An efficient and catalyst-free synthesis of trisubstituted allylic sulfones through an allylic sulfonylation reaction of Morita-Baylis-Hillman (MBH) carbonates with sodium sulfinates has been developed. Under the optimized reaction conditions, a series of trisubstituted allylic sulfones were rapidly prepared in good to excellent yields (71%–99%) with good to high selectivity (Z/E from 79:21 to >99:1). Compared with known synthetic methods, the current protocol features mild reaction temperature, high efficiency and easily available reagents
An efficient Ru-catalyzed regioselective allylic trifluoromethylthiolation reaction of allylic car...
An efficient procedure for the preparation of allylic trifluoromethanesulfones with high regiosele...
Ene-reaction of allyltrialkyltin, allylgermanes, allylsilanes and enoxysilanes with sulfur dioxide a...
An efficient and catalyst-free synthesis of trisubstituted allylic sulfones through an allylic sulfo...
A dehydrative cross-coupling of unactivated allylic alcohols with sulfinic acids was achieved under ...
Allyl carbonates undergo palladium-catalyzed decarboxylative allylation of trifluoroethyl phenyl sul...
A metal-free, open-flask protocol was developed for the preparation of allylic sulfones through dire...
A facile synthesis of trisubstituted allyl thiols and allyl thiocarbamates has been accomplished fro...
A reciprocal-activation strategy for allylic sulfination with unactivated allylic alcohols was devel...
This thesis work is dealing with the study of synthetic opportunities offered by allylsulfones and p...
An electrophilic trifluoromethylthiolation of allylic alcohols produces the corresponding allylic tr...
Allylic sulfones, owning to their widespread distributions in biologically active molecules, receive...
An efficient strategy for the preparation of allylic sulfones has been developed. In this protocol, ...
Allylsilanes underwent sila-ene reaction with sulfur dioxide in the presence of Lewis acid catalysts...
Intramolecular hydrogen bonding facilitates nucleophilic addition of sulfones to Baylis-Hillman addu...
An efficient Ru-catalyzed regioselective allylic trifluoromethylthiolation reaction of allylic car...
An efficient procedure for the preparation of allylic trifluoromethanesulfones with high regiosele...
Ene-reaction of allyltrialkyltin, allylgermanes, allylsilanes and enoxysilanes with sulfur dioxide a...
An efficient and catalyst-free synthesis of trisubstituted allylic sulfones through an allylic sulfo...
A dehydrative cross-coupling of unactivated allylic alcohols with sulfinic acids was achieved under ...
Allyl carbonates undergo palladium-catalyzed decarboxylative allylation of trifluoroethyl phenyl sul...
A metal-free, open-flask protocol was developed for the preparation of allylic sulfones through dire...
A facile synthesis of trisubstituted allyl thiols and allyl thiocarbamates has been accomplished fro...
A reciprocal-activation strategy for allylic sulfination with unactivated allylic alcohols was devel...
This thesis work is dealing with the study of synthetic opportunities offered by allylsulfones and p...
An electrophilic trifluoromethylthiolation of allylic alcohols produces the corresponding allylic tr...
Allylic sulfones, owning to their widespread distributions in biologically active molecules, receive...
An efficient strategy for the preparation of allylic sulfones has been developed. In this protocol, ...
Allylsilanes underwent sila-ene reaction with sulfur dioxide in the presence of Lewis acid catalysts...
Intramolecular hydrogen bonding facilitates nucleophilic addition of sulfones to Baylis-Hillman addu...
An efficient Ru-catalyzed regioselective allylic trifluoromethylthiolation reaction of allylic car...
An efficient procedure for the preparation of allylic trifluoromethanesulfones with high regiosele...
Ene-reaction of allyltrialkyltin, allylgermanes, allylsilanes and enoxysilanes with sulfur dioxide a...