Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Yuta Saga"'
Publikováno v:
Inorganics, Vol 5, Iss 1, p 5 (2017)
P-Fluorous phosphine (R2PRf), in which the perfluoroalkyl group is directly bonded to the phosphorus atom, is a promising ligand because it has a hybrid functionality, i.e., electron-poor and fluorous ligands. However, examples of P-fluorous phosphin
Externí odkaz:
https://doaj.org/article/b388d4a8847b41139952bc4afc408cdc
Autor:
Li-Biao Han, Shu Kobayashi, Shun-ya Onozawa, Jian-Qiu Zhang, Norihisa Fukaya, Jingjing Ye, Kazuhiko Sato, Yuta Saga
Publikováno v:
Organometallics. 39:2682-2694
The preparation, application, and reaction mechanism of sodium phosphide R2PNa and other alkali metal phosphides R2PM (M = Li and K) have been studied. R2PNa could be prepared, accurately and selec...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9768be7838f947767715b2d89118438a
https://doi.org/10.1021/acs.organomet.0c00295
https://doi.org/10.1021/acs.organomet.0c00295
Autor:
Li-Biao Han, Shu Kobayashi, Kazuhiko Sato, Chunya Li, Yuta Saga, Norihisa Fukaya, Shun-ya Onozawa
Publikováno v:
The Journal of organic chemistry. 85(22)
A "wet" process and two "dry" processes for converting phosphonate esters to phosphonic acids catalyzed by a Bronsted acid have been developed. Thus, in the presence of water, a range of alkyl-, alkenyl-, and aryl-substituted phosphonates can be gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::445bee2e6421e7446185d819f5b675cd
https://pubmed.ncbi.nlm.nih.gov/32434328
https://pubmed.ncbi.nlm.nih.gov/32434328
Publikováno v:
The Journal of Organic Chemistry. 83:8743-8749
Radical hydrophosphorylation of aliphatic terminal alkynes with H-phosphine oxides can produce the corresponding anti-Markovnikov alkenylphosphorus adducts in moderate yields. This method is a cleaner approach for the preparation of the corresponding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e86107dd84522b3465afe2a48ea91af3
https://doi.org/10.1021/acs.joc.8b01042
https://doi.org/10.1021/acs.joc.8b01042
Publikováno v:
Tetrahedron. 73:7085-7093
Trimethyl phosphine was used as an efficient catalyst for the addition of P(O)-H compounds to electron-deficient alkenes. The addition reactions were generally conducted using a catalytic amount of Me3P under mild reaction conditions. Both 1 to 1 and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4f98e22e1579020aa3fd0aad652a6aa
https://doi.org/10.1016/j.tet.2017.10.070
https://doi.org/10.1016/j.tet.2017.10.070
Publikováno v:
Tetrahedron: Asymmetry. 28:84-89
A variety of P -stereogenic organophosphorus compounds can be readily prepared by stereoretentive addition. The PMe 3 -catalyzed addition of optically active (−)MenthylO(Ph)P(O)H compounds to electron deficient alkenes occur stereospecifically, to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65d17b7662cca18973ad69260cd0a09d
https://doi.org/10.1016/j.tetasy.2016.11.005
https://doi.org/10.1016/j.tetasy.2016.11.005
Publikováno v:
Green Chemistry. 19:1502-1506
An air-induced double addition of diphenyl phosphine oxide to various alkynes is reported. This reaction can proceed efficiently under metal- and solvent-free conditions, and is a clean and practically useful method for the preparation of the valuabl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35457ca2c4af3bb1306080d754a96020
https://doi.org/10.1039/c6gc03240k
https://doi.org/10.1039/c6gc03240k
Publikováno v:
The Journal of organic chemistry. 83(15)
Radical hydrophosphorylation of aliphatic terminal alkynes with H-phosphine oxides can produce the corresponding anti-Markovnikov alkenylphosphorus adducts in moderate yields. This method is a cleaner approach for the preparation of the corresponding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::49077675e1762655e6458c6ee1186d67
https://pubmed.ncbi.nlm.nih.gov/29927246
https://pubmed.ncbi.nlm.nih.gov/29927246
Publikováno v:
Tetrahedron Letters. 56:5303-5305
A convenient and versatile method was developed for the preparation of 1,2-bisphosphorylethanes. Thus, in the presence of a catalytic amount of trimethylphosphine, a variety of >P(O)H compounds efficiently add to vinylphosphoryl compounds to produce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87501e0e853a4d65dddf0fc92d1be18f
https://doi.org/10.1016/j.tetlet.2015.07.077
https://doi.org/10.1016/j.tetlet.2015.07.077
Publikováno v:
RSC Advances. 5:71544-71546
Chloroform-based Atherton–Todd-type reactions of alcohols and thiols with secondary phosphine oxides, generating phosphinothioates and phosphinates, respectively, are described. Various valuable phosphinothioates and phosphinates including those wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76531af1f427ce7736511aef4b2ec920
https://doi.org/10.1039/c5ra16015d
https://doi.org/10.1039/c5ra16015d