Telechelic aromatic diamines (1 1) containing an oligo-or polysiloxane chain were prepared in a 4-step synthesis. In the first step 1 -allyloxy-4-nitrobenzene (6) was synthesized and subsequently hydrosilylated with chlorodimethylsilane. In the third step the product (7) was hydrolyzed or condensed
Synthèse de polysiloxanes téléchéliques, 1. Synthèse de diols et diépoxydes
✍ Scribed by Boutevin, Bernard ;Youssef, Boulos
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1989
- Weight
- 346 KB
- Volume
- 190
- Category
- Article
- ISSN
- 0025-116X
No coin nor oath required. For personal study only.
✦ Synopsis
Telechelic poly(dimethy1siloxane)s (4, 5, 6) with acetoxy, hydroxyl or 2,3-epoxypropoxy functions as end groups were synthesized. As starting materials chloro-3-acetoxy-[or 3-(2,3epoxypropoxyl-propyldimethylsilanes (2 and 3) were prepared by hydrosilylation of the corresponding allylic derivatives with chlorodimethylsilane, and subsequently condensed with a-hydro-w-hydroxyoligo-(or poly-) dimethylsiloxanes (1 b -d) in the presence of pyridine. The hydroxyl derivatives 5 a -d were obtained by hydrolysis of the acetoxy derivatives, and the 3-(2,3-epoxypropoxy)propyl derivatives 6a, b by reaction of the diols with 1 -chloro-2,3epoxypropane.
📜 SIMILAR VOLUMES
SYNTHESE DE @TRAHYDROTHIfiNOPYRIDINES F. ELOY et A. DERYCKERE Des tetrahydrothienopyridines ont 6th obtenues par formylation reductive des thienopyridines et par reduction par le borohydrure de sodium des sels quaternaires de thienopyridinium. The reductive formylation of thienopyridines and the NaB
**Synthesis of Evernin** Two syntheses of the depside evernin **6** are described. Condensation of methyl acetoacetate and methyl crotonate followed by aromatization and reduction with __Raney__‐Ni led to methyl orsellinate **(3)**. The condensation of everninic acid **(4)**, obtained by partial me
**Synthesis of Eriodermin** The total synthesis of eriodermin (=2,7‐dichloro‐4‐formyl 3‐hydroxy‐8‐methoxy‐1,6‐dimethyl‐11__H__‐dibenzo[__b__,__e__] [1,4]dioxepin‐11‐one) is described.
## Abstract Nous recherchons systématiquement et discutons les méthodes d'obtention des esters isosélénocyaniques en vue de la préparation ultérieure de sélénosemicarbazides substituées. Les méthodes principales de préparation des esters isothiocyaniques ne sont généralement pas applicables à leur