Results 141 to 150 of about 42,788 (184)
Some of the next articles are maybe not open access.
Polycarbocyclic Bridged Ring Compounds
1991Publisher Summary This chapter reviews significant advances in the synthesis and chemistry of polycarbocyclic bridged ring compounds. This class of compounds frequently possesses rigid structures whose carbocyclic frameworks contain varying degrees of steric strain and in recent years, highly region- and stereo selective methods have been developed ...
openaire +1 more source
Journal of the Chemical Society, Chemical Communications, 1986
Various N-vinyl- and N-allyl-amides of 2-iodobenzoic acid undergo catalytic cyclisation in the presence of tetraethylammonium chloride and a palladium acetate-based catalyst system to generate a range of synthetically useful structural features including tetrasubstituted carbon centres, and spiro- and bridged-ring compounds, and in which 5-exo-trig ...
Ronald Grigg +3 more
openaire +1 more source
Various N-vinyl- and N-allyl-amides of 2-iodobenzoic acid undergo catalytic cyclisation in the presence of tetraethylammonium chloride and a palladium acetate-based catalyst system to generate a range of synthetically useful structural features including tetrasubstituted carbon centres, and spiro- and bridged-ring compounds, and in which 5-exo-trig ...
Ronald Grigg +3 more
openaire +1 more source
Journal of the Chemical Society, Perkin Transactions 1, 1979
2, 3, 4, 5-Tetrahydro-1, 4-dimethyl-5-oxo-1-benzazepine has been obtained by methylation (Mel) of 2, 3, 4, 5-tetrahydro-5-oxo-1H-1-benzazepine using lithium di-isopropylamide, but a similar attempted alkylation reaction with 1, 2-di-iodoethane was unsuccessful.
Mary Lennon, George R. Proctor
openaire +1 more source
2, 3, 4, 5-Tetrahydro-1, 4-dimethyl-5-oxo-1-benzazepine has been obtained by methylation (Mel) of 2, 3, 4, 5-tetrahydro-5-oxo-1H-1-benzazepine using lithium di-isopropylamide, but a similar attempted alkylation reaction with 1, 2-di-iodoethane was unsuccessful.
Mary Lennon, George R. Proctor
openaire +1 more source
ChemInform, 1987
AbstractThe iodine‐substituted enamides (I), (IV), (VI), and (IX) are cyclized, yielding the compounds (II), (V), (VII), (VIII), and (X).
R. GRIGG +3 more
openaire +1 more source
AbstractThe iodine‐substituted enamides (I), (IV), (VI), and (IX) are cyclized, yielding the compounds (II), (V), (VII), (VIII), and (X).
R. GRIGG +3 more
openaire +1 more source
Chemischer Informationsdienst, 1980
AbstractAusgehend von dem Methoxybenzaldehyd (I) und dem Diester (II) wird nach angegebener Reaktionsfolge das Benzosuberon (IVb) dargestellt, aus dem über den Alkohol (Va) das Keton (Vc) zugänglich ist.
G. R. PROCTOR, F. J. SMITH
openaire +1 more source
AbstractAusgehend von dem Methoxybenzaldehyd (I) und dem Diester (II) wird nach angegebener Reaktionsfolge das Benzosuberon (IVb) dargestellt, aus dem über den Alkohol (Va) das Keton (Vc) zugänglich ist.
G. R. PROCTOR, F. J. SMITH
openaire +1 more source
Chemischer Informationsdienst, 1979
AbstractDas Piperidinderivat (I) reagiert mit Dihydroresorcin zum Enamin (II), das in den Hydroxyester (III) übergeführt wird.
M. LENNON, G. R. PROCTOR
openaire +1 more source
AbstractDas Piperidinderivat (I) reagiert mit Dihydroresorcin zum Enamin (II), das in den Hydroxyester (III) übergeführt wird.
M. LENNON, G. R. PROCTOR
openaire +1 more source
J. Chem. Soc., Perkin Trans. 1, 1976
The 4-arylcyclohex-3-enecarboxylic acids (4a—d), prepared through a modified Diels–Alder reaction, have been converted via the corresponding diazomethyl ketones (5a—d) into cyclopropyl ketones (6a—d) and the 2-aryl-6-oxobicyclo[3.2.1]oct-2-ene derivatives (7a—d), by oxo-carbenoid addition and boron trifluoride–ether-catalysed cyclisation, respectively,
Usha R. Ghatak +3 more
openaire +1 more source
The 4-arylcyclohex-3-enecarboxylic acids (4a—d), prepared through a modified Diels–Alder reaction, have been converted via the corresponding diazomethyl ketones (5a—d) into cyclopropyl ketones (6a—d) and the 2-aryl-6-oxobicyclo[3.2.1]oct-2-ene derivatives (7a—d), by oxo-carbenoid addition and boron trifluoride–ether-catalysed cyclisation, respectively,
Usha R. Ghatak +3 more
openaire +1 more source
Chemischer Informationsdienst, 1976
AbstractAus den Phenyl‐methyl‐ketonen (I) und dem Grignard‐Reagenz (II) werden die ungesättigten Alkohole (III) erzeugt und mit den Acrylaten (IV) zu den Phenylcyclohexencarbonsäureestern (V) (Ausbeuteangaben in g) umgesetzt; die daraus erhaltenen freien Säuren (VI) werden in die Diazoketone (VII) übergeführt, deren photoinduzierte Zersetzung in ...
U. R. GHATAK +3 more
openaire +1 more source
AbstractAus den Phenyl‐methyl‐ketonen (I) und dem Grignard‐Reagenz (II) werden die ungesättigten Alkohole (III) erzeugt und mit den Acrylaten (IV) zu den Phenylcyclohexencarbonsäureestern (V) (Ausbeuteangaben in g) umgesetzt; die daraus erhaltenen freien Säuren (VI) werden in die Diazoketone (VII) übergeführt, deren photoinduzierte Zersetzung in ...
U. R. GHATAK +3 more
openaire +1 more source
Bridged Ring Compounds by Malonic Ester Synthesis
Synthetic Communications, 1977P. A. Verbrugge +3 more
openaire +1 more source
Bridged ring compounds. VIII. 1-Halobicyclo[2.2.-2]octanes
The Journal of Organic Chemistry, 1967Zennosuke Suzuki, Kenichi Morita
openaire +1 more source

