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1. |
Spectrophysics and photochemistry of the formaldehyde molecule. Part II |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 101,
Issue 7‐8,
1982,
Page 225-233
Henk M. Buck,
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ISSN:0165-0513
DOI:10.1002/recl.19821010701
出版商:WILEY‐VCH Verlag
年代:1982
数据来源: WILEY
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2. |
Phosphotriester synthesis of DNA fragments on cellulose and polystyrene solid supports |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 101,
Issue 7‐8,
1982,
Page 234-241
G. A. van der Marel,
J. E. Marugg,
E. de Vroom,
G. Wille,
M. Tromp,
C. A. A. van Boeckel,
J. H. van Boom,
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摘要:
AbstractThe synthesis of a total of twelve DNA fragments on the solid supports cellulose or polystyrene via a phosphotriester approach is described. Dimer and trimer blocks, protected at the 5′‐end with the levulinoyl group, were used for chain extension in the presence of the activating agent (2,4,6‐triisopropylbenzenesulfonyl)‐3‐nitro‐1,2,4‐triazole or (mesitylenesulfonyl)‐3‐nitro‐1,2,4‐triazole. The yields of the coupling procedures are normally high and the final unprotected DNA fragments released from the solid support could easily be isolated by Sephadex G50
ISSN:0165-0513
DOI:10.1002/recl.19821010702
出版商:WILEY‐VCH Verlag
年代:1982
数据来源: WILEY
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3. |
Solid‐phase synthesis of the RNA fragment: rAAGAAGAAGAAGA |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 101,
Issue 7‐8,
1982,
Page 241-246
G. A. van der Marel,
G. Wille,
J. H. van Boom,
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摘要:
AbstractThe synthesis of the tridecaribonucleotide AAGAAGAAGAAGA on a polystyrene solid support via a phosphotriester approach is described. The assemblage of the oligomer was performed by four repeated coupling reactions of the partially protected trimer AAGp(3′) with an immobilized dimer in the presence of the activating agent (2,4,6‐triisopropylbenzenesulfonyl)‐3‐nitro‐1,2,4‐triazole. Purification of the RNA fragment was easily achieved by Sephadex G50 column chr
ISSN:0165-0513
DOI:10.1002/recl.19821010703
出版商:WILEY‐VCH Verlag
年代:1982
数据来源: WILEY
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4. |
Studies on polypeptides XXXVII. Synthesis of [isoleucine‐13, homoserine‐20]‐s‐peptide lactone and semisynthesis of [isoleucine‐13, homoserine‐20]‐RNase A |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 101,
Issue 7‐8,
1982,
Page 246-253
P. Hoogerhout,
K. E. T. Kerling,
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摘要:
AbstractThe solid‐phase synthesis of [Ile13, Met20]‐S‐peptide‐(Gly‐Gly) on a Merrifield resin, using tert‐butoxycarbonyl‐ and benzyl‐type protecting groups, is reported. Deprotection was achieved by reaction with liquid hydrogen fluoride and purification by ion‐exchange chromatography and HPLC.The above peptide was converted into [Ile13, Hse20]‐S‐peptide lactone by reaction with cyanogen bromide. Reaction of the synthetic 20‐peptide lactone with “native” bovine S protein at pH 7.5 resulted in the formation of [Ile13, Hse20]‐RNase A in about 10% yield. The semisynthetic enzyme was purified by ion‐exchange chromatography and the kinetic parameters were deter
ISSN:0165-0513
DOI:10.1002/recl.19821010704
出版商:WILEY‐VCH Verlag
年代:1982
数据来源: WILEY
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5. |
Conformational analysis of an RNA triplet in aqueous solution: m62A‐U‐m62Astudied by two‐dimensional nuclear magnetic resonance at 500 MHz |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 101,
Issue 7‐8,
1982,
Page 253-263
Peter P. Lankhorst,
Cornelis M. Groeneveld,
Gerry Wille,
Jacques H. van Boom,
Cornelis Altona,
Cornelis A. G. Haasnoot,
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摘要:
AbstractThe complete assignment of the 18 ribose proton NMR signals of the trinucleoside diphosphate m62A(1)‐U(2)‐m62A(3) is given. The analysis was carried out by means of spin‐echo‐correlated spectroscopy and two‐dimensionalJ‐resolved spectroscopy at 500 MHz. Analysis of the chemical shifts and coupling constants demonstrates that the trimer does not form a classical right‐handed helix. Instead, the interior U(2) fragment appears to be “bulged‐out”, concomitant with a next‐nearest‐neighbour interaction between the terminal purine bases. An analogy with the behaviour of the first three residues in the tetramer m62A(1)‐U(2)‐m62A(3)‐U(4) is noted. An analysis of the coupling constants in terms of the N/S equilibrium and population distribution around the torsional degrees of freedom along the sugar‐
ISSN:0165-0513
DOI:10.1002/recl.19821010705
出版商:WILEY‐VCH Verlag
年代:1982
数据来源: WILEY
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6. |
Synthesis and reactivity of 22,23‐methylene‐2,3,17,18‐tetramethyl‐23‐hydro‐1, 19‐[21H,24H]‐bilindion‐10‐enium trifluoroacetate |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 101,
Issue 7‐8,
1982,
Page 263-266
J. A. de Groot,
R. van der Steen,
J. Lugtenburg,
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摘要:
AbstractThe biliverdinium salt 1 has been prepared in high yield and its behaviour towards nucleophiles studied. The reactions have been found to occur selectively on the central carbon atom 10 and to lead to bilirubin systems. In addition, the photoisomerisation of the bilirubin model compound 5, prepared from 1, has been investigated.
