Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Toni Moragas Solá"'
Autor:
Ian Churcher, Toni Moragas Solá, Heather Hobbs, Leonid Sasraku-Neequaye, Robert A. Stockman, David MacPherson, Caroline Roe
Publikováno v:
ChemInform. 42
The synthetic utility of S-mesitylsulfinimines for the synthesis of chiral amines and aziridines was examined through their reactions with Grignard reagents, with the ylides derived from trimethylsulfonium iodide and S-allyl-tetrahydrothiophenium bro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6a74de8add9b1d21229d2e69a2a9145
https://doi.org/10.1002/chin.201146021
https://doi.org/10.1002/chin.201146021
Publikováno v:
Organicbiomolecular chemistry. 9(14)
Stereoselective synthesis of 2,3-di- and 2,2′,3-tri-substituted aziridines in good yields and excellent diastereoselectivities are achieved through aza-Darzens reactions of a range of tert-butanesulfinyl aldimines and ketimines with ethyl bromoacet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41996c7db598279c0c348316e66016e8
https://pubmed.ncbi.nlm.nih.gov/21643589
https://pubmed.ncbi.nlm.nih.gov/21643589
Autor:
Leonid Sasraku-Neequaye, Ian Churcher, Toni Moragas Solá, Heather Hobbs, Caroline Roe, David MacPherson, Robert A. Stockman
Publikováno v:
Chemical Communications. 47:7491
The synthetic utility of S-mesitylsulfinimines for the synthesis of chiral amines and aziridines was examined through their reactions with Grignard reagents, with the ylides derived from trimethylsulfonium iodide and S-allyl-tetrahydrothiophenium bro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7ebff1f1e9e71b8b2085474a621eee2
https://doi.org/10.1039/c1cc11870f
https://doi.org/10.1039/c1cc11870f
Publikováno v:
Acta Crystallographica Section E: Structure Reports
Acta Crystallographica Section E, Vol 66, Iss 12, Pp o3335-o3335 (2010)
Acta Crystallographica Section E, Vol 66, Iss 12, Pp o3335-o3335 (2010)
The reaction of a sulfur ylide with a chiral non-racemic sulfinyl imine afforded the desired aziridine in excellent yield and subsequent oxidation of the sulfinyl moiety dissolved in anhydrous dichloromethane using a 75% aqueous solution of 3-chlorop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9df6aada36b38953a9c640f349a9cac8
https://doi.org/10.1107/s1600536810048816
https://doi.org/10.1107/s1600536810048816
Publikováno v:
Acta Crystallographica Section E, Vol 66, Iss 12, Pp o3335-o3335 (2010)
The reaction of a sulfur ylide with a chiral non-racemic sulfinyl imine afforded the desired aziridine in excellent yield and subsequent oxidation of the sulfinyl moiety dissolved in anhydrous dichloromethane using a 75% aqueous solution of 3-chlorop
Externí odkaz:
https://doaj.org/article/ed6e04c50a334225985db9a240678003