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1. |
Ring transformations andtele‐aminations in the reaction of 2‐halogeno‐ and 8‐halogeno‐1,7‐naphthyridines by potassium amide in liquid ammonia |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 96,
Issue 6,
1977,
Page 151-155
H.C. van der Plas,
M. Wózniak,
A. van Veldhuizen,
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摘要:
Abstract2‐X‐1,7‐Naphthyridines (X = Br, Cl) give a variety of products on treatment with potassium amide, namely 2‐amino‐1,7‐naphthyridine [formed by an SN(AE) process], 4‐amino‐ and 8‐amino‐1,7‐naphthyridine (obtained by atele‐amination[5N(AE)t]) and a ring transformed product, 2‐methyl‐4‐amino‐1,3,7‐triazanaphthalene. By1H‐NMR spectroscopy of a solution of 2‐chloro‐1,7‐naphthyridine and its 8‐deutero‐ and 6,8‐dideutero derivatives in KNH2/NH3good evidence has been obtained that at −40° 2‐chloro‐1,7‐naphthyridine is completely converted into a mixture of three 1 : 1 adducts formed by addition of the amide ion at C(8), C(6) and C(4). 8‐X‐1,7‐Naphthyridines (X = Cl, Br) give as sole reaction products 8‐amino‐1,7‐naphthyridine [5N(AE)] and 2‐amino‐1,7‐naphthyridine [5N(AE)t]. By1H‐NMR spectroscopy strong evidence has been obtained that in 8‐X‐1,7‐naphthyridines the adduct for
ISSN:0165-0513
DOI:10.1002/recl.19770960602
出版商:WILEY‐VCH Verlag
年代:1977
数据来源: WILEY
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2. |
Photochemistry ofN‐benzoyliminopyrimidines |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 96,
Issue 6,
1977,
Page 156-157
F. Roeterdink,
H.C. van der Plas,
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ISSN:0165-0513
DOI:10.1002/recl.19770960603
出版商:WILEY‐VCH Verlag
年代:1977
数据来源: WILEY
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3. |
The photo‐oxidation of hexamethylbenzene by singlet oxygen |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 96,
Issue 6,
1977,
Page 157-159
C.J.M. van den Heuvel,
H. Steinberg,
Th.J. de Boer,
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摘要:
AbstractIn the dye‐sensitized photo‐oxidation of hexamethylbenzene two molecules of singlet oxygen are rapidly taken up: one of the oxygenation steps involved is an ene‐type reaction, and the other a [4 + 2]‐cycloaddition. The resulting endoperoxy hydroperoxide2can be reduced selectively to the corresponding endoperoxy alcohol3and by further reduction to the triol4. X‐ray analysis shows the hydroperoxy group and the OO bridge in2to be on different sides of the cycl
ISSN:0165-0513
DOI:10.1002/recl.19770960604
出版商:WILEY‐VCH Verlag
年代:1977
数据来源: WILEY
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4. |
A modified procedure for the isomerization of alkynes and acetylenic alcohols to terminal acetylenes: (Preliminary communication) |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 96,
Issue 6,
1977,
Page 160-160
H. Hommes,
L. Brandsma,
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ISSN:0165-0513
DOI:10.1002/recl.19770960605
出版商:WILEY‐VCH Verlag
年代:1977
数据来源: WILEY
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5. |
Réarrangement de dérivés des thiolannones‐2 |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 96,
Issue 6,
1977,
Page 161-168
G. Brisset,
L. Morin,
D. Paquer,
P. Rioult,
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摘要:
AbstractVarious nucleophiles (sodium methoxide, hydride ion, thiolates and carbanions derived from organomagnesium compounds and ketones) react with 3‐[bis(methylthio)methylene]‐2‐thiolanones giving a rearrangement. The mechanism of the proposed rearrangement has been investigated. The reaction of enolate ions with thiolanones produces new β‐d
ISSN:0165-0513
DOI:10.1002/recl.19770960606
出版商:WILEY‐VCH Verlag
年代:1977
数据来源: WILEY
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6. |
Vinylcopper(I) compounds: Part III: Direct conversion of 1‐alkenylcuprates into stereospecifically substituted 1‐halogeno‐1‐alkenes |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 96,
