142,710 research outputs found
A Tripartite Post-Recession Rebalancing
No full textIn this latest Advance & Rutgers Report, entitled “A Tripartite Post-Recession Rebalancing,” Dean James W. Hughes and Professor Joseph J. Seneca deliver an incisive assessment of the current market conditions and obstacles in the path of our economic recovery. They offer a statistical cautionary tale that the private and public sector need to hear and acknowledge in order for the economy to make continued progress.This report was published as Issue Paper Number 7, November 2011, in Advance & Rutgers Report
Transformation of phenylchlorodiazirines to 1,3-dioxolanes and a 1,3-dithiolane
No full textPT: J; CR: FREIDRICH K, 1985, TETRAHEDRON LETT, V26, P193 GRAHAM WH, 1965, J AM CHEM SOC, V87, P4396 GRILLER D, 1982, J AM CHEM SOC, V104, P5549 GRILLER D, 1983, J ORG CHEM, V48, P1359 INDICTOR N, 1969, J CHEM ENG DATA, V14, P76 KIRMSE W, 1971, CARBENE CHEM KIRMSE W, 1981, J AM CHEM SOC, V103, P5935 LIU MTH, 1972, CAN J CHEM, V50, P3009 LIU MTH, 1984, J CHEM SOC CHEM COMM, P1062 LIU MTH, 1984, TETRAHEDRON, V40, P887 MOSS RA, 1973, CARBENES, V1 MOSS RA, 1975, CARBENES, V2 MOSS RA, 1984, TETRAHEDRON LETT, V25, P1023 STEINBECK K, 1979, CHEM BER, V112, P2402 WARNER P, 1984, J ORG CHEM, V49, P3666; NR: 15; TC: 0; J9: HETEROCYCLES; PG: 5; GA: AVW79Source type: Electronic(1
Time-resolved Systems Immunology Reveals a Late Juncture Linked to Fatal COVID-19. Liu et al
No full textSupplemental Tables 1-7 for the paper: Can Liu, Andrew J. Martins, William W. Lau, Nicholas Rachmaninoff, ..., John S. Tsang. (2021). "Time-resolved Systems Immunology Reveals a Late Juncture Linked to Fatal COVID-19." Cell. In Press
1, 2-H shift in benzylchlorocarbene: isotope effect and influence of the solvent
No full textLaser flash photolysis of 3-chloro-3-benzyldiazirine and 3-chloro-3-(phenyldideuteriomethyl)diazirine in isooctane over the 60 to -80-degrees-C temperature range gives rise to curved Arrhenius plots for both 1,2-H and 1,2-D migration in benzylchlorcarbene. The k(H)/k(D) values increase smoothly from 0.87 to 2.62 when the temperature increases from -60 to +30-degrees-C. The k(H)/k(D) value is approximately 4 for most of the temperatures studied if a solvent correction is applied. Quantum mechanical tunnelling or the influence of the solvent may be a possible explanation for these observations.PT: J; CR: BONNEAU R, 1989, J AM CHEM SOC, V111, P5973 BONNEAU R, 1992, J PHOTOCH PHOTOBIO A, V68, P97 DIX EJ, 1993, J AM CHEM SOC, V115, P10424 EVANSECK JD, 1990, J PHYS CHEM-US, V94, P5518 GRAHAM WH, 1965, J AM CHEM SOC, V87, P4396 JACKSON JE, 1994, ADV CARBENE CHEM JONES M, 1980, REACTIVE INTERMEDIAT, V2 KIRMSE W, 1971, CARBENE CHEM LIU MTH, 1984, TETRAHEDRON, V40, P887 