Aldehydes undergo smooth nucleophilic addition with allyl-n-tributylstannane in the presence of sulphamic acid (5 mol%, SA) under extremely mild reaction conditions to afford the corresponding homoallylic alcohols in excellent yields with high chemoselectivity. The catalyst can be recovered by simple filtration and can be recycled in subsequent reactions. The method is simple, cost-effective and environmentally benign
Iodine efficiently catalyses the allylation of both aromatic and aliphatic aldehydes with allyltrime...
Methanol promotes the addition of allyltrimethylstannane (1a) to isobutyraldehyde (2a, 30 degrees C)...
Allylic sulfones, owning to their widespread distributions in biologically active molecules, receive...
Aldehydes undergo smooth nucleophilic addition with allyl-n-tributylstannane in the presence of sulp...
Homoallylic amines are synthesized by the three-component coupling reaction of aldehydes, anilines a...
A dehydrative cross-coupling of unactivated allylic alcohols with sulfinic acids was achieved under ...
It's easy being green! In this work, supported sulfonic acids were used as effective catalysts for d...
o-Aminoaryl ketones undergo smooth condensation with α-methylene ketones in the presence of sulfamic...
o-Aminoaryl ketones undergo smooth condensation with α-methylene ketones in the presence of sulfamic...
Aldehydes undergo smooth nucleophilic addition with allyltributylstannane in the presence of CeCl<SU...
Bulky aluminum Lewis acids such as MAD and MABR are introduced as new efficient catalysts in substoi...
A reciprocal-activation strategy for allylic sulfination with unactivated allylic alcohols was devel...
SiCl4 can be conveniently activated by catalytic amounts of dimethyl sulfoxide or other readily-avai...
This dissertation details the progress made in the catalytic, nucleophilic allylation of aldehydes, ...
Methanol promotes the addition of allyltrimethylstannane (1a) to isobutyraldehyde (2a, 30 °C) yieldi...
Iodine efficiently catalyses the allylation of both aromatic and aliphatic aldehydes with allyltrime...
Methanol promotes the addition of allyltrimethylstannane (1a) to isobutyraldehyde (2a, 30 degrees C)...
Allylic sulfones, owning to their widespread distributions in biologically active molecules, receive...
Aldehydes undergo smooth nucleophilic addition with allyl-n-tributylstannane in the presence of sulp...
Homoallylic amines are synthesized by the three-component coupling reaction of aldehydes, anilines a...
A dehydrative cross-coupling of unactivated allylic alcohols with sulfinic acids was achieved under ...
It's easy being green! In this work, supported sulfonic acids were used as effective catalysts for d...
o-Aminoaryl ketones undergo smooth condensation with α-methylene ketones in the presence of sulfamic...
o-Aminoaryl ketones undergo smooth condensation with α-methylene ketones in the presence of sulfamic...
Aldehydes undergo smooth nucleophilic addition with allyltributylstannane in the presence of CeCl<SU...
Bulky aluminum Lewis acids such as MAD and MABR are introduced as new efficient catalysts in substoi...
A reciprocal-activation strategy for allylic sulfination with unactivated allylic alcohols was devel...
SiCl4 can be conveniently activated by catalytic amounts of dimethyl sulfoxide or other readily-avai...
This dissertation details the progress made in the catalytic, nucleophilic allylation of aldehydes, ...
Methanol promotes the addition of allyltrimethylstannane (1a) to isobutyraldehyde (2a, 30 °C) yieldi...
Iodine efficiently catalyses the allylation of both aromatic and aliphatic aldehydes with allyltrime...
Methanol promotes the addition of allyltrimethylstannane (1a) to isobutyraldehyde (2a, 30 degrees C)...
Allylic sulfones, owning to their widespread distributions in biologically active molecules, receive...