Remarkable ligand effect in Ni- and Pd-catalyzed bisthiolation and bisselenation of terminal alkynes:: Solving the problem of stereoselective dialkyldichalcogenide addition to the CC bond

被引:75
作者
Ananikov, Valentine P. [1 ]
Gayduk, Konstantin A. [1 ]
Beletskaya, Irina P. [2 ]
Khrustalev, Victor N. [3 ,4 ]
Antipin, Mikhail Yu. [3 ,4 ]
机构
[1] Russian Acad Sci, Zelinsky Inst Organ Chem, Moscow 119991, Russia
[2] Moscow MV Lomonosov State Univ, Dept Chem, Moscow 119899, Russia
[3] Russian Acad Sci, AN Nesmeyanov Organoelement Cpds Inst, Moscow, Russia
[4] New Mexico Highlands Univ, Dept Nat Sci, Las Vegas, NM 87701 USA
关键词
alkynes; chalcogens; heterogeneous catalysis; nickel; palladium;
D O I
10.1002/chem.200701278
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We have developed two new catalytic systems based on Ni and Pd complexes to solve the challenging problem of dialkyldichalcogenide (Alk(2)E(2); E = S, Se) addition to alkynes. A comparative study of two catalytic systems-Ni/PMe2Ph and Pd/PCy2Ph-has revealed that the Ni catalyst is superior with respect to high catalytic activity and more general scope relative to the Pd system. A novel synthetic methodology was developed for the preparation of (Z)-bis(alkylthio)alkenes and (Z)-bis(alkylseleno)alkenes from terminal alkynes with excellent stereoselectivity and high yields.
引用
收藏
页码:2420 / 2434
页数:15
相关论文
共 80 条
[11]   Mechanistic study of palladium catalyzed S-S and Se-Se bonds addition to alkynes [J].
Ananikov, VP ;
Kabeshov, MA ;
Beletskaya, IP ;
Aleksandrov, GG ;
Eremenko, IL .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 2003, 687 (02) :451-461
[12]   New approach to stereochemical structure determination of bis-selenium-subsituted alkenes [J].
Ananikov, VP ;
Beletskaya, IP .
RUSSIAN CHEMICAL BULLETIN, 2003, 52 (04) :811-816
[13]   Mechanistic investigation and new catalyst design in palladium- and platinum-catalyzed Se-Se bond addition to alkynes [J].
Ananikov, VP ;
Beletskaya, IP ;
Aleksandrov, GG ;
Eremenko, IL .
ORGANOMETALLICS, 2003, 22 (07) :1414-1421
[14]   Vinyl-vinyl coupling on late transition metals through C-C reductive elimination mechanism. A computational study [J].
Ananikov, VP ;
Musaev, DG ;
Morokuma, K .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (11) :2839-2852
[15]   Catalytic triple bond activation and vinyl-vinyl reductive coupling by Pt(IV) complexes. A density functional study [J].
Ananikov, VP ;
Musaev, DG ;
Morokuma, K .
ORGANOMETALLICS, 2001, 20 (08) :1652-1667
[16]   ENERGY-ADJUSTED ABINITIO PSEUDOPOTENTIALS FOR THE 2ND AND 3RD ROW TRANSITION-ELEMENTS [J].
ANDRAE, D ;
HAUSSERMANN, U ;
DOLG, M ;
STOLL, H ;
PREUSS, H .
THEORETICA CHIMICA ACTA, 1990, 77 (02) :123-141
[17]  
[Anonymous], 2003, SADABS V 2 03 BRUKER
[18]  
[Anonymous], 1974, ORGANIC CHEM NICKEL
[19]   Theoretical and electrochemical analysis of dissociative electron transfers proceeding through formation of loose radical anion species: Reduction of symmetrical and unsymmetrical disulfides [J].
Antonello, S ;
Benassi, R ;
Gavioli, G ;
Taddei, F ;
Maran, F .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (25) :7529-7538
[20]   Addition reaction of dialkyl disulfides to terminal alkynes catalyzed by a rhodium complex and trifluoromethanesulfonic acid [J].
Arisawa, M ;
Yamaguchi, M .
ORGANIC LETTERS, 2001, 3 (05) :763-764