Zobrazeno 1 - 8
of 8
pro vyhledávání: '"W. P. England"'
Publikováno v:
Journal of the American Chemical Society. 114:2635-2643
d,l- and meso-2,2'-bis[1-methylene-1,2,3,4-tetrahydronaphthalenes] 8 and 9 were synthesized, and the activation energy parameters for their unimolecular [3,3] sigmatropic rearrangement to 1,2-bis(3,4-dihydro-1-naphthalenyl)ethane (13) were determined
Publikováno v:
Tetrahedron Letters. 31:6843-6846
The X-ray crystal structure of 3-oxabicyclo[5.3.1]deca-1(10),7(8)-(ZZ)-diene-10-carboxylic acid, a highly strained bridgehead diene, is reported.
Publikováno v:
Tetrahedron Letters. 29:407-410
1,2-Cyclooctadienes are proposed as intermediates in the intramolecular ene cyclization of acyclic 1,7-octenyne derivatives.
Publikováno v:
Tetrahedron Letters. 28:5623-5626
Sequential dichlorocyclopropanation and ethoxide induced lactone cleavage of bridgehead enol lactones affords a stereocontrolled synthesis of 2-chlorocycloheptenones.
Publikováno v:
Journal of the American Chemical Society. 110:860-864
Cycloaddition intramoleculaire de divers esters dienyne comportant pour la plupart une fonction ether entre les parties diene et dienophile. Effet de la position de l'atome d'oxygene et de la longueur de chaine sur la cinetique. Obtention de derives
Publikováno v:
ChemInform. 19
Sequential dichlorocyclopropanation and ethoxide induced lactone cleavage of bridgehead enol lactones affords a stereocontrolled synthesis of 2-chlorocycloheptenones.
Publikováno v:
ChemInform. 19
1,2-Cyclooctadienes are proposed as intermediates in the intramolecular ene cyclization of acyclic 1,7-octenyne derivatives.
Publikováno v:
ChemInform. 19
Cycloaddition intramoleculaire de divers esters dienyne comportant pour la plupart une fonction ether entre les parties diene et dienophile. Effet de la position de l'atome d'oxygene et de la longueur de chaine sur la cinetique. Obtention de derives