198,617 research outputs found
on the thermal decomposition of diazirines
No full textPT: J; CR: BIGOT B, 1978, J AM CHEM SOC, V100, P6576 BRADLEY GF, 1977, J CHEM SOC P2, P1214 BRUNNER J, 1980, J BIOL CHEM, V255, P3313 DIDERICH G, 1972, HELV CHIM ACTA, V55, P2103 FLEMING I, 1980, FRONTIER ORBITALS OR GRILLER D, 1982, J AM CHEM SOC, V104, P5549 JENNINGS BM, 1976, J AM CHEM SOC, V98, P6416 LAHMANI F, 1976, J PHYS CHEM-US, V80, P2623 LANGANIS ED, 1983, J AM CHEM SOC, V105, P7457 LIU MTH, 1972, J PHYS CHEM-US, V76, P797 LIU MTH, 1973, CAN J CHEM, V51, P2393 LIU MTH, 1974, J CHEM SOC P2, P937 LIU MTH, 1977, CAN J CHEM, V55, P3596 LIU MTH, 1982, CHEM SOC REV, V11, P127 MOORE CB, 1964, J CHEM PHYS, V41, P3504 SCHMITZ E, 1965, CHEM BER, V98, P2509 SCHMITZ E, 1967, CHEM BER, V100, P2093 SCHMITZ E, 1971, 23RD INT C PUR ALL C, V2, P283 SHEPARD RA, 1967, J ORG CHEM, V32, P3197 SHILOV AE, 1968, TETRAHEDRON LETT, P4177 SMITH NP, 1979, J CHEM SOC P2, P213 SMITH RAG, 1975, J CHEM SOC P2, P686 SNYDER JP, 1972, TETRAHEDRON LETT, P4347 TAYLOR EC, 1979, CHEM REV, V79, P181 TURRO NJ, 1980, J AM CHEM SOC, V102, P7576 TURRO NJ, 1982, J AM CHEM SOC, V104, P1754 VOIGT E, 1975, CHEM BER, V108, P3326 ZOLLINGER H, 1978, ANGEW CHEM INT EDIT, V17, P141; NR: 28; TC: 8; J9: J CHEM SOC PERKIN TRANS 2; PG: 4; GA: A2035Source type: Electronic(1
Substituent and temperature effects on the reactions of benzylchlorocarbene with alcohol
No full textPT: J; CR: DOLBY LJ, 1966, J ORG CHEM, V31, P110 FRENKING G, 1984, TETRAHEDRON, V40, P2123 GRAHAM WH, 1965, J AM CHEM SOC, V87, P4396 GRILLER D, UNPUB GRILLER D, 1982, J AM CHEM SOC, V104, P5549 GRILLER D, 1984, J AM CHEM SOC, V106, P198 KIRMSE W, 1971, CARBENE CHEM KIRMSE W, 1981, J AM CHEM SOC, V103, P5935 LIU MTH, 1984, J CHEM SOC CHEM COMM, P1062 LIU MTH, 1985, J CHEM SOC CHEM COMM, P982 MARCH J, 1985, ADV ORG CHEM, P244 MOSS RA, 1975, CARBENES, V1 MOSS RA, 1975, CARBENES, V2 MOSS RA, 1983, TETRAHEDRON LETT, V24, P685 MUROV SL, 1973, HDB PHOTOCHEMISTRY, P147 PLATZ MS, 1982, J AM CHEM SOC, V104, P6494 SCHLOSSER M, 1967, CHEM BER, V100, P3901 SCHMID GH, 1978, J ORG CHEM, V43, P777 SENTHILNATHAN VP, 1980, J AM CHEM SOC, V102, P7637 TANAKA R, 1971, TETRAHEDRON, V27, P2651 TOMIOKA H, 1983, J AM CHEM SOC, V105, P5053 TOMIOKA H, 1984, J AM CHEM SOC, V106, P454 TOMIOKA H, 1984, J CHEM SOC CHEM COMM, P476 TOMIOKA H, 1984, TETRAHEDRON LETT, V25, P4413 WARNER P, 1984, J ORG CHEM, V49, P3666 WARNER PM, 1984, J AM CHEM SOC, V106, P5366 WRIGHT BB, 1984, J AM CHEM SOC, V106, P4175; NR: 27; TC: 9; J9: J CHEM SOC PERKIN TRANS 2; PG: 8; GA: D7012Source type: Electronic(1
