A UNIQUE 1,4-SILYL GROUP MIGRATION FROM CARBON TO CARBON: FORMATION OF BENZYLIC SILANE IN THE REACTION OF STERICALLY HINDERED BENZYLIC TELLURIDE WITH ALKYLLITHIUM

Author(s):  
Julius Adrie Garcia ◽  
Mariko Yukimoto ◽  
Yoshiyuki Mizuhata ◽  
Norihiro Tokitoh
2018 ◽  
Vol 59 (52) ◽  
pp. 4620-4621
Author(s):  
Jozef Gonda ◽  
Miroslav Psotka ◽  
Miroslava Martinková ◽  
Simona Fazekašová ◽  
Tatiana Mitríková ◽  
...  

Synlett ◽  
1992 ◽  
Vol 1992 (02) ◽  
pp. 135-136 ◽  
Author(s):  
Michael S. Loft ◽  
David A. Widdowson ◽  
Timothy J. Mowlem

ChemInform ◽  
2010 ◽  
Vol 27 (30) ◽  
pp. no-no
Author(s):  
J. M. LASSALETTA ◽  
M. MEICHLE ◽  
S. WEILER ◽  
R. R. SCHMIDT

1996 ◽  
Vol 15 (2) ◽  
pp. 241-254 ◽  
Author(s):  
José M. Lassaletta ◽  
Michaela Meichle ◽  
Sven Weiler ◽  
Richard R. Schmidt

1982 ◽  
Vol 37 (4) ◽  
pp. 423-431 ◽  
Author(s):  
William Clegg ◽  
Uwe Klingebiel ◽  
George M. Sheldrick

KOH reacts with bis(isopropyl-trimethylsilyl)-amino-difluorosilane to give the fluoro-silanol 1. An aminofluorosiloxane 2 is obtained in the reaction of [(Me3Si)2N]2SiF2 with KOH via a 1,3-silyl-group migration. The four-membered SiOSiN ring 5 can be prepared in several steps from 1. Six-membered SiO rings 8-10 are formed in the reaction of 1,3-fluorosilanols 6 and 7 with butyllithium. Lithiated 2 reacts with PCl3 to give a four-membered P2N2 ring 11, and with 2-methyl-2-propenal to give two isomeric (2 + 4) cycloadducts 12 and 13. The silicenium ylid formed initially by thermal elimation of LiF from lithiated 2 in PE/THF cross-dimerises to give a Si2N2 ring 14. If the reaction is carried out in n-heptane, the product after recrystallisation from acetone, 16, is an isomer of 14. The crystal structures of 14 and 16 have been determined.


2013 ◽  
Vol 32 ◽  
pp. 28-31 ◽  
Author(s):  
Jens Langer ◽  
Villö K. Pálfi ◽  
Björn Schowtka ◽  
Helmar Görls ◽  
Markus Reiher

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