn Jansing; John F. Kelly; Ramon A. Salomone; Yasuo. Shimakawa


Journal of Organic Chemistry | 1968

Olefinic intermediates in the reaction of 1,1-dimethyl-1,1,2-trimethyl and 1,1,2,2-tetramethylcyclopropanes with chlorosulfonyl isocyanate

Emil J. Moriconi; John F. Kelly; Ramon A. Salomone


Tetrahedron Letters | 1968

The stereospecific cycloaddition of chlorosulfonyl isocyanate to cis- and trans-β-methylstyrene and cis- and trans-3-hexene

Emil J. Moriconi; John F. Kelly


Tetrahedron Letters | 1969

1,6-Cycloaddition of chlorosulfonyl isocyanate to cycloheptatriene

Emil J. Moriconi; Charles F. Hummel; John F. Kelly


ChemInform | 1972

′GESPANNTES BENZOL′, KINETISCHE ANALYSE MOEGLICHER PSEUDOAROMATIZITAET ALS FOLGE EINER (2+2+1+1)-VERTEILUNG EINES NEUTRALEN SECHS-ORBITAL-SECHS-ELEKTRONEN-SYST.

Leo A. Paquette; Michael R. Short; John F. Kelly

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