Visualitza per autoria "7d610132-16f7-4c90-bd81-6be0d06cb665"
Ara mostrant els elements 1-3 d 3
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Highly stereoselective epoxidation of O-protected 3-hydroxy-1-nitroalkenes
Jain, Amit; Rodríguez, Santiago; López Martín, Irakusne; González, Florenci Elsevier (2009)[No abstract available] -
Stereoisomerization of α-hydroxy-β-sulfenyl-α,β-dimethyl naphthoquinones controlled by nonbonded sulfur–oxygen interactions
Latorre, Antonio; Rodríguez, Santiago; Jain, Amit; González, Florenci; Mata Martínez, Jose A Elsevier (2013-03)The anti α-hydroxy-β-sulfenyl-α,β-dimethyl naphthoquinones isomerize in basic media into syn/anti mixtures of isomers, giving the syn isomer as the major product. Conversely, anti α-hydroxy-β-alkoxy-α,β-dimethyl naphthoquinones ... -
Stereoisomerization of β-Hydroxy-α-sulfenyl-γ-butyrolactones Controlled by Two Concomitant 1,4-Type Nonbonded Sulfur−Oxygen Interactions As Analyzed by X-ray Crystallography
González, Florenci; Jain, Amit; Rodríguez, Santiago; Sáez, José A.; Vicent Barrera, Cristian; Peris, Gabriel American Chemical Society (2010)We have synthesized nine β-hydroxy-α-sulfenyl-γ-butyrolactones having different substituents. The syn-anti or syn-syn lactones (or any mixture of both) invariably isomerized into syn-anti/syn-syn lactones in a ratio of ...