Issue 6,
1977,
Page 168-171
H. Westmijze,
J. Meijer,
P. Vermeer,
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摘要:
AbstractHalogenation of vinylcopper(I) compounds [RR′CCHCu(Br or R)]MgX, prepared stereospecifically bycis‐addition of [RCuBr]MgX or [R2Cu]MgX to 1‐alkynes R′‐C≡CH in tetrahydrofuran, with one of the halogenating reagentsN‐chlorosuccinimide,N‐bromosuccinimide, BrCN, ICN or I2, leads in high yields to the corresponding 1‐halogeno‐1‐alkenes RR′CCHX (X = Cl, Br or I). The introduction of the halogen atom occurs with retention of configura
ISSN:0165-0513
DOI:10.1002/recl.19770960607
出版商:WILEY‐VCH Verlag
年代:1977
数据来源: WILEY
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7. |
Total synthesis of methylt‐5,c‐8,c‐11,c‐14‐ andc‐5,c‐8,c‐11,t‐14‐eicosatetraenoate and oft‐2,c‐5,c‐8,c‐11,c‐14‐eicosapentaenoic acid |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 96,
Issue 6,
1977,
Page 172-175
G.J.N. Egmond,
H.J.J. Pabon,
D.A. van Dorp,
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摘要:
AbstractOn the basis oftrans‐2‐hexene‐1,6‐diol andtrans‐2‐octenol, both obtained by trans reduction of their acetylenic precursors with sodium in liquid ammonia,trans‐5‐eicosene‐8,1 1,14‐triynoic acid andtrans‐ 14‐eicosene‐5,8,11‐triynoic acid were built up by classical methods. Partial hydrogenation and esterification afforded the desired eicosatetraenoates. In addition, reduction of previously describedtrans‐2‐eicosene‐5,8,11,14‐tetraynoic acid gavet‐2,c
ISSN:0165-0513
DOI:10.1002/recl.19770960608
出版商:WILEY‐VCH Verlag
年代:1977
数据来源: WILEY
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8. |
Vapour phase chemistry of arenes. Part VII: Direct, thermal cyanation of benzene derivatives and pyridine by hydrogen cyanide |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 96,
Issue 6,
1977,
Page 176-178
Kees van Nierop,
Robert Louw,
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摘要:
AbstractBenzene, chlorobenzene or benzonitrile, in the presence of a little C2Cl6or formaldehyde, reacts with HCN at ∼ 480° (30 s) to give the (mono)cyano derivatives. Features, especially isomer distributions for this cyanation closely resemble those for gas‐phase chlorination. By analogy, therefore, a free radical mechanism is advanced involving endothermal hydrogen abstraction by Cl•and/or H•to give aryl radicals, which in turn attack HCN at carbon, displacing hydrogen. Pyridine leads to cyanopyridines (89 % 2‐, 6 % 3‐, 5 % 4‐isomer), the 2‐position being ∼ 3 times as reactive as benzene hydrogens. This supports our view that differences in CH bond strength play a major part, as it is known that 2‐pyridyl is stabilized relative to its 3‐ and 4‐analogues. ICN was found not to be a su
ISSN:0165-0513
DOI:10.1002/recl.19770960609
出版商:WILEY‐VCH Verlag
年代:1977
数据来源: WILEY
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9. |
Electrocyclic opening of benzol [b]thiophene |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 96,
Issue 6,
1977,
Page 178-179
A.E.M. Beyer,
H. Kloosterziel,
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摘要:
AbstractReacting the title compound with lithium dimethylamide and subsequent addition of methyl iodide yieldsE‐β‐(dimethylamino)‐o‐(methylthio
ISSN:0165-0513
DOI:10.1002/recl.19770960610
出版商:WILEY‐VCH Verlag
年代:1977
数据来源: WILEY
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10. |
Trimethylsilylation of lithium 1‐alkyne‐1‐thiolates and formation of 1,3‐dithiole derivatives from 1‐alkynyl disulfides and (trimethylsilylthio)alkynes under nucleophilic conditions: (Preliminary communication) |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 96,
Issue 6,
1977,
Page 179-180
R.S. Sukhai,
J. Meijer,
L. Brandsma,
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ISSN:0165-0513
DOI:10.1002/recl.19770960611
出版商:WILEY‐VCH Verlag
年代:1977
数据来源: WILEY
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