Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Lee McLaren"'
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :901-910
A series of novel 2-oxo esters with protected alcohols at the 3-, 4-, 5-, 6- and 7-positions has been prepared either via coupling of an aldehyde with an organometallic reagent (Zn, In or Cr) or via a one-carbon homologation of the precursor acid. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9c9aa491b4198f22e107a520f42aa76
https://doi.org/10.1039/a909677i
https://doi.org/10.1039/a909677i
Publikováno v:
Tetrahedron Letters. 40:1069-1072
An efficient synthesis of (S)- and (R)-3-hydroxypiperidin-2-ones from methyl 5-nitro-2-oxopentanoate is described. A one-pot enzyme catalysed hydrolysis of the ester and reduction of the ketone gave enantiopure 2-hydroxy-5-nitropentanoic acids which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::129a7e4fbc43dd5a646864d75fb43bb8
https://doi.org/10.1016/s0040-4039(99)80114-2
https://doi.org/10.1016/s0040-4039(99)80114-2
Publikováno v:
Tetrahedron Letters. 34:5519-5522
A short synthesis of the novel antibiotic aranorosin is described which employs a novel hypervalent iodine-mediated oxidative hydroxylation of a tyrosinal derivative in the key step. A similar procedure was employed to prepare 6′-epiaranorosin, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05ada101fd85f62b655885904b542025
https://doi.org/10.1016/s0040-4039(00)73870-6
https://doi.org/10.1016/s0040-4039(00)73870-6
Publikováno v:
ChemInform. 24
A short synthesis of the novel antibiotic aranorosin is described which employs a novel hypervalent iodine-mediated oxidative hydroxylation of a tyrosinal derivative in the key step. A similar procedure was employed to prepare 6′-epiaranorosin, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::988110c199169d740a4296ca139564ea
https://doi.org/10.1002/chin.199352292
https://doi.org/10.1002/chin.199352292
Publikováno v:
ChemInform. 26
Oxidation of para-substituted phenols with [bis(trifluoroacetoxy)iodo] benzene (BTIB) in aqueous acetonitrile at 0 °C gives p-quinols in moderate to good yields; higher yields are obtained when tripropylsilyl ethers of phenols are used.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34652b5fa7cf29f8951ff6582a419679
https://doi.org/10.1002/chin.199501118
https://doi.org/10.1002/chin.199501118
Publikováno v:
ChemInform. 30
An efficient synthesis of (S)- and (R)-3-hydroxypiperidin-2-ones from methyl 5-nitro-2-oxopentanoate is described. A one-pot enzyme catalysed hydrolysis of the ester and reduction of the ketone gave enantiopure 2-hydroxy-5-nitropentanoic acids which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b35448967085d3fec41885a718897497
https://doi.org/10.1002/chin.199920114
https://doi.org/10.1002/chin.199920114
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45bb24d932b1cf38c69fdb90e84a1730
https://doi.org/10.1002/chin.200026072
https://doi.org/10.1002/chin.200026072
Autor:
Mara Lee McLaren
Publikováno v:
Linear Algebra and its Applications. 127:601-616
This paper shows how the likelihood ratio for testing the equality of two variance-covariance matrices decomposes asymptotically into two separate tests, one for equality of the latent roots or eigenvalues, and the other for equality of the eigenvect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::912c8f17166638a8d57aec3b0de5a2ad
https://doi.org/10.1016/0024-3795(90)90364-i
https://doi.org/10.1016/0024-3795(90)90364-i
Publikováno v:
Synlett. 1992:201-203
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3fba41dd46d77fa147e0030f37a9c97
https://doi.org/10.1055/s-1992-21313
https://doi.org/10.1055/s-1992-21313
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :1385
A short synthesis of the novel antibiotic aranorosin in chiral form is described which employs (i) a novel hypervalent iodine-mediated oxidative hydroxylation of a tyrosinal derivative and (ii) a stereocontrolled cis-bisepoxidation in the key steps.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff84b44ca09b405f3f7e5f24ac27eb3e
https://doi.org/10.1039/p19960001385
https://doi.org/10.1039/p19960001385