A method for the rapid reduction of acyl chlorides to aldehydes was developed using pinacolborane(HBpin)as the reducing agent.The method exhibits excellent generality for both aromatic and aliphatic substrates,affordi...A method for the rapid reduction of acyl chlorides to aldehydes was developed using pinacolborane(HBpin)as the reducing agent.The method exhibits excellent generality for both aromatic and aliphatic substrates,affording aldehydes in isolated yields of up to 88%with broad functional group tolerance,including cyano,halogen,alkenyl,ketone,and ester groups.Moreover,the method enables gram-scale aldehyde synthesis and shows high efficiency in reducing in situ generated acyl chlorides,thereby enhancing its synthetic practicality.展开更多
Reactions of bis-scandium bridged phosphinidene complex,[LSc(μ-PAr)]_(2)(L=MeC(NDIPP)CHC(Me)(NCH_(2)CH_(2)N(^(i)Pr)_(2)),DIPP=2,6-(^(i)Pr)_(2)C_(6)H_(3);Ar=2,6-Me_(2)C_(6)H_(3))(1),with pinacolborane,catecholborane,a...Reactions of bis-scandium bridged phosphinidene complex,[LSc(μ-PAr)]_(2)(L=MeC(NDIPP)CHC(Me)(NCH_(2)CH_(2)N(^(i)Pr)_(2)),DIPP=2,6-(^(i)Pr)_(2)C_(6)H_(3);Ar=2,6-Me_(2)C_(6)H_(3))(1),with pinacolborane,catecholborane,and 9-borabicyclo[3.3.1]nonane(9-BBN)are reported.Complex 1 reacts with pinacolborane and catecholborane to give scandium pinacolate(2)and catecholate(3),showing B-O bond cleavage.These two scandium complexes contain an unusual[P(Ar)B(H)P(Ar)]^(2−)dianion,which displays aμ-η^(2):η^(2) coordination model.On the other hand,reaction of complex 1 with 9-BBN affords the B-H bond cleavage product,1,3-diphospha-2,4-diboracyclobutane(4).展开更多
文摘A method for the rapid reduction of acyl chlorides to aldehydes was developed using pinacolborane(HBpin)as the reducing agent.The method exhibits excellent generality for both aromatic and aliphatic substrates,affording aldehydes in isolated yields of up to 88%with broad functional group tolerance,including cyano,halogen,alkenyl,ketone,and ester groups.Moreover,the method enables gram-scale aldehyde synthesis and shows high efficiency in reducing in situ generated acyl chlorides,thereby enhancing its synthetic practicality.
基金the National Natural Science Foundation of China(Nos.21325210,21132002 and 21121062)the State Key Basic Research&Development Program(No.2012CB821600).
文摘Reactions of bis-scandium bridged phosphinidene complex,[LSc(μ-PAr)]_(2)(L=MeC(NDIPP)CHC(Me)(NCH_(2)CH_(2)N(^(i)Pr)_(2)),DIPP=2,6-(^(i)Pr)_(2)C_(6)H_(3);Ar=2,6-Me_(2)C_(6)H_(3))(1),with pinacolborane,catecholborane,and 9-borabicyclo[3.3.1]nonane(9-BBN)are reported.Complex 1 reacts with pinacolborane and catecholborane to give scandium pinacolate(2)and catecholate(3),showing B-O bond cleavage.These two scandium complexes contain an unusual[P(Ar)B(H)P(Ar)]^(2−)dianion,which displays aμ-η^(2):η^(2) coordination model.On the other hand,reaction of complex 1 with 9-BBN affords the B-H bond cleavage product,1,3-diphospha-2,4-diboracyclobutane(4).