LIU MTH, 1990, J AM CHEM SOC, V112, P3915 LIU MTH, 1992, J PHOTOCH PHOTOBIO A, V63, P115 LIU MTH, 1992, J PHYS ORG CHEM, V15, P285 LIU MTH, 1994, RES CHEM INTERMEDIAT, V20, P195 MODARELLI DA, 1992, J AM CHEM SOC, V114, P7034 MOSS RA, 1992, TETRAHEDRON LETT, V33, P4287 MOSS RA, 1994, ADV CARBENE CHEM MUROV SL, 1973, HDB PHOTOCHEMISTRY NICKON A, 1993, ACCOUNTS CHEM RES, V26, P84 SALIS GA, 1968, J PHYS CHEM-US, V72, P752 SANDER W, 1994, UNPUB SCHAEFER HF, 1979, ACCOUNTS CHEM RES, V12, P288 SCHOLLER WW, 1989, HOUBEN WEYL METHODEN, P41 SHIMANOUCHI T, 1972, TABLES MOL VIBRATION, V1 SUGIYAMA MH, 1992, J AM CHEM SOC, V114, P966 WIERLACHER S, 1993, J AM CHEM SOC, V115, P8943; NR: 25; TC: 20; J9: J PHOTOCHEM PHOTOBIOL A-CHEM; PG: 5; GA: PV021Source type: Electronic(1
Carboxylation of carbenes in low-temperature matrixes
No full textPT: J; CR: ADAM W, 1971, J AM CHEM SOC, V93, P557 ADAM W, 1973, J ORG CHEM, V38, P2269 BAMFORD WR, 1952, J CHEM SOC, P4735 BONNEAU R, 1989, J CHEM SOC CHEM COMM, P510 CHAMPAM OL, 1972, J AM CHEM SOC, V94, P1365 COE PL, 1982, J CHEM SOC CHEM COMM, P362 EISENTHAL KB, 1985, TETRAHEDRON, V41, P1543 GANZER GA, 1986, J AM CHEM SOC, V108, P1517 GOULD IR, 1985, TETRAHEDRON, V41, P1587 GRAHAM WH, 1965, J AM CHEM SOC, V87, P4396 GRILLER D, 1985, TETRAHEDRON, V41, P1525 LIU MTH, 1980, J CHEM SOC CHEM COMM, P1482 LIU MTH, 1987, TETRAHEDRON LETT, V28, P1011 MALTSEV AK, 1985, IAN SSSR KH, P2159 MCMAHON RJ, 1987, J AM CHEM SOC, V109, P2456 MILLIGAN DE, 1962, J CHEM PHYS, V35, P2911 MOSS RA, 1989, ACCOUNTS CHEM RES, V22, P15 PLATZ MS, 1990, KINETICS SPECTROSCOP, P239 PUZA M, 1971, SYNTHESIS-STUTTGART, P481 SANDER W, 1988, ANGEW CHEM INT EDIT, V27, P572 SANDER W, 1988, ANGEW CHEM, V100, P577 SANDER W, 1988, J ORG CHEM, V53, P2091 SANDER W, 1990, ANGEW CHEM INT EDIT, V29, P344 SANDER W, 1990, ANGEW CHEM, V102, P362 SANDER WW, 1987, SPECTROCHIM ACTA A, V43, P637 SANDER WW, 1989, J ORG CHEM, V54, P333 SANDER WW, 1989, J ORG CHEM, V54, P4265 SIEBRAND W, 1986, ACCOUNTS CHEM RES, V19, P238 WHELAND R, 1970, J AM CHEM SOC, V92, P6057; NR: 29; TC: 22; J9: J ORG CHEM; PG: 3; GA: HB875Source type: Electronic(1
MNDO calculations on diazirines
No full textPT: J; CR: ARCHER WH, 1976, J CHEM SOC F1, V72, P1448 BIGOT B, 1978, IUPAC S PHOTOCHEMIST, P46 BINKLEY JS, QPCE368 BRADLEY GF, 1977, J CHEM SOC P2, P1214 BRASLAVSKY S, 1977, CHEM REV, V77, P473 BURKHOLDER D, J AM CHEM SOC CLOUGH PN, 1970, CAN J CHEM, V48, P2919 DEWAR MJS, J AM CHEM SOC, V99, P4999 DEWAR MJS, 1977, J AM CHEM SOC, V99, P4907 DEWAR MJS, 1978, J AM CHEM SOC, V100, P3607 DEWAR MJS, 1978, J AM CHEM SOC, V100, P777 ENGLEBRECHT WJ, 1975, JS AFRICAN CHEM I, V28, P191 FIGUERA JM, 1978, J CHEM SOC F1, P809 FREY HM, 1966, ADV PHOTOCHEM, V4, P225 FREY