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1. |
The synthesis of oligoribonucleotides VI. The synthesis of a hexadecamer by a block condensation approach |
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Canadian Journal of Chemistry,
Volume 58,
Issue 14,
1980,
Page 1389-1397
Kelvin K. Ogilvie,
Mona J. Nemer,
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摘要:
The synthesis of the 5′-monomethoxytrityl-2′-tert-butyldimethylsilyl-3′-levulinylribonucleosides4of the four major bases involved in the phosphite procedure for the synthesis of oligoribonucleotides is described along with the 2′,3′-isomeric derivatives6. This report describes a total protection system for nucleotide units which allows for the block condensation procedure to be used for the synthesis of long chains. The procedure is illustrated by the synthesis of a hexadecauridylic acid.
ISSN:0008-4042
DOI:10.1139/v80-219
出版商:NRC Research Press
年代:1980
数据来源: NRC
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2. |
The synthesis and reactions of 2,11-diselena[3,3]metacyclophanes. An investigation of the selenoxide elimination route to metacyclophane-1,8-dienes |
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Canadian Journal of Chemistry,
Volume 58,
Issue 14,
1980,
Page 1398-1406
Reginald H. Mitchell,
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摘要:
2,11-Diselena[3,3]metacyclophane and its 9,18-dimethyl derivative are prepared in ca. 7% yield from Na2Se and xylylene bromide. Wittig rearrangement and benzyne induced Stevens rearrangement gave the ring contracted [2,2]metacyclophane derivative. Attempted selenoxide elimination to produce metacyclophane-diene failed. The1Hmr spectra of the selenametacyclophane indicate that thesyn-conformer is the more stable. A general synthesis of aryl-alkenes in an 80% yield starting from benzyl phenyl selenide, alkylation with an alkyl halide, and then selenoxide elimination is given.
ISSN:0008-4042
DOI:10.1139/v80-220
出版商:NRC Research Press
年代:1980
数据来源: NRC
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3. |
Complex fluoroanions in solution. XI. Complexes of silicon, germanium, and titanium tetrafluorides with simple anions |
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Canadian Journal of Chemistry,
Volume 58,
Issue 14,
1980,
Page 1407-1411
S. Brownstein,
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摘要:
A fluorine-bridged silicon fluoroanion and many hexa-co-ordinate germanium and titanium fluoroanions have been identified in solution via fluorine magnetic resonance. A generalized shceme is used to correlate all fluorine chemical shift data for hexa-coordinate fluorine containing species.
ISSN:0008-4042
DOI:10.1139/v80-221
出版商:NRC Research Press
年代:1980
数据来源: NRC
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4. |
Potentiometric properties of trialkylammonium ion-exchangers |
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Canadian Journal of Chemistry,
Volume 58,
Issue 14,
1980,
Page 1412-1417
Michel Gérin,
James Fresco,
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摘要:
The potentiometric behaviour of nitrobenzene solutions of 21 trialkylammonium salts employed as membrane material has been investigated. Deviations from ideal Nernst response curves for chloride, bromide, iodide, and perchlorate sensors were explicable on the basis of partition and hydrolysis of the ion exchangers. Interference coefficients for the anion selective electrochemical sensor tridodecylammonium perchlorate could be related to the ion-exchange constant of the salt.
ISSN:0008-4042
DOI:10.1139/v80-222
出版商:NRC Research Press
年代:1980
数据来源: NRC
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5. |
Octahedral–tetrahedral equilibria in aqueous cobalt(II) solutions at high temperatures |
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Canadian Journal of Chemistry,
Volume 58,
Issue 14,
1980,
Page 1418-1426
Thomas Wilson Swaddle,
Leonard Fabes,
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摘要:
Evidence is presented to indicate that aqueous Co2+exists as the hexaaquo-ion in equilibrium with minor amounts (upper limits 0.08% at 298 K, 7% at 625 K, at 16–25 MPa) of tetraaquocobalt(II), with ΔH ~ +17 kJ mol−1. The single visible absorption band of the supposed Co(H2O)42+has maxima at 552 nm and 486 nm in the intensity ratio 2:1. Hydrogen sulfate ion (up to 0.5 Mat least) does not complex Co2+(aq) detectably in acidic media, 290–625 K, and sulfuric acid therefore holds promise as a non-complexing strong monobasic acid for high-temperature aqueous studies. In water containing 2.0 Mor more Cl−, the tetrahedral form of cobalt(II) is CoCl42−, ΔHfor the octahedral → tetrahedral equilibrium being +62 kJ mol−1; forCoBr42−, the corresponding ΔHis +70 kJ mol−1, the greater endothermicity accounting entirely for the lower stability relative to CoCl42−.
