WebAug 13, 2006 · An efficient, scaleable synthesis approach towards the spirocyclic oxindole analogue 1’-(tert-butoxycarbonyl)-2-oxospiro[indoline-3,4’-piperidine]-5-carboxylic acid (1) is described. The key steps are dianion alkylation and cyclization of ethyl 2- oxindoline-5-carboxylate (4) and demethylation of the resulting spirocyclic oxindole ethyl 1’-methyl-2 … WebJan 1, 1975 · Alkylation of the chrysin dianion 267 The benzylation of chrysin 1. With benzyl chloride in dioxan. A suspension of the disodium salt of 1 (0-0025 mole) in dioxan …
Synthesis and Ring-Opening Metathesis Polymerization of a …
WebDec 19, 2014 · Syntheses of 2,5- and 3,5-disubstituted 7-aminoindoles are illustrated. Additionally, dianion alkylation of the allylic nitrile is demonstrated to furnish, after cyclization, 5,6-disubstituted 7-aminoindoles to further exemplify this scalable and high-yielding method. WebDec 24, 1993 · A series of C-9 beta-substituted artemisinin analogs (2-21) were synthesized via dianion alkylation of the total synthetic intermediate 57 followed by subsequent ozonolysis/acidification, or by alkylation of the enolate derived from (+)-9-desmethylartemisinin, 2. Inactive acyclic analogs 22 and 23 w … software components of client server system
Study of the lithiated phenylacetonitrile monoanions and …
WebDephosphonylation of α-fully substituted β-keto phosphonates with LiAlH4; regioselective alkylation of ketones employing phosphonate as a temporary activating group. Tetrahedron Letters 1997 , 38 (26) , 4567-4570. Webdianion I and II. You should read the abstract and look at Scheme 1 (p. 3082) and Table 4 (p. 3086). ... Enamines normally react with methyl iodide to give two products: one arising from alkylation at nitrogen and the second arising from alkylation at carbon. For example, Heating the mixture of C-alkylation and N-alkylation products gives only ... WebFeb 7, 2008 · Particularly, nitromethane (10) can be regarded as a d 1,d 1 multiple coupling reagent corresponding to a carbonyl dianion synthon . Scheme 4. ... The introduction of a further carbon framework containing the second hydroxy group is realized by a regioselective alkylation of ketone 55 with chloroalkane 56. software.com pc