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Journal ArticleDOI

5-endo-Trigonal radical cyclisation—a general procedure for making five-membered rings

Derrick L. J. Clive, +1 more
- 01 Jan 1995 - 
- Iss: 3, pp 319-320
TLDR
Silicon-centred radicals, derived from alkoxy dialkyl silanes by intramolecular hydrogen transfer, undergo 5-endo-trigonal closure as mentioned in this paper.
Abstract
Silicon-centred radicals, derived from alkoxy dialkyl silanes by intramolecular hydrogen transfer, undergo 5-endo-trigonal closure.

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Journal ArticleDOI

Programmierung organischer Moleküle: Design und Management organischer Synthesen über radikalische Kaskaden

TL;DR: In this paper, a discussion of the sagenhafte Spannweite of Kaskaden unimolekularer Radikalreaktionen is presented.
Journal ArticleDOI

N-heterocyclic carbene-catalyzed hydrosilylation of styryl and propargylic alcohols with dihydrosilanes.

TL;DR: Addition of structurally diverse N-heterocyclic carbenes to silicon allows the reduction of propargylic and styryl alcohols through an organocatalyzed silylation/direct hydride transfer tandem reaction (see scheme).
References
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Journal ArticleDOI

Rules for ring closure

TL;DR: The endocyclic closure of nucleophilic centres to polarized double bonds to give five-membered rings is impeded by restrictions of geometry; these restrictions can be overcome in acid through the generation of oxonium or protonated forms.
Journal Article

Hydrogen peroxide oxidation of the silicon-carbon bond in organoalkoxysilanes

TL;DR: Scission oxydante de (diethoxy methyl octyl) silane par H 2 O 2 and conduisant a l'octanol-1 as discussed by the authors, 1
Journal ArticleDOI

Silafunctional compounds in organic synthesis. Part 20. Hydrogen peroxide oxidation of the silicon-carbon bond in organoalkoxysilanes

TL;DR: Scission oxydante de (diethoxy methyl octyl) silane par H 2 O 2 and conduisant a l'octanol-1 as mentioned in this paper, 1
Journal ArticleDOI

Oxidative cleavage of silicon-carbon bonds in organosilicon fluorides to alcohols

TL;DR: In this article, the C-Si bonds in organosilicon fluorides, K 2 (RSiF 5 ] and R n SiF 4-n, are cleaved by m-chloroperbenzoic acid (MCPBA) in DMF to give the corresponding alcohols in high yields.
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