HM, 1977, J CHEM SOC F1, P2010 GILBERT JC, 1979, TETRAHEDRON LETT, P4619 HEHRE WJ, 1972, J CHEM PHYS, V56, P2257 HENCHER JL, 1967, J AM CHEM SOC, V89, P5527 JENNINGS BM, 1976, J AM CHEM SOC, V98, P6416 JONES M, 1973, CARBENES, V1 JONES WE, 1973, CHEM REV, V73, P407 JONES WE, 1976, J PHOTOCHEM, V5, P311 JONES WE, 1978, J CHEM SOC F2, V74, P831 LATHAN WA, 1973, FORTSCHR CHEM FORSCH, V40, P1 LAU A, 1964, SPECTROCHIM ACTA, V20, P97 LIU MTH, 1973, CAN J CHEM, V51, P2393 LIU MTH, 1977, CAN J CHEM, V55, P3596 MARTIN M, 1976, REV ROUM CHIM, V21, P31 MEIER H, 1977, ANGEW CHEM INT EDIT, V16, P835 MOFFAT JB, 1978, CHEM DIAZONIUM DIA 1 MOFFAT JB, 1979, J MOL STRUCT, V52, P275 NEWTON MD, 1970, J CHEM PHYS, V52, P4064 PIERCE L, 1962, J AM CHEM SOC, V84, P2651 PITTMAN CU, 1974, J ORG CHEM, V39, P373 SCHARPEN LH, 1969, J CHEM PHYS, V50, P2063 SCHMITZ E, 1964, ANGEW CHEM INT EDIT, V3, P333 SCHMITZ E, 1971, 23RD INT C PUR ALL C, V2, P283 SMITH NP, 1979, J CHEM SOC P2, P213 SNYDER LC, 1969, J AM CHEM SOC, V91, P2189 THIEL W, QCPE353 WOLLRAB JE, 1968, J CHEM PHYS, V49, P2405 WOLLRAB JE, 1969, J CHEM PHYS, V51, P1584 YURTSEVER E, 1974, CHEM PHYS LETT, V25, P605; NR: 43; TC: 5; J9: THEOR CHIM ACTA; PG: 7; GA: JW621Source type: Electronic(1
Reaction of benzylchlorocarbene with hydrogen chloride
No full textPT: J; CR: BROWN HC, 1942, J AM CHEM SOC, V64, P2223 BUSSEY RJ, 1969, J ORG CHEM, P1323 CLOSS GL, 1962, J AM CHEM SOC, V84, P4350 COCIVERA M, 1963, J AM CHEM SOC, V85, P1702 GRAHAM WH, 1965, J AM CHEM SOC, V87, P4396 KIRMSE W, 1971, CARBENE CHEM LIU MTH, 1981, J CHEM SOC P2, P53 LIU MTH, 1982, CHEM SOC REV, V11, P127 LIU MTH, 1984, J CHEM SOC CHEM COMM, P1062 LIU MTH, 1984, TETRAHEDRON, V40, P887 MOSS RA, 1973, CARBENES, V1 MOSS RA, 1975, CARBENES, V2; NR: 12; TC: 5; J9: J ORG CHEM; PG: 3; GA: APQ51Source type: Electronic(1
Detection of carbonyl oxide from singlet para-nitrophenylchlorocarbene and oxygen
No full textPT: J; CR: BARTLETT PD, 1962, J AM CHEM SOC, V84, P3408 BELL GA, 1985, SPECTROCHIM ACTA A, V41, P1221 BONNEAU R, 1989, J CHEM SOC CHEM COMM, P510 CARMICHAEL I, 1986, J PHYS CHEM REF DATA, V15, P1 CASAL HL, 1984, J AM CHEM SOC, V106, P7623 DUNKIN IR, 1986, J CHEM SOC CHEM COMM, P154 FESSENDEN RW, 1985, CHEM PHYS LETT, V117, P103 GANZER GA, 1986, J AM CHEM SOC, V108, P1517 GOULD IR, 1985, TETRAHEDRON, V41, P1987 HARDING LB, 1978, J AM CHEM SOC, V100, P7180 HULL LA, 1978, J ORG CHEM, V43, P2780 KIRMSE W, 1971, CARBENE CHEM KIRMSE W, 1985, CHEM BER, V19, P614 LIU MTH, 1987, CHEM DIAZIRINES, CH5 MOSS RA, 1986, J AM CHEM SOC, V108, P7028 PADWA A, 1969, J ORG CHEM, V34, P2728 SANDER W, 1985, ANGEW CHEM INT EDIT, V24, P988 SANDER W, 1985, ANGEW CHEM, V97, P964 SANDER W, 1986, ANGEW CHEM INT EDIT, V25, P255 SANDER W, 1988, J ORG