D. H. R. Barton; J. M. Beaton; L. E. Geller; M. M. Pechet. A New Photochemical Reaction1. Journal of the American Chemical Society. 1961, s. 4076–4083. DOI10.1021/ja01480a030.
The IUPAC Compendium of Chemical Terminology: The Gold Book. Příprava vydání Victor Gold. 4. vyd. Research Triangle Park, NC: International Union of Pure and Applied Chemistry (IUPAC) Dostupné online. DOI10.1351/goldbook.b00599. (anglicky) DOI: 10.1351/goldbook.
A. L. Nussbaum; E. P. Yuan; C. H. Robinson; A. Mitchell; E. P. Oliveto; J. M. Beaton; D. H. R. Barton. The Photolysis of Organic Nitrites. VII. Fragmentation of the Steroidal Side Chain. The Journal of Organic Chemistry. 1962, s. 20–23. DOI10.1021/jo01048a004.
A. Sugimoto; T. Fukuyama; Y. Sumino; M. Takagi; I. Ryu. Microflow photo-radical reaction using a compact light source: Application to the Barton reaction leading to a key intermediate for myriceric acid A. Tetrahedron. 2009, s. 1593–1598. DOI10.1016/j.tet.2008.12.063.
M. Akhtar; D. H. R. Barton; P. G. Sammes. Some Radical Exchange Reactions during Nitrite Ester Photolysis1. Journal of the American Chemical Society. 1965, s. 4601–4607. DOI10.1021/ja00948a036.
A. E. Dorigo; M. A. McCarrick; R. J. Loncharich; K. N. Houk. Transition structures for hydrogen atom transfers to oxygen. Comparisons of intermolecular and intramolecular processes, and open- and closed-shell systems. Journal of the American Chemical Society. 1990, s. 7508–7514. DOI10.1021/ja00177a009.
G. Y. Ishmuratov; R. Y. Kharisov; A. K. Shayakhmetova; L. P. Botsman; O. V. Shitikova; G. A. Tolstikov. Ozonolysis of Ricinolic Acid Derivatives and Transformations of the Ozonolysis Products under Barton Reaction Conditions. Chemistry of Natural Compounds. 2005, s. 643–649. DOI10.1007/s10600-006-0003-z.
M. Akhtar; D. H. R. Barton; P. G. Sammes. Radical Exchange during Nitrite Photolysis. Journal of the American Chemical Society. 1964, s. 3394–3395. DOI10.1021/ja01070a039.
G. Petrović; Ž. Čeković. Alkylation of remote non-activated δ-carbon atoms: Addition of δ-carbon radicals, generated by 1,5-hydrogen transfer in alkoxy radical intermediates, to activated olefins. Tetrahedron. 1999, s. 1377–1390. DOI10.1016/S0040-4020(98)01110-7.
J. Allen; R. B. Boar; J. F. McGhie; D. H. R. Barton. Nitrite photolysis in the presence of oxygen. An improved synthesis of 32-oxygenated lanostanes. Journal of the Chemical Society, Perkin Transactions 1. 1973, s. 2402. DOI10.1039/P19730002402.
D. H. R. Barton; J. M. Beaton. A Synthesis of Aldosterone Acetate. Journal of the American Chemical Society. 1960, s. 2641. DOI10.1021/ja01495a062.
E. J. Corey. Simple total synthesis of (+-)-perhydrohistrionicotoxin. Journal of the American Chemical Society. 1975, s. 430–431. DOI10.1021/ja00835a039. PMID1169269.
E. J. Corey; R. W. Hahl. Synthesis of a limonoid, azadiradione. Tetrahedron Letters. 1989, s. 3023–3026. DOI10.1016/S0040-4039(00)99392-4.
The IUPAC Compendium of Chemical Terminology: The Gold Book. Příprava vydání Victor Gold. 4. vyd. Research Triangle Park, NC: International Union of Pure and Applied Chemistry (IUPAC) Dostupné online. DOI10.1351/goldbook.b00599. (anglicky) DOI: 10.1351/goldbook.
E. J. Corey. Simple total synthesis of (+-)-perhydrohistrionicotoxin. Journal of the American Chemical Society. 1975, s. 430–431. DOI10.1021/ja00835a039. PMID1169269.