Enantioconvergent Synthesis of Functionalized γ-Butyrolactones via (3 + 2)-Annulation [Erratum to document cited in CA162:137454] was written by Goodman, C. Guy;Walker, Morgan M.;Johnson, Jeffrey S.. And the article was included in Journal of the American Chemical Society in 2015.Product Details of 1631733-83-9 The following contents are mentioned in the article:
Some of the catalyst identifiers (A-G) used in the Supporting Information did not match those shown in the paper; the Supporting Information has been updated. The authors were made aware of several relevant publication involving enantioconvergent proline-catalyzed aldol reactions of chiral racemic electrophiles and provide the relevant citation information. This study involved multiple reactions and reactants, such as (S)-5-Isopropyl-2-mesityl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-c][1,4]oxazin-2-ium tetrafluoroborate (cas: 1631733-83-9Product Details of 1631733-83-9).
(S)-5-Isopropyl-2-mesityl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-c][1,4]oxazin-2-ium tetrafluoroborate (cas: 1631733-83-9) belongs to triazole derivatives. The many free lone pairs in triazoles make them useful as coordination compounds, although not typically as haptic ligands. Triazole growth retardants such as uniconazole and paclobutrazol have been known to inhibit the biosynthesis of gibberellins by blocking kaurene oxidase, an P450 enzymeProduct Details of 1631733-83-9
Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics