2006 journal article

Modular Catalysts for Diene Cycloisomerization:  Rapid and Enantioselective Variants for Bicyclopropane Synthesis

Journal of the American Chemical Society, 128(40), 13290–13297.

By: J. Feducia*, A. Campbell*, M. Doherty* & M. Gagné*

co-author countries: United States of America 🇺🇸
MeSH headings : Alkenes / chemistry; Bridged Bicyclo Compounds / chemical synthesis; Catalysis; Cyclization; Cyclopropanes / chemical synthesis; Models, Molecular; Organoplatinum Compounds / chemistry; Phosphines / chemistry; Platinum / chemistry; Stereoisomerism
Source: Crossref
Added: February 6, 2021

Deconstructing the tridentate (triphos)Pt(II) first-generation catalysts into mixed diphosphine/monophosphine combinations (P2P) has led to new, more active catalysts for the cycloisomerization of 1,6-, and 1,7-dienes into bicyclo-[3.1.0] and -[4.1.0] products. When the diphosphine was the small bite angle dppm, reaction rates were ∼20-fold faster than with triphos, although reaction rates and diastereoselectivities were also sensitive to the monophosphine (PMe3 being optimal for rate, PPh3 being optimal for selectivity). When the diphosphine was xyl-BINAP or SEGPHOS, the catalysts were enantioselective, and enantio-ratios up to 98:2 were observed. Both sets of catalysts showed enhanced functional group tolerance in comparison to the original (triphos)Pt2+ catalyst. X-ray structures for both precatalysts are also reported.