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1. |
Synthesis of thiahydrindanones and thiadecalones by Dieckmann cyclization: The stereochemistry of thiolate anion addition to cyclohexenes |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 92,
Issue 9,
1973,
Page 937-944
A. van Bruijnsvoort,
E. R. de Waard,
J. L. van Bruijnsvoort‐Meray,
H. O. Huisman,
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摘要:
AbstractThe synthesis oftrans‐3‐thiadecal‐1‐one (5) andcis‐3‐thiahydrindan‐1‐one (12) by Dieckmann cyclization (DC) is described. Anions of mercapto‐esters are shown to add to activated cyclohexenes in atransdiaxial fashion in kinetically controlled Michael additions (MA). An explanation is presented for the retro‐MA ofcis‐1‐(2î‐ethoxycarbonylethylthio)‐2‐ethoxycarbonylcycloh
ISSN:0165-0513
DOI:10.1002/recl.19730920902
出版商:WILEY‐VCH Verlag
年代:1973
数据来源: WILEY
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2. |
Pyrazoles and imidazoles as ligands. Part xviii: Neutral and anionic pyrazole coordinated to Cu(I) and Ag(I) |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 92,
Issue 9,
1973,
Page 945-953
H. Okkersen,
W. L. Groeneveld,
J. Reedijk,
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摘要:
AbstractA few compounds having the general formula M(L)+2X−are reported, in which M(I) = Cu or Ag, X−= BF−4, NO−3, Cl−, Br−, and L stands for pyrazole, 3(5)‐methylpyrazole and 4‐nitropyrazole. The compounds are formed by reaction of MX and L in acidic medium. Infrared spectra of the compounds are consistent with linear cations ML+2and uncoordinated anions.Apart from the above compounds, a different class of compounds is formed in less protic media. These compounds are salt like and have the formula M+L−, with M+= Cu+and Ag+and L = pyrazole, 4‐iodopyrazole, 4‐bromopyrazole, 4‐ethylpyrazole, 4‐nitropyrazole and 3(5)‐methylpyrazole.Infrared spectra, mass spectra, X‐ray powder diagrams and solubility studies indicate that these compounds are at least trimeric and possibly polymeric with bridging pyrazolate
ISSN:0165-0513
DOI:10.1002/recl.19730920903
出版商:WILEY‐VCH Verlag
年代:1973
数据来源: WILEY
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3. |
Chemistry of α‐nitrosulfones. Part I: Sulfinate elimination from α‐sulfonylnitroalkane anion radicals |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 92,
Issue 9,
1973,
Page 954-960
J. J. Zeilstra,
Jan B. F. N. Engberts,
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摘要:
AbstractElectron transfer reactions to 2‐nitropropylp‐tolyl sulfone (1) using different electron donors, are described. Using potassium 2‐propylnitronate as the electron donor, the product formation is proposed to occurviaa free radical chain process involving rapid elimination ofp‐toluenesulfinate anion from the anion radical derived from 1. When the carbon atom connecting the nitro and sulfonyl groups bears hydrogen, the corresponding α‐sulfonyl nitronate is formed as the only product under comparable conditions. Treatment of l‐iodo‐l‐nitro‐l‐(p‐tolylsulfonyl) propane with potassium 2‐propylnitronate in ethanol affords the potassium salt of l‐nitro‐l‐(p‐tolylsulfonyl) propane, 2,3‐dimethyl‐2,3‐dinitrobutane and iodine. Possible mechanisms for the formation o
ISSN:0165-0513
DOI:10.1002/recl.19730920904
出版商:WILEY‐VCH Verlag
年代:1973
数据来源: WILEY
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4. |
A study of π‐conjugation in Chichibabin's ‐ and Schlenk's ‐ like hydrocarbons with ESR: Part i |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 92,
Issue 9,
1973,
Page 961-969
By C. Kooistra,
J. M. F. van Dijk,
P. M. van Lier,
H. M. Buck,
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摘要:
AbstractAnalysis of the ESR spectrum of the radical cation, derived fromp,p′‐bis‐{phenyl(triphenylphosphorylidene)methyl}biphenyl reveals that spin density is found at both31P nuclei. Zero spin density is indicated for the outer phenyl rings. In the radical cation, derived from the correspondingm,m′‐isomer the spin density is delocalized over one half of the molecule and interaction is found with only one phosphorus atom. In this system the spin density in the outside ring exceeds that in the biphenyl ring. The localization of the odd electron on one half of the molecule must be caused by a strong Jahn‐Teller effect.The assignment of the hyperfine coupling constants was based on spin density calculations according to the Unrestricted Hartree‐Fock (UHF) method. From these calculations we also obtained an indication of the geometry of the radicals.The synthesis of these compound
ISSN:0165-0513
DOI:10.1002/recl.19730920905
出版商:WILEY‐VCH Verlag
年代:1973
数据来源: WILEY
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5. |
Reactivity of derivatives of 3‐bromo‐l, 5‐naphthyridine and 3‐bromoquinoline towards potassium amide in liquid ammonia |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 92,