CHEM, V53, P121 SANDER W, 1988, J ORG CHEM, V53, P2091 SANDER W, 1989, J ORG CHEM, V54, P335 SANDER WW, 1987, SPECTROCHIM ACTA A, V43, P637 SOUNDARARAJAN N, 1988, J AM CHEM SOC, V110, P7143 SUGAWARA T, 1983, CHEM LETT, P1261 TROZZOLO AM, 1962, J AM CHEM SOC, V84, P4990 TROZZOLO AM, 1968, ACCOUNTS CHEM RES, V1, P329 WADT WR, 1975, J AM CHEM SOC, V97, P244 WERSTIUK NH, 1984, CAN J CHEM, V62, P2391; NR: 29; TC: 17; J9: J CHEM SOC CHEM COMMUN; PG: 2; GA: EG981Source type: Electronic(1
Study of 1, 2-chlorine migration in (Alpha,alpha-dichlorobenzyl) chlorocarbene generated by laser flash photolysis of 3-chloro-3-(Alpha,alpha-dichlorobenzyl) diazirine
No full textPT: J; CR: BONNEAU R, 1989, J AM CHEM SOC, V111, P5973 GRAHAM WH, 1965, J AM CHEM SOC, V87, P4396 JONES M, 1973, CARBENES, V1 JONES M, 1975, CARBENES, V2 JONES WM, 1980, REARRANGEMENTS GROUN, V1 KIRMSE W, 1971, CARBENE CHEM LAVILLA JA, 1989, J AM CHEM SOC, V111, P6877 LIU MTH, IN PRESS J PHOTOCHEM LIU MTH, IN PRESS J PHYS ORG LIU MTH, 1987, CHEM DIAZIRINES LIU MTH, 1989, J AM CHEM SOC, V111, P6873 LIU MTH, 1990, J AM CHEM SOC, V112, P3915 LIU MTH, 1990, J CHEM SOC CHEM COMM, P1650 MORGAN S, 1991, J AM CHEM SOC, V113, P2782 MOSS RA, 1990, J AM CHEM SOC, V112, P5642 REGITZ M, 1989, METHODEN ORGANISCH E, V19 SCHAEFER HF, 1979, ACCOUNTS CHEM RES, V12, P288; NR: 17; TC: 4; J9: J ORG CHEM; PG: 3; GA: HN858Source type: Electronic(1
Measurement of the absolute rate of 1,2-hydrogen migration in benzylchlorocarbene
No full textPT: J; CR: ALTMANN JA, 1974, J AM CHEM SOC, V96, P4196 ALTMANN JA, 1975, J AM CHEM SOC, V97, P5217 BODOR N, 1972, J AM CHEM SOC, V94, P9103 GOULD IR, 1985, TETRAHEDRON, V41, P1587 GRAHAM WH, 1965, J AM CHEM SOC, V87, P4396 GRILLER D, 1982, J AM CHEM SOC, V104, P5549 JACKSON JE, 1988, J AM CHEM SOC, V110, P5595 JONES M, 1980, REACTIVE INTERMEDIAT, V2 JONES WM, 1987, REARRANGEMENTS GROUN, V1, CH8 KIRMSE W, 1971, CARBENE CHEM KYBA EP, 1977, J AM CHEM SOC, V99, P8330 LEOPOLD DG, 1984, J CHEM PHYS, V81, P1048 LIU MTH, 1985, J CHEM SOC CHEM COMM, P982 LIU MTH, 1986, J PHYS CHEM-US, V90, P75 MCKELLAR ARW, 1983, J CHEM PHYS, V79, P5265 MOSS RA, 1980, ACCOUNTS CHEM RES, V13, P58 MURRAY KK, 1988, J CHEM PHYS, V89, P5442 NOBES RH, 1980, CHEM PHYS LETT, V74, P269 RAGHAVACHARI K, 1982, CHEM PHYS LETT, V85, P145 SCHAEFER HF, 1979, ACCOUNTS CHEM RES, V12, P288 SOUNDARARAJAN N, 1988, J AM CHEM SOC, V110, P7143 STEVENS IDR, 1988, TETRAHEDRON LETT, V30, P481 SU DTT, 1978, J AM CHEM SOC, V100, P1872 TOMIOKA H, 1984, J AM CHEM SOC, V106, P454 TOMIOKA H, 1984, J CHEM SOC CHEM COMM, P476 WARNER PM, 1984, TETRAHEDRON LETT, V25, P4211; NR: 26; TC: 56; J9: J AMER CHEM SOC; PG: 2; GA: AM216Source type: Electronic(1
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