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pro vyhledávání: '"V. Guagnano"'
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Publikováno v:
Canadian Journal of Chemistry. 79:1606-1616
Chemical transformation of nitroso acetals derived from tandem [4 + 2]/[3 + 2] cycloadditions of nitroalkenes have been investigated. New reduction methods were surveyed in an attempt to supplant the use of hydrogen and Raney nickel. Homogeneous cata
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8525b0a3437c21a5cd7e3640350d146c
https://doi.org/10.1139/v01-132
https://doi.org/10.1139/v01-132
Publikováno v:
The Journal of Organic Chemistry. 62:4610-4628
A new variant of the tandem inter [4 + 2]/intra [3 + 2] cycloaddition of nitroalkenes is described in detail. The scope and limitations of the bridged mode tandem cycloaddition in which the diene a...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd6a45ca6fab3662e42ebfd684b5fbdf
https://doi.org/10.1021/jo970686m
https://doi.org/10.1021/jo970686m
Publikováno v:
ChemInform. 23
3-Nitro-5,6-dihydro-4H-pyran reacts with organoaluminum compounds and, after hydrolysis with 3 N HCl;, gives aldehydes arising from a formal carbonylation of the alane.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bfdb8b88d48760c8f02fbb5e42b81cb3
https://doi.org/10.1002/chin.199246107
https://doi.org/10.1002/chin.199246107
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f217b93a2097055dae92d50549eafdd
https://doi.org/10.1002/chin.199320127
https://doi.org/10.1002/chin.199320127
Publikováno v:
ChemInform. 25
3-Nitro-5,6-dihydro-4H-pyran reacts with organoalanes and gives 1, 4 addition products. In suitable hydrolysis conditions, the reaction results in the formation of aldehydes that are C 1 -homologues of the chain transferred by the alane.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6fef85f1f8748c29adfd40ac853a0679
https://doi.org/10.1002/chin.199423096
https://doi.org/10.1002/chin.199423096
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::694257c19d3050bea7b48bd52a8052ad
https://doi.org/10.1002/chin.199530031
https://doi.org/10.1002/chin.199530031
Publikováno v:
ChemInform. 27
3-Nitro-5,6-dihydro-4H-pyran reacts with primary aliphatic and benzylic Grignard reagents and, in suitable hydrolysis conditions, gives the corresponding 2-alkyltetrahydropyran-3-ones in satisfactory yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f153cd04c20b4b69abc423b4a98aeac
https://doi.org/10.1002/chin.199615155
https://doi.org/10.1002/chin.199615155
Publikováno v:
ChemInform. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4534eaefa3178297b61e2d8583a935aa
https://doi.org/10.1002/chin.199750049
https://doi.org/10.1002/chin.199750049
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f6513c089569b15100198294a068d94
https://doi.org/10.1002/chin.199827155
https://doi.org/10.1002/chin.199827155