TY - JOUR
T1 - Transient directing groups for the most straightforward arylation of C(sp 3 )-H bonds
AU - Kumada, Kanako
PY - 2019/1/1
Y1 - 2019/1/1
N2 - Transition-metal catalyzed C(sp 3 )-H functionalization is one of the most attractive reaction because it enables straightforward and economical syntheses of organic compounds. In the past decades, C(sp 3 )-H functionalization approaches using directing groups have been developed, however, their stoichiometric installation and removal of directing groups limit efficiency. Recently, a "transient directing group" strategy has been emerged as the solution of this program. This review highlights recent advances in C(sp 3 -H arylation using a "transient directing group".
AB - Transition-metal catalyzed C(sp 3 )-H functionalization is one of the most attractive reaction because it enables straightforward and economical syntheses of organic compounds. In the past decades, C(sp 3 )-H functionalization approaches using directing groups have been developed, however, their stoichiometric installation and removal of directing groups limit efficiency. Recently, a "transient directing group" strategy has been emerged as the solution of this program. This review highlights recent advances in C(sp 3 -H arylation using a "transient directing group".
UR - http://www.scopus.com/inward/record.url?scp=85060897661&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85060897661&partnerID=8YFLogxK
U2 - 10.5059/yukigoseikyokaishi.77.69
DO - 10.5059/yukigoseikyokaishi.77.69
M3 - Article
AN - SCOPUS:85060897661
SP - 69
EP - 70
JO - Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
JF - Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
SN - 0037-9980
ER -