3a-BF4 To a wlution of I-BF, (0.46g. 1 mmol) in dichloromethane (5 mL) at ~ 50 c' wiis added palladium tetrakis(tripheny1phosphane) (0.86 g. 0 75 mmolj. After \tirriiig for 1X h a t 40 C. the solvent was removed in vacuo. and the reziduc w a \ washed several times with toluene andether to give 3a-BF
Synthesis and Molecular Structure of the Solvent-Free [LiN(SiMe3)(2,6iPr2C6H3)]2 Dimer
β Scribed by Kennepohl, Dietmar K. ;Brooker, Sally ;Sheldrick, George M. ;Roesky, Herbert W.
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1991
- Tongue
- English
- Weight
- 306 KB
- Volume
- 124
- Category
- Article
- ISSN
- 0009-2940
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β¦ Synopsis
Abstract
[LiN(SiMe~3~)Ar]~2~ (1, Ar = 2,6β__i__Pr~2~C~6~H~3~) is prepared by the reaction of HN(SiMe~3~)Ar with __n__BuLi in nβhexane. This compound with an unusual structure contains a fourβmembered [LiN]~2~ heterocycle with two solventβfree twoβcoordinate Li centers. Its molecular structure represents the first solidβstate Xβray analysis of an uncomplexed [LiN]~2~ dimer.
π SIMILAR VOLUMES
portance for developing and carrying out syntheses of such complex, sensitive glycopeptides, since it defines the conditions under which the efficient tert-butyl protecting groups can be employed in the synthesis of polyfunctional glycoconjugates. It also explains the observed stability of serine an
The silanediols RN(SiMe3)Si(OSiMe3)(0H)2 (R = 2,4,6-were characterized by means of mass, IR and NMR (lH and Me3C6H2 4, 2,6-Me2C6H3 5 , and 2,6-iPr2C6H3 6) were prepa-2gSi) spectroscopy. Additionally, the molecular structures of red by the reactions of the respective silanetriols RN(SiMe3)-4 and 7 we