The molybdenum-molybdenum triple bond. 15. Compounds with chains of metal atoms having M-M single and triple bonds: M2(M'(M'Me3)3)2(NMe2)4 (M.tplbond.M) where M = Mo and W and M' = Si and Sn

1984 ◽  
Vol 23 (24) ◽  
pp. 4097-4102 ◽  
Author(s):  
Malcolm H. Chisholm ◽  
Hsin Tien Chiu ◽  
Kirsten Folting ◽  
John C. Huffman
Keyword(s):  
1987 ◽  
Vol 109 (22) ◽  
pp. 6796-6816 ◽  
Author(s):  
Malcolm H. Chisholm ◽  
David L. Clark ◽  
John C. Huffman ◽  
William G. Van der Sluys ◽  
Edward M. Kober ◽  
...  

1983 ◽  
Vol 105 (9) ◽  
pp. 2606-2611 ◽  
Author(s):  
Bruce E. Bursten ◽  
F. Albert Cotton ◽  
Phillip E. Fanwick ◽  
George G. Stanley ◽  
Richard A. Walton

1983 ◽  
Vol 61 (6) ◽  
pp. 1073-1076 ◽  
Author(s):  
Suzanne R. Abrams ◽  
Donato D. Nucciarone ◽  
Warren F. Steck

The lithium and sodium salts of 1,2-diaminoethane, 1,3-diaminopropane, n-butylamine, and the lithium salt of isobutylamine were studied as potential reagents for isomerization of triple bonds in alkyn-1-ols. The sodium salts of the diamines afforded high yields of the ω-alkyn-1-ol. Somewhat surprisingly, the sodium salt of n-butylamine also effects isomerization to the terminal position. The lithium salt of 1,3-diaminopropane gave the highest conversion of 2- to 3-alkyn-1-ol. A novel, selective rearrangement of one triple bond of a diynol, a 2, ω- to 3, ω-diyn-1-ol isomerization, was incorporated into a synthesis of the insect sex pheromone 3,13-octadecadienol acetate.


2018 ◽  
Vol 54 (59) ◽  
pp. 8210-8213 ◽  
Author(s):  
Lena Winner ◽  
Alexander Hermann ◽  
Guillaume Bélanger-Chabot ◽  
Oscar F. González-Belman ◽  
J. Oscar C. Jiménez-Halla ◽  
...  
Keyword(s):  

A silylene and a 1,2-diaminoalkyne respectively cleave the strong BN triple bond in iminoboranes.


Synthesis ◽  
2021 ◽  
Author(s):  
Toshimichi Ohmura ◽  
Kaito Yagi ◽  
Takeru Torigoe ◽  
Michinori Suginome

Intramolecular addition of a C(sp3)–H bond of a dimethylamino group across a C–C triple bond in 2-alkynyl-N,N-dimethylanilines was effectively catalyzed by a new iridium complex IrCl(DTBM-SEGPHOS)(C2H4) in mesitylene at 150 °C. The intramolecular C(sp3)–H addition was followed by double bond isomerization to afford 3-substituted indoles in good to high yields.


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