TY - CHAP
T1 - Electrophilic Cyclization
AU - Jiang, X.
AU - Liu, H.
PY - 2014/2
Y1 - 2014/2
N2 - Electrophilic cyclization reaction has been demonstrated as an efficient tool in the synthesis of a great variety of heterocyclic compounds in many different ring sizes. The rings can be constructed through endo or exo cyclization modes, depending on the different substrates and electrophiles employed. Numerous electrophiles, such as halonium ions (I+, Br+, Cl+, F+), Se, S, Hg, Au, Ag, and Pt could successfully promote the electrophilic cyclizations. These electrophilic cyclization reactions could proceed under relatively mild conditions and tolerate all kinds of functional groups. Most of these methodologies proceed stereo- and regioselectively in excellent yields. In recent years, electrophilic cyclizations have been widely used in the synthesis of pharmaceuticals and natural products. A large number of publications in this field are present. Focusing on the applications of electrophilic cyclization in organic synthesis, the literatures after 1991 are summarized in this chapter, and they are sorted by different electrophiles.
AB - Electrophilic cyclization reaction has been demonstrated as an efficient tool in the synthesis of a great variety of heterocyclic compounds in many different ring sizes. The rings can be constructed through endo or exo cyclization modes, depending on the different substrates and electrophiles employed. Numerous electrophiles, such as halonium ions (I+, Br+, Cl+, F+), Se, S, Hg, Au, Ag, and Pt could successfully promote the electrophilic cyclizations. These electrophilic cyclization reactions could proceed under relatively mild conditions and tolerate all kinds of functional groups. Most of these methodologies proceed stereo- and regioselectively in excellent yields. In recent years, electrophilic cyclizations have been widely used in the synthesis of pharmaceuticals and natural products. A large number of publications in this field are present. Focusing on the applications of electrophilic cyclization in organic synthesis, the literatures after 1991 are summarized in this chapter, and they are sorted by different electrophiles.
KW - Ag-catalyzed cyclization
KW - Au-catalyzed cyclization
KW - Baldwin's rules
KW - Electrophile
KW - Electrophilic cyclization
KW - Halocyclization
KW - Hg-catalyzed cyclization
KW - Nucleophile
KW - Pt-catalyzed cyclization
KW - Selenocyclization
KW - Sulfenylcyclization
KW - Tellurolactonization
UR - https://www.scopus.com/pages/publications/84903506590
U2 - 10.1016/B978-0-08-097742-3.00409-2
DO - 10.1016/B978-0-08-097742-3.00409-2
M3 - 章节
AN - SCOPUS:84903506590
SN - 9780080977430
VL - 4
SP - 412
EP - 494
BT - Additions to and Substitutions at C-C π-Bonds
PB - Elsevier Ltd
ER -