TY - JOUR
T1 - A Coupling Approach for the Generation of α,α-Bis(enolate) Equivalents
T2 - Regioselective Synthesis of gem-Difunctionalized Ketones
AU - Iacono, Carmelo E.
AU - Stephens, Thomas C.
AU - Rajan, Teena S.
AU - Pattison, Graham
PY - 2018/1/30
Y1 - 2018/1/30
N2 - Regioselective α,α-difunctionalization adjacent to a ketone is a significant synthetic challenge. Here, we present a solution to this problem through the transition-metal-free coupling of esters with geminal bis(boron) compounds. This forms an α,α-bis(enolate) equivalent which can be trapped with electrophiles including alkyl halides and fluorinating agents. This presents an efficient, convergent synthetic strategy for the synthesis of unsymmetrical blocked ketones.
AB - Regioselective α,α-difunctionalization adjacent to a ketone is a significant synthetic challenge. Here, we present a solution to this problem through the transition-metal-free coupling of esters with geminal bis(boron) compounds. This forms an α,α-bis(enolate) equivalent which can be trapped with electrophiles including alkyl halides and fluorinating agents. This presents an efficient, convergent synthetic strategy for the synthesis of unsymmetrical blocked ketones.
UR - http://www.scopus.com/inward/record.url?scp=85042005955&partnerID=8YFLogxK
U2 - 10.1021/jacs.7b12941
DO - 10.1021/jacs.7b12941
M3 - Article
AN - SCOPUS:85042005955
VL - 140
SP - 2036
EP - 2040
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
SN - 1520-5126
IS - 6
ER -