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Tetrahedron Letters

Volumn 21, Issue 9, 1980, Pages 835-838

Use of allysilanes as a new type of silylating agent for alcohols and carboxylic acids

(3) Morita, Tsuyoshi a Okamoto, Yoshiki a Sakurai, Hiroshi a

a OSAKA UNIVERSITY (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0000680954 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(00)71518-8 Document Type: Article

Times cited : (140)

References (17)

1
- 0009899160
- For recent reviews on silylation, see;
- (1970) Acc. Chem. Res. , vol.3 , pp. 299
- Klebe¹

2
- 0002264491
- (1978) Chem. Ind. , pp. 794
- Cooper¹

3
- 33845310727
- (1958) J. Org. Chem. , vol.23 , pp. 50
- Langer¹ Connell² Wender³

4
- 0005866379
- (1976) J. Am. Chem. Soc. , vol.98 , pp. 2346
- Nakamura¹ Murofushi² Shimizu³ Kuwajima⁴

5
- 0041951354
- (1978) Tetrahedron Lett. , pp. 4261
- Pinnick¹ Bal² Lajis³

6
- 0002861843
- (1974) J. Organometal. Chem. , vol.69 , pp. C15
- Calas¹ Dunogues² Dellris³ Pisciotti⁴

7
- 49549128832
- (1976) Tetrahedron Lett. , pp. 1295
- Hosomi¹ Sakurai²

8
- 0002375739
- (1978) Chem. Soc. Rev. , vol.7 , pp. 15
- Colvin¹

9
- 84918341024
- (1979) Journal of Synthetic Organic Chemistry, Japan , vol.37 , pp. 739
- Ojima¹ Fuchikami²

10
- 84918341023
- Allyltrimethylsilane is commercially available from Aldrich Chemical Company, Inc. and also is easily prepared from chlorosilane and allyl bromide in THF by the Grignard reaction.

11
- 84918341022
- The propene generated was identified as 1,2-dibromopropane by the reaction with bromine.

12
- 84918341021
- 10

13
- 37049113775
- Allyl silanes in organic synthesis: some reactions of 3-trimethylsilylcyclohex-4-ene-1,2-dicarboxylic acid and its derivatives
- (1976) Journal of the Chemical Society, Chemical Communications , pp. 679
- Carter¹ Fleming²

14
- 29644432244
- (1972) J. Am. Chem. Soc. , vol.94 , pp. 6190
- Corey¹ Venkateswarlu²

15
- 0001238865
- (1978) J. Org. Chem. , vol.43 , pp. 3649
- Barton¹ Tully²

16
- 49249153005
- 4-dimethylaminopyridine: an efficient and selective catalyst for the silylation of alcohols
- (1979) Tetrahedron Letters , pp. 99
- Chaudharg¹ Hernandez²

17
- 84918341020
- The allylsilane (a colorless liquid, bp 65 – 66 °C/47 mmHg) was prepared from the chlorosilane and allyl bromide by a similar method in the case of ref. 7.

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