TY - JOUR
T1 - Synthesis and applications of tricarbonyliron complexes of dendralenes
AU - Toombs-Ruane, Henry
AU - Osinski, Nik
AU - Fallon, Thomas
AU - Wills, Cindy
AU - Willis, Anthony C.
AU - Paddon-Row, Michael N.
AU - Sherburn, Michael S.
PY - 2011/12/2
Y1 - 2011/12/2
N2 - [3]Dendralene and [4]dendralene are converted smoothly into tricarbonyliron complexes. The structures of four complexes analyzed by DFT and single-crystal X-ray analysis show that, in contrast to free hydrocarbons, complexed dendralenes prefer a roughly in-plane conformation. The complexes are stable towards Fe(CO)3 group migration up to 150 °C. The synthetic value of Fe(CO)3 complexation in the dendralene series is demonstrated through a variety of selective synthetic manipulations (Diels-Alder reaction, dipolar cycloaddition, Simmons-Smith cyclopropanation, dihydroxylation, olefin cross metathesis) that are not achievable by direct transformation of the free hydrocarbons. Application to the synthesis of a previously unreported, highly reactive linear/cross-conjugated hydrocarbon is also described. Simplicity through complexation: Tricarbonyliron complexes of dendralenes are readily prepared and stable. They allow the formation of products that cannot be accessed directly from dendralenes, including unprecedented structures (see scheme).
AB - [3]Dendralene and [4]dendralene are converted smoothly into tricarbonyliron complexes. The structures of four complexes analyzed by DFT and single-crystal X-ray analysis show that, in contrast to free hydrocarbons, complexed dendralenes prefer a roughly in-plane conformation. The complexes are stable towards Fe(CO)3 group migration up to 150 °C. The synthetic value of Fe(CO)3 complexation in the dendralene series is demonstrated through a variety of selective synthetic manipulations (Diels-Alder reaction, dipolar cycloaddition, Simmons-Smith cyclopropanation, dihydroxylation, olefin cross metathesis) that are not achievable by direct transformation of the free hydrocarbons. Application to the synthesis of a previously unreported, highly reactive linear/cross-conjugated hydrocarbon is also described. Simplicity through complexation: Tricarbonyliron complexes of dendralenes are readily prepared and stable. They allow the formation of products that cannot be accessed directly from dendralenes, including unprecedented structures (see scheme).
KW - dendralenes
KW - density functional calculations
KW - hydrocarbons
KW - metathesis
KW - synthesis design
UR - http://www.scopus.com/inward/record.url?scp=82455210257&partnerID=8YFLogxK
U2 - 10.1002/asia.201100455
DO - 10.1002/asia.201100455
M3 - Article
SN - 1861-4728
VL - 6
SP - 3243
EP - 3250
JO - Chemistry - An Asian Journal
JF - Chemistry - An Asian Journal
IS - 12
ER -