Issue 9,
1973,
Page 970-976
J. Pomorski,
H. J. den Hertog,
D. J. Buurman,
N. H. Bakker,
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摘要:
AbstractReactions of some 2‐substituted derivatives of 3‐bromo‐l, 5‐naphthyridine and 3‐bromoquinoline with potassium amide in liquid ammonia were investigated. The course of these aminations is compared with that of corresponding processes studied p
ISSN:0165-0513
DOI:10.1002/recl.19730920906
出版商:WILEY‐VCH Verlag
年代:1973
数据来源: WILEY
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6. |
Les sulfates acides de manganèse: I. L'hydrogénosulfate |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 92,
Issue 9,
1973,
Page 977-984
Par G. Palavit,
S. Noël,
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摘要:
AbstractThe manganese hydrogenosulfat is prepared according to the ternary diagram MnSO4‐H2SO4,‐H2O. It crystallizes in the spatial groups P21/cwith two molecules in the cell. A frequences' attribution of the group HSO4is proposed. From a thermal study, the hypothesis of a decomposition mechanism can be propo
ISSN:0165-0513
DOI:10.1002/recl.19730920907
出版商:WILEY‐VCH Verlag
年代:1973
数据来源: WILEY
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7. |
Vilsmeier formylation of vinylcyclopropanes: 1. Formylation of thujopsene |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 92,
Issue 9,
1973,
Page 985-995
P. C. Traas,
H. Boelens,
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摘要:
AbstractThujopsene(1)can be formylated in the 3‐position in 80% yield by use of one equivalent of the Vilsmeier reagent. The resulting 3‐formylthujopsene(4)is useful for the synthesis of other 3‐substituted derivatives (CH2OH, COOH, COCH3). With an excess of the reagent higher formylation products are formed. Two such products have been isolated and characterized and a mechanism for their formation is put fo
ISSN:0165-0513
DOI:10.1002/recl.19730920908
出版商:WILEY‐VCH Verlag
年代:1973
数据来源: WILEY
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8. |
A spectroscopic study of zinc(II), cadmium(II) and mercury(II) complexes with tricyclohexylphosphine as ligand |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 92,
Issue 9,
1973,
Page 996-1002
F. G. Moers,
J. P. Langhout,
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摘要:
AbstractThe preparations of the complexes M(PCy3)2X2and M(PCy3)X2with M = Zn, Cd or Hg, X = Cl, Br, I or SCN, PCy3= tricyclohexylphosphine and some of their adducts with acetone, methanol or carbon disulfide are reported. Their infrared spectra in the range 4000‐200 cm−1and their Raman spectra between 4000‐100 cm−1have been investigated. From these data we conclude for the dimeric complexes M(PCy3)X2with M = Cd or Hg and X = Cl, Br or I, a distorted tetrahedral coordination around mercury or cadmium. For the complex Hg(PCy3)(SCN)2we suggest a trigonal coordination around mercury. Assignments are proposed for the metal‐halogen and metal‐phosphorus
ISSN:0165-0513
DOI:10.1002/recl.19730920909
出版商:WILEY‐VCH Verlag
年代:1973
数据来源: WILEY
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9. |
Conformation of non‐aromatic ring compounds‐80: Calculation of dihedral angles from vicinal proton coupling constants in mono‐ and di‐substituted glutaric anhydrides |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 92,
Issue 9,
1973,
Page 1003-1014
F. J. Koer,
T. M. W. van Asbeck,
C. Altona,
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摘要:
AbstractThe Lambert‐Buys R‐value method is applied to several six‐membered α‐mono‐α,α‐ andtrans‐α,α′‐di‐substituted glutaric anhydrides. A discussion concerning the appearance of the AA′BB′ spectra of the compounds under consideration is given. The vicinal proton coupling constantsJtrans(7.3‐8.1 Hz) andJcis(4.9‐6.4 Hz) and the corresponding ring dihedral angles (ψ: 49°‐53°) are reported. The results are interpreted in terms of small deformations of the “sofa” conformation
ISSN:0165-0513
DOI:10.1002/recl.19730920910
出版商:WILEY‐VCH Verlag
年代:1973
数据来源: WILEY
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10. |
PMR‐spectra of some diastereoisomeric ionol isomers in the presence of EUIII‐2,2,6,6‐tetramethylheptadionate |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 92,
Issue 9,
1973,
Page 1015-1019
C. Kruk,
A. A. M. Roof,
A. van Wageningen,
H. Cerfontain,
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摘要:
AbstractPMR‐spectra of diastereoisomers containing two chiral centres can be elucidated by complexation with the EuIII‐heptadionate shift reagent, as is illustrated for the two pairs of diastereoisomers of both(E)‐α‐ionol (I) and the bicyclic
ISSN:0165-0513
DOI:10.1002/recl.19730920911
出版商:WILEY‐VCH Verlag
年代:1973
数据来源: WILEY
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