ISSN:0165-0513
DOI:10.1002/recl.19821010706
出版商:WILEY‐VCH Verlag
年代:1982
数据来源: WILEY
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7. |
Effect of pressure on the (2 + 2) cycloaddition of cyclopropanone diethyl acetal to tetracyanoethylene |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 101,
Issue 7‐8,
1982,
Page 267-269
Petrus G. Wiering,
Herbert Steinberg,
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摘要:
AbstractThe pressure dependence of the (2 + 2) cycloaddition of cyclopropanone diethyl acetal to tetracyanoethylene in methylene chloride and acetonitrile has been studied. The reaction is about ten times faster in the less polar methylene chloride in the pressure range 1‐2000 atm. The volume of activation is found to be ‐20.9 cm3/mole (CH2Cl2) and ‐24.5 cm3/mole (CH3CN). The estimated volume of the transition state is equal in both solvents and is of the same order of magnitude as the partial molar volume of the cycloadduct 1,1‐diethoxy‐2,2,3,3‐tetracyanocyclopentane. These findings are in agreement with a concerted cycloaddition mechanism via a weak complex of th
ISSN:0165-0513
DOI:10.1002/recl.19821010707
出版商:WILEY‐VCH Verlag
年代:1982
数据来源: WILEY
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8. |
A simple synthesis of glycino ethyl ester derivatives of hexachlorocyclotriphosphazene |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 101,
Issue 7‐8,
1982,
Page 270-271
A. A. Smaardijk,
B. de Ruiter,
A. A. van der Huizen,
J. C. van de Grampel,
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摘要:
AbstractA general method of preparation is described for glycino ethyl ester derivatives of phosphazene‐like ring systems, which may serve as precursors for anti‐cancer dr
ISSN:0165-0513
DOI:10.1002/recl.19821010708
出版商:WILEY‐VCH Verlag
年代:1982
数据来源: WILEY
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9. |
Intramolecular competition between the di‐π‐methane and the oxa‐di‐π‐methane rearrangements in a triplet‐excited β, γ, β1, γ1‐dienone. |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 101,
Issue 7‐8,
1982,
Page 272-273
Reinout van der Veen,
Cornelis Kruk,
Hans Cerfontain,
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摘要:
AbstractThe triplet photosensitization of the β, γ, β1, γ1‐dienone 2 leads to the formation of the DPM isomer 6 and the two ODPM isomers 7 and 8 in a ratio of 35:17:10. This is the first reported example of a substrate which exhibits intramolecular competition as demonstrated by the occurrence of both the DPM and ODPM rearrang
ISSN:0165-0513
DOI:10.1002/recl.19821010709
出版商:WILEY‐VCH Verlag
年代:1982
数据来源: WILEY
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10. |
Photochemical, transformations of tetracyclo [3. 3.0.02,4.03,6]OCT‐7‐ene |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 101,
Issue 7‐8,
1982,
Page 274-275
J. Stapersma,
G. W. Klumpp,
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摘要:
AbstractCyclooctatetraene is a common product of photolysis of the title compound la. Depending on reaction conditions it is accompanied by benzene (solvent: cyclohexane, γ = 253.7 nm), benzene plus semibullvalene (acetone, 300 nm), and an oxetane (cyclohexane, 350 nm, presence of an equimolar amount of benzophenone)
ISSN:0165-0513
DOI:10.1002/recl.19821010710
出版商:WILEY‐VCH Verlag
年代:1982
数据来源: WILEY
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