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ASYMMETRIC EPOXIDATION OF trans-β-METHYLSTYRENE AND 1-PHENYLCYCLOHEXENE USING A D-FRUCTOSE-DERIVED KETONE: (R,R)-trans-β-METHYLSTYRENE OXIDE AND (R,R)-1-PHENYLCYCLOHEXENE OXIDE ((Oxirane, 2-methyl-3-phenyl-, (2R,3R)- and 7-Oxabicyclo[4.1.0]heptane,1-phenyl-))

Reactions · Organic Syntheses

ASYMMETRIC EPOXIDATION OF trans-β-METHYLSTYRENE AND 1-PHENYLCYCLOHEXENE USING A D-FRUCTOSE-DERIVED KETONE: (R,R)-trans-β-METHYLSTYRENE OXIDE AND (R,R)-1-PHENYLCYCLOHEXENE OXIDE ((Oxirane, 2-methyl-3-phenyl-, (2R,3R)- and 7-Oxabicyclo[4.1.0]heptane,1-phenyl-))

Reaction equation for ASYMMETRIC EPOXIDATION OF trans-β-METHYLSTYRENE AND 1-PHENYLCYCLOHEXENE USING A D-FRUCTOSE-DERIVED KETONE: (R,R)-trans-β-METHYLSTYRENE OXIDE AND (R,R)-1-PHENYLCYCLOHEXENE OXIDE ((Oxirane, 2-methyl-3-phenyl-, (2R,3R)- and 7-Oxabicyclo[4.1.0]heptane,1-phenyl-))

Preparation of (Oxirane, 2-methyl-3-phenyl-, (2R,3R)- and 7-Oxabicyclo[4.1.0]heptane,1-phenyl-). Submitted by Zhi-Xian Wang, Lianhe Shu, Michael Frohn, Yong Tu, and Yian Shi1. DOI: 10.15227/orgsyn.080.0009.

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