Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Michael D, Dowle"'
Autor:
Simon J F, Macdonald, Geoffrey D E, Clarke, Michael D, Dowle, Lee A, Harrison, Simon T, Hodgson, Graham G A, Inglis, Martin R, Johnson, Prit, Shah, Richard J, Upton, Steven B, Walls
Publikováno v:
The Journal of organic chemistry. 64(14)
A flexible, practical, and stereoselective synthesis of enantiomerically pure
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dd9b13ef74f72d85e684fd8ce230d565
https://pubmed.ncbi.nlm.nih.gov/34237863
https://pubmed.ncbi.nlm.nih.gov/34237863
Publikováno v:
Synthesis. 1979:990-992
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::badc45dbcd70e13d53cda3a5227ae1cc
https://doi.org/10.1055/s-1979-28906
https://doi.org/10.1055/s-1979-28906
Autor:
Michael D. Dowle
Publikováno v:
Chemischer Informationsdienst. 8
Primary thioamides are transformed by diethyl azodicarboxylate and triphenylphosphine into nitriles.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd25e588bcf4b96111380fe148bb2795
https://doi.org/10.1002/chin.197737125
https://doi.org/10.1002/chin.197737125
Publikováno v:
Journal of the Chemical Society, Chemical Communications. :303
Photolysis of hydroxy-, dihydroxy- and amino-bicyclo[n.2.0]alkanones has been used as the key step in the synthesis of naturally occurring lactones including a mosquito pheromone, goniothalamin, argentilactone, and the Streptomyces L-factor, and of a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3aaae9a627d57661e7d9cd55f400dc82
https://doi.org/10.1039/c39890000303
https://doi.org/10.1039/c39890000303
Autor:
Michael D. Dowle
Publikováno v:
Journal of the Chemical Society, Chemical Communications. :220
Primary thioamides are transformed by diethyl azodicarboxylate and triphenylphosphine into nitriles.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fa9d6c105fde1fc0d6e2b74ec1d19b4
https://doi.org/10.1039/c39770000220
https://doi.org/10.1039/c39770000220