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Volumn 19, Issue 21, 1978, Pages 1847-1850

New stereospecific synthesis of cis and trans d,1-chrysanthemic esters and analogs via a common intermediate

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Indexed keywords

EID: 0002597312 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(01)94687-8 Document Type: Article

Times cited : (32)

References (14)

1
- 0002734802
- A new design for the synthesis of chrysanthemic esters and analogs And for the “pear ester” synthesis
- and references cited
- (1976) Tetrahedron Letters , pp. 3911
- Devos¹ Hevesi² Bayet³ Krief⁴

2
- 84917986155
- French Patent, A. Krief and Roussel Uclaf, Number 1770, 30/02/1976

3
- 84917986154
- French Patent, A. Krief and Roussel Uclaf, Number 1771, 30/02/1976

4
- 84917986153
- The yield given are those obtained with fumarate when DME is used as solvent. Similar yields are obtained with maleate or when THE is used in both cases

5
- 40949090658
- (1967) J. Amer. Chem. Soc. , vol.89 , pp. 3913
- Corey¹ Jautelat²

6
- 84917986152
- The construction of the carbon carbon double bond (from 6 or 11 by Wittig reaction) will not be discussed in this preliminary report because it has been already done by us and others. For the trans series see our reference 1, for the cis series see our reference 7.

7
- 0001901498
- A total stereospecific synthesis of d,1 cis and d,1 trans chrysanthemic esters
- (1976) Tetrahedron Letters , pp. 3915
- Sevrin¹ Hevesi² Krief³

10
- 49949122286
- Dipyridine-chromium(VI) oxide oxidation of alcohols in dichloromethane
- (1968) Tetrahedron Letters , pp. 3363
- Collins¹ Hess² Frank³

11
- 49549138922
- Pyridinium chlorochromate. An efficient reagent for oxidation of primary and secondary alcohols to carbonyl compounds
- (1975) Tetrahedron Letters , pp. 2647
- Corey¹ Suggs²

14
- 84917986149
- Reactions of 3-bromo or 3- iodo-pentane with triphenyl phosphine lead to mixtures of 3-pentyl triphenyl phosphonium salts and 2-pentyl triphenyl phosphonium salts. 3-pentyl triphenyi phosphonium iodide (F=190°) is prepared from 1-propyl triphenyi phosphonium iodide (nBuLi,THF) through the 1-propylidene triphenyl phosphorane which is in turn reacted with ethyl iodide (yield : 80%).

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