The hydroboration of most types of allylsilane is highly selective for the formation of the product having the silicon and boron in a 1,3 relationship when the hydroborating agent is 9-BBN. There is only a low degree of correlation between the difference in the chemical shifts of the trigonal carbon
โฆ LIBER โฆ
Stereochemistry in the hydroboration of allylsilanes
โ Scribed by Ian Fleming; Nicholas J Lawrence
- Book ID
- 104221249
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- French
- Weight
- 251 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
โฆ Synopsis
The hydroboration of allylsilanes is highly stereoselective in the sense (3 -t 4 and 6 + .I), especially with 9-BBN as the hydroborating reagent.
The products can be converted stereospecifically into 1,3-diol derivatives (5 and 6).
Allylsilanes usually react with electrophiles in the stereochemical sense (1). 2-4 We now report that they generally undergo hydroboration with the same stereochemistry, so that it is E+ R'sSi
๐ SIMILAR VOLUMES
Regiochemistry in the hydroboration of a
โ
Ian Fleming; Nicholas J. Lawrence
๐
Article
๐
1988
๐
Elsevier Science
๐
French
โ 272 KB
Stereochemistry of Hydroboration
โ
Hassner, Alfred; Pillar, Conrad
๐
Article
๐
1962
๐
American Chemical Society
๐
English
โ 239 KB
Stereochemistry of the hydroboration rea
โ
Kabalka, George W.; Bowman, Newell S.
๐
Article
๐
1973
๐
American Chemical Society
๐
English
โ 294 KB
The stereochemistry of the hydroboration
โ
Leslie D Field; Stephen P Gallagher
๐
Article
๐
1985
๐
Elsevier Science
๐
French
โ 201 KB
Stereochemistry of the hydroboration of
โ
Kabalka, George W.; Newton, Ray J.; Jacobus, John
๐
Article
๐
1978
๐
American Chemical Society
๐
English
โ 388 KB
Stereochemistry of hydroboration of meth
โ
Klein, Joseph.; Lichtenberg, D.
๐
Article
๐
1970
๐
American Chemical Society
๐
English
โ 438 KB