+++14 статей, спасибо Hands_off и marco!

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Доброго времени суток, товарищи!
Буду очень Вам благодарен за скачанные статьи:

1. Wm. A. Henderson Jr., Sheldon A. Buckler
The Nucleophilicity of Phosphines
J. Am. Chem. Soc., 1960, 82 (22), pp 5794–5800

DOI:

http://dx.doi.org/10.1021/ja01507a009

2. E. Vedejs, P. L. Fuchs
Inversion of acyclic olefins by the phosphorus betaine method. Scope and limitations
J. Am. Chem. Soc., 1973, 95 (3), pp 822–825

DOI:

http://dx.doi.org/10.1021/ja00784a032

3. Alexander J. Bridges and Gordon H. Whitham
A method for olefin inversion via phosphine oxides
J. Chem. Soc., Chem. Commun., 1974, 142 - 143,

DOI:

http://dx.doi.org/10.1039/C39740000142

4. Robert E. Ireland, Marcia I. Dawson, Steven C. Welch, Alexander. Hagenbach, Jon. Bordner, Benes. Trus
Total synthesis of terpenes, XVIII. Convergent, stereoselective total synthesis of the unsymmetrical pentacyclic triterpene alnusenone
J. Am. Chem. Soc., 1973, 95 (23), pp 7829–7841

DOI:

http://dx.doi.org/10.1021/ja00804a045

5. Irving J. Borowitz, Kenneth C. Kirby Jr., Paul E. Rusek, Edward W. R. Casper
Organophosphorus chemistry. XI. Mechanism and chirality of enol and ketophosphonium salt formation from the reactions of .alpha.-haloketones or .alpha.,.alpha.-dihaloketones with tertiary phosphines
J. Org. Chem., 1971, 36 (1), pp 88–97

DOI:

http://dx.doi.org/10.1021/jo00800a020

6. J. I. G. Cadogan and R. K. Mackie
Tervalent phosphorus compounds in organic synthesis
Chem. Soc. Rev., 1974, 3, 87 - 137,

DOI:

http://dx.doi.org/10.1039/CS9740300087

7. Larry E. Overman, Edward M. O'Connor
Nucleophilic cleavage of the sulfur-sulfur bond by phosphorus nucleophiles. IV. Kinetic study of the reduction of alkyl disulfides with triphenylphosphine and water
J. Am. Chem. Soc., 1976, 98 (3), pp 771–775

DOI:

http://dx.doi.org/10.1021/ja00419a022

8. Teruaki Mukaiyama, Rei Matsueda and Manabu Suzuki
Peptide synthesis via the oxidation-reduction condensation by the use of 2,2′-dipyridyldisulfide as an oxidant
Tetrahedron Letters, Volume 11, Issue 22, 1970, Pages 1901-1904

DOI:

http://dx.doi.org/10.1016/S0040-4039(01)98113-4

9. E. J. Corey, and Daniel J. Brunelle
New reagents for the conversion of hydroxy acids to macrolactones by the double activation method
Tetrahedron Letters, Volume 17, Issue 38, September 1976, Pages 3409-3412

DOI:

http://dx.doi.org/10.1016/S0040-4039(00)93057-0

10. Georg Wittig, Ulrich Schöllkopf
Über Triphenyl-phosphin-methylene als olefinbildende Reagenzien I
Chemische Berichte, Volume 87 Issue 9, Pages 1318 - 1330

DOI:

http://dx.doi.org/10.1002/cber.19540870919

11. Georg Wittig, Werner Haag
Über Triphenyl-phosphinmethylene als olefinbildende Reagenzien II
Chemische Berichte, Volume 88 Issue 11, Pages 1654 - 1666

DOI:

http://dx.doi.org/10.1002/cber.19550881110

12. Donald E. Bissing, A. J. Speziale
Reactions of Phosphorus Compounds. IX. The Opening of Epoxides with Tertiary Phosphines
J. Am. Chem. Soc., 1965, 87 (12), pp 2683–2690

DOI:

http://dx.doi.org/10.1021/ja01090a028

13. L. Horner, R. Luckenbach1 and W. -D. Balzer
Phosphororganische verbindungen 60 über den sterischen verlauf der quartärisierung tertiärer phosphine nach der komplexsalz-methode
Tetrahedron Letters, Volume 9, Issue 27, 1968, Pages 3157-3159

DOI:

http://dx.doi.org/10.1016/S0040-4039(00)89577-5

14. L. Cassar and M. Foa
Nickel-catalyzed synthesis of phosphonium salts
Journal of Organometallic Chemistry, Volume 74, Issue 1, 16 July 1974, Pages 75-78

DOI:

http://dx.doi.org/10.1016/S0022-328X(00)83762-6

[Hands_off]

1-7

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http://slil.ru/29240425

12

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http://slil.ru/29240446

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Hands_off, спасибо большое

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жду остальные

[macro]

8,9,13

[macro]

14

[macro]

10,11

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macro спасибо большое!