Zobrazeno 1 - 10
of 1 453
pro vyhledávání: '"Teruaki Mukaiyama"'
Publikováno v:
ARKIVOC, Vol 2007, Iss 7, Pp 254-264 (2006)
Externí odkaz:
https://doaj.org/article/46887a9448a2457582865ba0fc8c3c05
Publikováno v:
ARKIVOC, Vol 2004, Iss 3, Pp 42-65 (2003)
Externí odkaz:
https://doaj.org/article/ead0695bccec47be8bc63bb867f8882b
Publikováno v:
ARKIVOC, Vol 2001, Iss 10, Pp 58-65 (2001)
Externí odkaz:
https://doaj.org/article/65d0f14ecfa345dea426359c4a1b5d36
Publikováno v:
Helvetica Chimica Acta. 95:1891-1911
Pyridine-3-carboxylic anhydride (3-PCA) was found to function as an efficient coupling reagent for the preparation of carboxylic esters from various carboxylic acids with alcohols under mild conditions by a simple experimental procedure. This novel c
Publikováno v:
Bulletin of the Chemical Society of Japan. 82:381-392
Preparation of alkyl aryl sulfides from alcohols and arenethiols such as 2-sulfanyl-1,3-benzothiazole (BtzSH) is described by a new type of oxidation–reduction condensation using phenyl diphenylpho...
Publikováno v:
Synthetic Communications. 38:3208-3214
(Chloromethylene)dimethylammonium chloride (Vilsmeier reagent) works as an efficient condensation reagent in the formation of carboxylic esters from carboxylic acids and alcohols under mild conditions in a one-pot procedure. Secondary alcohols are co
Autor:
Teruaki Mukaiyama, Setsuo Funasaka
Publikováno v:
Bulletin of the Chemical Society of Japan. 81:148-159
A highly useful method for the preparation of carboxylic esters and carboxamides from various carboxylic acids was established by using a novel condensing reagent, pyridine-3-carboxylic anhydride (...
Publikováno v:
Bulletin of the Chemical Society of Japan. 80:2406-2412
Chiral quaternary ammonium phenoxides were prepared readily from commercially available cinchona alkaloids and employed as novel useful asymmetric organocatalysts. Among these chiral quaternary ammonium phenoxides, a cinchonidine-derived phenoxide th
Publikováno v:
Tetrahedron. 63:6358-6364
A novel method for the preparation of alkyl azides from alcohols by way of oxidation–reduction condensation is described. In this reaction, the sterically-hindered tert-alkyl phosphinites that are prepared from the corresponding alcohols are conver
Publikováno v:
ARKIVOC, Vol 2007, Iss 7, Pp 254-264 (2006)
A convenient method for the Cu(II)-catalyzed O-phenylation of tertiary alcohols with organobismuth(V) compounds under mild conditions is described. Functionalized tertiary alcohols such as α-hydroxy carbonyl compounds were phenylated by using either