ISSN:0008-4042
DOI:10.1139/v80-223
出版商:NRC Research Press
年代:1980
数据来源: NRC
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6. |
Total synthesis of 3,17β-dihydroxy-6-oxaestra-1,3,5(10),7-tetraen and related miroestrol analogues |
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Canadian Journal of Chemistry,
Volume 58,
Issue 14,
1980,
Page 1427-1434
John A. Findlay,
Paul Mebe,
Michael D. Stern,
M. L. Givner,
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摘要:
3,17β-Dihydroxy-6-oxaestra-1,3,5(10),7-tetraen and related steroidal compounds have been synthesized in high yield via condensation of 7-methoxy-4-vinyl coumarin and 2-methyl-1,3-pentanedione. The approximate uterotrophic activity of the synthetic compounds relative to 17β-estradiol has been determined.
ISSN:0008-4042
DOI:10.1139/v80-224
出版商:NRC Research Press
年代:1980
数据来源: NRC
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7. |
Azole derivatives of metals. VI. Binuclear platinum(II) derivatives having both μ-pyrazolato-N,N′ and methoxy or chloride as bridging groups |
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Canadian Journal of Chemistry,
Volume 58,
Issue 14,
1980,
Page 1435-1438
Flavio Bonati,
Howard C. Clark,
Chun S. Wong,
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摘要:
Binuclear platinum(II) complexes of the typewhere X = H, CH3, Y = H, Br, Z = Cl, OCH3, are synthesized by the reaction of Pt2Cl4(PEt3)2with the pyrazole and sodium hydroxide in methanol. The nature of the product depends on the amount of sodium hydroxide used.
ISSN:0008-4042
DOI:10.1139/v80-225
出版商:NRC Research Press
年代:1980
数据来源: NRC
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8. |
Metal binding to N(9), N(7), and N(3) of adenine. Crystal structure of μ-(adeninato-N3,N7,N9)tris(methylmercury(II)) perchlorate |
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Canadian Journal of Chemistry,
Volume 58,
Issue 14,
1980,
Page 1439-1443
Joseph Hubert,
André L. Beauchamp,
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摘要:
The title compound belongs to space groupwith the following cell parameters:a = 6.304,b = 11.925,c = 25.946 Å, α = 85.76, β = 89.78, γ = 83.57°, andZ = 4. The structure was solved by the heavy-atom method and refined on 2570 nonzero reflections to anRfactor of 0.044. In the two crystallographically independent [Adeninato(CH3Hg)3]2+ions, methylmercury groups are linearly bonded to N(3), N(7), and N(9) of a deprotonated adenine ring, forming Hg—N bonds of normal lengths (ave. 2.08 Å) for two-coordinated mercury. One half of the complex cations are associated in a dimeric unit by a pair of stronghydrogen bonds, while the others are packed as individual species in the crystal. The structure is stabilized by a number of contacts between mercury and perchlorate oxygens.
ISSN:0008-4042
DOI:10.1139/v80-226
出版商:NRC Research Press
年代:1980
数据来源: NRC
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9. |
The crystal structure of the neuroleptic agent (±)-deoxybutaclamol and its significance for the topography of the central dopamine receptor |
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Canadian Journal of Chemistry,
Volume 58,
Issue 14,
1980,
Page 1444-1448
S. Fortier,
M. Przybylska,
L. G. Humber,
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摘要:
(±)-Deoxybutaclamol, C25H31N, crystallizes in space groupP21/awith cell dimensions:a = 16.626(3),b = 10.646(2),c = 11.278(3) Å, β = 90.47(4)°. The structure was solved by direct methods using the QTAN program. The coordinates were refined by block-diagonal least-squares calculations toR = 0.052 for 3147 observed reflections.The structure of (±)-deoxybutaclamol was found to be very similar to that of equipotent (±)-butaclamol and is in agreement with that assigned on the basis of chemical, spectral, crystallographic, and pharmacological studies. This confirmation validates the coordinates of a lipophilic accessory binding site in a proposed model of the central dopamine receptor.
ISSN:0008-4042
DOI:10.1139/v80-227
出版商:NRC Research Press
年代:1980
数据来源: NRC
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10. |
Aromatic fluorination with xenon difluoride:L-3,4-dihydroxy-6-fluoro-phenylalanine |
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Canadian Journal of Chemistry,
Volume 58,
Issue 14,
1980,
Page 1449-1450
Gunter Firnau,
Raman Chirakal,
Sudesh Sood,
Stephen Garnett,
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摘要:
L-3-Methoxy-4-hydroxyphenylalanine was fluorinated directly with XeF2in CH2Cl2at −60 °Cinvacuo. After hydrolysis with 48% aqueous HBr,L-6-fluorodopa was obtained. The yield, based on XeF2, was 25%. This reaction might be applied when chiral biomolecules are to be tagged with fluorine-18.
ISSN:0008-4042
DOI:10.1139/v80-228
出版商:NRC Research Press
年代:1980
数据来源: NRC
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