The thermal decomposition of diazirines: 3-(3-methyldiazirin-3-yl)propan-1-ol and 3-(3-methyldiazirin-3-yl)propanoic acid
No full textPT: J; CR: BIGOT B, 1978, J AM CHEM SOC, V100, P6575 BRIDGE MR, 1969, J CHEM SOC A, P91 CHURCH RFR, 1970, J ORG CHEM, V35, P2465 CLOSS GL, 1965, J AM CHEM SOC, V87, P4270 EFFIO A, 1980, J AM CHEM SOC, V102, P1734 FIGUERA JM, 1976, AN QUIM, V72, P737 FIGUERA JM, 1978, J CHEM SOC F1, V74, P809 FIGUERA JM, 1979, J PHOTOCHEM, V10, P473 FREY HM, 1963, J CHEM SOC, P3514 FREY HM, 1964, J CHEM SOC, P4700 FREY HM, 1965, J CHEM SOC, P1700 FREY HM, 1965, J CHEM SOC, P3101 FREY HM, 1966, J CHEM SOC A, P968 FREY HM, 1977, J CHEM SOC F1, V73, P2010 FREY HM, 1979, J CHEM SOC A, P1916 GANZER GA, 1986, J AM CHEM SOC, V108, P1517 GRILLER D, 1982, J AM CHEM SOC, V104, P5549 LAL D, 1974, J AM CHEM SOC, V96, P6355 LIU MTH, 1972, INT J CHEM KINET, V4, P229 LIU MTH, 1972, J PHYS CHEM-US, V76, P797 LIU MTH, 1973, CAN J CHEM, V51, P2393 LIU MTH, 1974, J CHEM SOC P2, P937 LIU MTH, 1977, CAN J CHEM, V55, P3596 LIU MTH, 1982, CHEM SOC REV, V11, P127 LIU MTH, 1984, J CHEM SOC CHEM COMM, P1062 LIU MTH, 1984, TETRAHEDRON, V40, P887 LIU MTH, 1985, J CHEM SOC CHEM COMM, P982 LIU MTH, 1986, J CHEM SOC PERK T 2, P211 LIU MTH, 1987, CHEM DIAZIRINES, V1, P111 MANSOOR AM, 1966, TETRAHEDRON LETT, P1753 MANSOOR M, 1967, THESIS U SOUTHAMPTON MOSS RA, 1984, TETRAHEDRON LETT, V25, P1023 NEUVARAND EW, 1967, J PHYS CHEM-US, V71, P1229 SCHMID P, 1979, INT J CHEM KINET, V11, P333 SHERIDAN RS, 1984, J AM CHEM SOC, V106, P436 SKELL PS, 1972, TETRAHEDRON, V28, P3571 SMITH NP, 1979, J CHEM SOC P2, P213 SMITH RAG, 1975, J CHEM SOC P2, P686 VOIGT E, 1975, CHEM BER, V108, P3326; NR: 39; TC: 8; J9: J CHEM SOC PERKIN TRANS 2; PG: 7; GA: DD960Source type: Electronic(1
Thermodynamic Nitration Rates of Aromatic Compounds. Part 4. Temperature Dependence in Sulfuric Acid of Nitration Rates , HNO3--->NO2+ Equilibria and Acidic Properties of the Solvent
No full textJ.CHEM. SOC. PERKIN TRANS.
