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1. |
Addition of phenols and alcohols to ethoxyethyne Formation of orthoacetates or ketene acetals |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 94,
Issue 9‐10,
1975,
Page 209-210
R.J. Broekema,
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摘要:
AbstractAddition of phenols and of alcohols to ethoxyethyne, under the influence of mercury(II) acetate and zinc chloride respectively, affords orthoacetates. Ketene acetals can be isolated with sterically hindered phenols.
ISSN:0165-0513
DOI:10.1002/recl.19750940902
出版商:WILEY‐VCH Verlag
年代:1975
数据来源: WILEY
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2. |
Stereoselectivity and proton binding in copper(II) complexes of aspartic acid, glutamic acid and someN‐methyl orN‐benzylhistidine derivatives |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 94,
Issue 9‐10,
1975,
Page 210-215
J.H. Ritsma,
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摘要:
AbstractStability constants and stereoselective effects are measured for copper(II) complexes with aspartate (asp), glutamate (glut), histidinate (his) and someN‐alkylhistidinate derivatives:N‐methyl‐ (mhis),N,N‐dimethyl‐ (dimhis) andN‐benzylhistidinate (bhis). For the dicarboxylic amino acids the predominant species in solution are CuA, CuHA and CuA2*; for histidine and its derivatives:CuA, CuHA, CuA2and CuHA2. By comparison of competition constants (vide infra) it is found that the ligand is boundviaits glycine‐locus in all complexes CuHA. For complexes CuHA2, the mono‐protonated ligand, HA, is also bound to copper by its glycine‐locus if A = his and bhis, and mainly so if A = mhis, but, if A = dimhis, HA, possibly, is monodentate and bound to copper by its imidazole group. No stereoselective effects are found in complexes CuA2for A = asp, glut, his and mhis; for A = dimhis a significant positive effect (i.e.in favour of themesocomplex Cu(DA)(LA)) is found, in contrast to the case for A = bhis. In the protonated copper complexes CuHA2, small negative effects are found for A = his, mhis and bhis, but
ISSN:0165-0513
DOI:10.1002/recl.19750940903
出版商:WILEY‐VCH Verlag
年代:1975
数据来源: WILEY
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3. |
The reactions between 1′,3′,3′‐trimethylspiro[2H‐1‐benzopyran‐2,2′‐indolines] and 1,1‐bis[4‐(dimethylamino)phenyl]ethylene; products and mechanism |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 94,
Issue 9‐10,
1975,
Page 215-218
D.J. Zwanenburg,
Th. A. M. M. Maas,
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摘要:
AbstractThe reaction between 1′,3′,3′‐trimethylspiro[2H‐1‐benzopyran‐2,2′‐indoline] and its derivatives (3a‐e) and 1,1‐bis[4‐(dimethylamino)phenyl]ethylene (“Michler's ethylene”) (4) were studied. Depending on the reaction time, the isomeric products 2,2‐bis[4‐(dimethylamino)phenyl]‐4‐{2‐methylidene‐1,3,3‐trimethylindoline}chromans (7a‐e) or 1′,3′,3′‐trimethyl‐4‐{2,2‐bis[4‐(dimethyl‐amino)phenyl]vinyl}‐spiro[chroman‐2,2′‐indolines](8a‐d) were obtained. With deuterium labelled “Michler's ethylene” and deuterated solvents the mechanism of this reaction was confirmed. Reaction of the 2,2‐bis[4‐(dimethylamino)phenyl]‐2H‐chromenes10c,dand 1,3,3‐trimethyl‐2‐methylene‐indoline (9) furnished the dihydrospiropyrans8c,d. Chromene10cand 1,1‐bis(p‐methoxyphenyl)‐ethylene gave 2.2‐bis(4‐methoxyphenyl)‐4‐ [2,2‐bis[4‐(dim
ISSN:0165-0513
DOI:10.1002/recl.19750940904
出版商:WILEY‐VCH Verlag
年代:1975
数据来源: WILEY
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4. |
Structure analysis of the reaction products of 1′,3′,3′‐trimethylspiro[2H‐1‐benzopyran‐2,2′‐indolines] with 1,1‐bis[4‐(dimethylamino)phenyl]ethylene and related compounds |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 94,
Issue 9‐10,
1975,
Page 218-220
H.M. van Den Bogaert,
D.J. Zwanenburg,
Th. A. M. M. Maas,
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摘要:
AbstractReaction of 1′,3′,3′‐trimethylspiro[2H‐1‐benzopyran‐2,2′‐indolines] with 1,1‐bis[4‐(dimethylamino)phenyl]ethylene can give two types of isomeric products, 2,2‐bis[4‐(dimethylamino)‐phenyl]‐4‐{2‐methylidene‐1,3,3‐trimethylindoline}chromans (2a–e) and 1′,3′,3′‐trimethyl‐4‐{2,2‐bis[4‐(dimethylamino)phenyl]vinyl}‐spiro[chroman‐2,2′‐indolines](3a–d).These products and related compounds have been analysed by spectroscopic methods. The conformation of the dihydropyran ring and the chemical
ISSN:0165-0513
DOI:10.1002/recl.19750940905
出版商:WILEY‐VCH Verlag
年代:1975
数据来源: WILEY
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5. |
(2 + 2)‐Cycloaddition of 9,10‐phenanthrenequinone to alkyl‐substituted aminoacetylenes. Isomerisation of the adductsviaphotochemical γ‐hydrogen‐abstraction andviabase‐catalysis. Preparation of some phenanthro(9,10‐b]furan‐2‐one derivatives |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 94,
Issue 9‐10,
1975,
Page 220-222
A. Mosterd,
H.J.T. Bos,
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摘要:
AbstractPhenanthrenequinone (1) reacts with 1‐dialkylamino‐1‐alkynes2via(2 + 2)‐cyclo‐addition to γ‐oxo‐α,β‐unsatutrated amides3Eof the quinone methide type.These adducts isomerise under the influence of base to α,β‐unsaturated hydroxyamides4. Irradiation of the adducts3Ein benzene affords the same α,β‐unsaturated hydroxyamides4viaintramolecular hydrogen‐abstraction.Treatment of3Ewith boron trifluoride gives 3‐alkyl‐3‐dialkylamino‐2,3‐dihydrophenanthro[9,10‐b]furan‐2‐ones6in good yields. With hydrochloric acid in acetic acid, the unsaturated hydroxyamides 4 afford 3‐alkylidene‐2,3‐dihydrophenanthro[9,10‐b]furan‐2‐ones 7. Similar reactions have been
ISSN:0165-0513
DOI:10.1002/recl.19750940906
出版商:WILEY‐VCH Verlag
年代:1975
数据来源: WILEY
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6. |
Masthead |
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Recueil des Travaux Chimiques des Pays‐Bas,
Volume 94,
Issue 9‐10,
1975,
Page -
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ISSN:0165-0513
DOI:10.1002/recl.19750940901
出版商:WILEY‐VCH Verlag
年代:1975
数据来源: WILEY
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