Zobrazeno 1 - 10
of 10
pro vyhledávání: '"I. P. Kupchik"'
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fde865574a315a53453245e8a49d6d55
https://doi.org/10.1002/chin.199040148
https://doi.org/10.1002/chin.199040148
Publikováno v:
Chemistry of Heterocyclic Compounds. 24:1328-1330
Derivatives of cyclopenta[b]tetrahydrofurans are formed as a result of the iodocyclization of cis-1-R-2-allylcyclopentan-1-ols. The iodocyclization reaction of unsaturated alcohols is described by a kinetic equation of the second order (the first ord
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97f670fe3fd8199255e802e8e9161ec0
https://doi.org/10.1007/bf00486671
https://doi.org/10.1007/bf00486671
Publikováno v:
Chemistry of Heterocyclic Compounds. 17:24-26
The corresponding tetrahydrofuran derivatives were obtained by iodination of δ, ɛ- unsaturated alcohols containing substituents attached to the α-carbon atom. The effect of substituents on the stereochemistry of the products and the rate of iodina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d4041982b2e2f4bcc4029996069f134
https://doi.org/10.1007/bf00507083
https://doi.org/10.1007/bf00507083
Publikováno v:
Chemistry of Heterocyclic Compounds. 21:135-137
Iodination of 2-allylcyclohexanol and its 1-methyl and 1-phenyl derivatives gives the corresponding 2-(iodomethyl)octahydrobenzofurans. These are reduced by to the stereoisomeric 2-methyloctahydrobenzofurans. The rate of iodination of 2-allylcyclohex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70fb87b65117750d47115fdc3620ead6
https://doi.org/10.1007/bf00504193
https://doi.org/10.1007/bf00504193
Publikováno v:
Chemischer Informationsdienst. 12
The corresponding tetrahydrofuran derivatives were obtained by iodination of δ, ɛ- unsaturated alcohols containing substituents attached to the α-carbon atom. The effect of substituents on the stereochemistry of the products and the rate of iodina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::969f79339426654ad1c905006b771399
https://doi.org/10.1002/chin.198124220
https://doi.org/10.1002/chin.198124220
Publikováno v:
Chemischer Informationsdienst. 13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f13093570709669886a88dda0268da64
https://doi.org/10.1002/chin.198226180
https://doi.org/10.1002/chin.198226180
Publikováno v:
ChemInform. 20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59302483720f5f732c9380b2a224d212
https://doi.org/10.1002/chin.198930160
https://doi.org/10.1002/chin.198930160
Publikováno v:
Chemischer Informationsdienst. 16
Iodination of 2-allylcyclohexanol and its 1-methyl and 1-phenyl derivatives gives the corresponding 2-(iodomethyl)octahydrobenzofurans. These are reduced by to the stereoisomeric 2-methyloctahydrobenzofurans. The rate of iodination of 2-allylcyclohex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d5e71d0c942917c36959d20a6fd1434
https://doi.org/10.1002/chin.198529181
https://doi.org/10.1002/chin.198529181
Publikováno v:
ChemInform. 20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3bc34cfd2cd7f3f7be46a18947b56616
https://doi.org/10.1002/chin.198947241
https://doi.org/10.1002/chin.198947241
Publikováno v:
ChemInform. 20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf7a6a7908c104251d03ca442ded0fe7
https://doi.org/10.1002/chin.198924076
https://doi.org/10.1002/chin.198924076