Not quite the last word on the Perkin reaction
No full textMicrowave irradiation does not accelerate the rate of the Perkin reaction carried out under normal atmosphericpressure. Water is an essential yet catalytic reactant for the Perkin reaction to occur. Containment of the Perkin reaction in a sealed vessel improves the yield. Two pressure increases are observed during a 4 h reaction time. An induction period is seen in the Perkin reaction when sodium acetate is used as a base. A re-appraisal of the reaction mechanism is proposed on the basis of these observations. The use of PFA reaction vessels enables the Perkin reaction to occur under aqueousconditions for around 80 reactions/vessel
Linear Oligopeptides. Part 352. Synthesis, Characterization and Solution Conformational Analysis of C(alfa)-methyl-homo-phenylalanine Containing Peptides
No full textJ. CHEM. SOC. , PERKIN TRANS.
Not quite the last word on the Perkin reaction
No full textMicrowave irradiation does not accelerate the rate of the Perkin reaction carried out under normal atmospheric pressure. Water is an essential yet catalytic reactant for the Perkin reaction to occur. Containment of the Perkin reaction in a sealed vessel improves the yield. Two pressure increases are observed during a 4 h reaction time. An induction period is seen in the Perkin reaction when sodium acetate is used as a base. A re-appraisal of the reaction mechanism is proposed on the basis of these observations. The use of PFA® reaction vessels enables the Perkin reaction to occur under aqueous conditions for around 80 reactions/vessel
Perfluoroalkanesulfonyl linker units for solid phase organic synthesis
No full textDiversity linker units exploit the cleavage step in solid phase synthesis for the incorporation of further diversity into target molecules. A solid-supported perfluorosulfonyl linker unit would allow cleavage of substrates using transition-metal- catalysed cross-coupling reactions. This thesis describes several approaches towards a perfluoroalkanesulfonyl diversity linker from diiodoperfluoroalkanes. Early work concentrated on the reaction of diiodoperfluoroalkanes with eugenol. The resulting perfluoroalkyliodides were attached to Wang resin using Mitsunobu chemistry. However, stability problems prevented the generation of resin bound perfluoroalkanesulfonic acids and the route was abandoned. A bis-perfluoroalkanesulfonyl chloride linker unit was prepared from diiodoperfluoroalkanes by generation of the bis-sodium sulfite salt and subsequent chlorination. Optimisation studies using design software allowed preparation of multigram quantities in 60 - 70% yield. Model solution phase synthesis of bis- perfluoroalkanesulfonamides and bis-perfluoroalkanesulfonate esters showed the feasibility of attaching the bis-sulfonyl chloride to amino resins and loading phenols. Diversity cleavage was demonstrated using Suzuki and Stille reactions and optimised by screening parallel arrays of reaction conditions. Loading the bis-sulfonyl chloride onto TentaGel® gave access to solid supported porfluorosulfonate osters and diversity cleavage was shown using Suzuki reactions. However, the linkage to solid supports proved to be unstable and an additional spacer unit was required if the linker was to find widespread use. To this end, a second generation perfluoroalkanesulfonyl linker unit was developed from ally I alcohol and diiodoperfluoroalkanes. Oxidation to a perfluoroalkanesulfonyl chloride was achieved using a novel reaction employing N- chlorosuccinimide. Several methods for loading this linker unit onto a solid support were investigated but none were successful and this chemistry requires further development before it offers a practical perfluoroalkanesulfonyl diversity linker
Dr. Duane M. Jackson, Morehouse College, July 2011
No full textThis video is a conversation with Dr. Duane M. Jackson. Dr. Jackson talks about his paper, "Recall and the Serial Position Effect: The Role of Primacy and Recency on Accounting Students' Performance." Jackie Daniel, AUC Woodruff Library, is the interviewer
"Reflections on the subject of Emigration from Europe with a view to Settlement in the United States" By M. Carey.
No full text"Reflections on the subject of Emigration from Europe with a view to Settlement in the United States: containing bried sketches of the moral and political character of those states.
By M. Carey, member of the American philosophical, and of the American Antiquarian Society, and author of The Olive Branch, Cindiciae Hibernicae, essays on banking, on political economy, and on internal improvement.
To which are now added the English editor's comments on the subject; together with Important Advice to Emigrants, and Cautions Against Impositions Practiced in the Outports
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