Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Ryan M Harrington"'
Autor:
Ryan M Harrington, Arthur de O Lima, Richard Fox-Ivey, Thanh Nguyen, John Laurent, Marcus S Dersch, J Riley Edwards
Publikováno v:
Proceedings of the Institution of Mechanical Engineers, Part F: Journal of Rail and Rapid Transit. 237:137-145
Railroad track inspections conducted in accordance with federal regulations and internal railway operating practices result in significant labor costs and occupy valuable network capacity. These factors, combined with advancements in the field of mac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad55ef7b7cb6b9e2aa648d36e97613bb
https://doi.org/10.1177/09544097221093486
https://doi.org/10.1177/09544097221093486
Publikováno v:
ChemInform. 44
Propargyl xanthates undergo rearrangement to afford intermediary bis(alkylidene)dithiolanones which are trapped by Diels-Alder cycloaddition to yield dithiolones, representing three new carbocycle types such as (II), (VIII), and (X).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba7a46491ffa1b51a69b21b0fbdad0ea
https://doi.org/10.1002/chin.201317107
https://doi.org/10.1002/chin.201317107
Publikováno v:
Heterocycles
Heterocycles, The Japan Institute of Heterocyclic Chemistry, 2012, 86 (2), pp.965-971. ⟨10.3987/com-12-s(n)98⟩
Heterocycles, The Japan Institute of Heterocyclic Chemistry, 2012, 86 (2), pp.965-971. ⟨10.3987/com-12-s(n)98⟩
International audience; Upon heating in chlorobenzene, propargyl xanthates yield the corresponding 4,5-bis(alkylidene)-1,3-dithiolan-2-ones which are trapped by unactivated olefins in an intramolecular Diels-Alder cycloaddition yielding interesting p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4faa6df9e64adc2eeb9c0fd07c7e166
https://hal-polytechnique.archives-ouvertes.fr/hal-00949988/document
https://hal-polytechnique.archives-ouvertes.fr/hal-00949988/document
