References
- Eto , M. 1974 . Organophosphorus Pesticides. Organic and Biological Chemistry , Cleveland : CRC Press .
- Tramontano , A. , Ammann , A. A. and Lerner , R. A. 1988 . J. Am. Chem. Soc. , 110 : 2282 and references cited therein., For examples see
- Eckstein , F. 1983 . Angew. Chem. Int. Ed. Engl. , 22 : 423 Ann. Rev. Biochem., 54, 367 (1985).
- Bayley , H. and Staros , J. V. 1984 . Azides and Nitrenes: Reactivity and Utility , Edited by: Scriven , E. F. 433 – 490 . London : Academic Press .
- Beaucage , S. L. and Iyer , R. P. , eds. 1992 . In this reaction HN3 plays the role of tetrazole, the weak acid generally used for protonation of the diisopropylamino group Vol. 48 , 2223 Tetrahedron
- Burgers , P. M. J. and Eckstein , F. 1978 . Tetrahedron Lett. , 19 : 3835 Molecular sulphur is known to add to phosphites in the presence of a base [see for example
- Staudinger , H. and Hauser , E. 1921 . Helv. Chim. Acta , 4 : 861
- Khodak , A. A. , Gilyarov , V. A. and Kabachnik , M. I. 1974 . Zh. Obshch. Khim. , 44 : 27 Chem. Abstr., 80, 107926 1974)
- Khodak , A. A. , Gilyarov , V. A. and Kabachnik , M. I. 1974 . Zh. Obshch. Khim. , 44 : 256 Chem. Abstr., 80, 120142 (1974).
- Shioiri , T. , Ninomira , K. and Yamada , S. 1972 . J. Am. Chem. Soc. , 94 : 6203
- Teichmann , H. and Hilgetag , G. 1967 . Angew. Chem. Int. Ed. Engl. , 6 : 1013 For a treatment on the nucleophilic reactivity of the thiophosphoryl group and complexing ability of the S-atom in HSAB terms see, and references cited therein.
- Kosolapoff. , G. M. 1950 . Organophosphorus Compounds , 234 New York : (Wiley & Sons . Phosphorothionate esters are prone to undergo thiono-thiolo isomerisation in the presence of a variety of catalysts including HgCl2 but at elevated temperature
- Donner , R. , Lohs , Kh. and Holzhäuser , H. 1966 . Z. Anorg. Allg. Chem. , 347 : 156
- Kosolapoff , G. M. 1950 . Organophosphorus Compounds , 241 New York : Wiley & Sons .