C=C reactions are highly attractive as they are additions, and thus by nature highly atom-economic. Specific topics discussed: stereoselective addition of one or more carbon or heteroatom groups across a C=C bond (e.g., dihydroxylation, hydroboration, hydroamination, conjugate addition), epoxidation, aziridination, and cyclopropanation.
This volume is part of a 3-volume set: Science of Synthesis Stereoselective Synthesis Workbench Edition
Further information about Stereoselective Synthesis (including sample pages and the table of contents)
"synopsis" may belong to another edition of this title.
Professor, DSM Pharmaceutical Products, Innovative Synthesis & Catalysis, Geleen, Netherlands
C=C reactions are highly attractive as they are additions, and thus by nature highly atom-economic. Specific topics discussed: stereoselective addition of one or more carbon or heteroatom groups across a C=C bond (e.g., dihydroxylation, hydroboration, hydroamination, conjugate addition), epoxidation, aziridination, and cyclopropanation.
This volume is part of a 3-volume set: Science of Synthesis Stereoselective Synthesis Workbench Edition
Further information about Stereoselective Synthesis (including sample pages and the table of contents)
"About this title" may belong to another edition of this title.
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