Access the full text.
Sign up today, get DeepDyve free for 14 days.
M. Sakamoto, Fumitoshi Yagishita, Masayuki Kanehiro, Yoshio Kasashima, T. Mino, T. Fujita (2010)
Exclusive photodimerization reactions of chromone-2-carboxylic esters depending on reaction media.Organic letters, 12 20
G. Speranza, C. Morelli, A. Tubaro, G. Altinier, L. Durì, P. Manitto (2005)
Aloeresin I, an anti-inflammatory 5-methylchromone from cape aloe.Planta medica, 71 1
B. Havsteen (2002)
The biochemistry and medical significance of the flavonoids.Pharmacology & therapeutics, 96 2-3
J. Hanifin, G. Morton (1967)
NMR studies of some chromone-ketene dimethyl acetal photoadducts. Long range spin-spin coupling and conformational analysis of fused cyclobutanes.Tetrahedron Letters, 8
(2009)
Photodimerization of 3 - methoxychromone derivatives subsequently followed by Norrish type II reaction , in which the stereochemistry and the details are ambiguous
M. Mazzei, E. Sottofattori, R. Dondero, M. Ibrahim, E. Melloni, M. Michetti (1999)
N,N-dialkylaminosubstituted chromones and isoxazoles as potential anti-inflammatory agents.Farmaco, 54 7
Pranab Mandal, A. Nath, R. Venkateswaran (1996)
Facile photolytic demethoxylation of 3-methoxychromonesTetrahedron, 52
J. Hanifin, E. Cohen (1966)
Photoaddition reactions of chromomeTetrahedron Letters, 7
T. Matsui, M. Nakayama (1983)
Photochemical Synthesis of the Acetylene Adducts and Dimers of 2H- and 4H-1-BenzopyranonesBulletin of the Chemical Society of Japan, 56
S. Gupta, S. Mukerjee (1973)
Photon induced reactions - II Novel photodimer of a 3-methoy chromoneTetrahedron Letters, 14
N. Chaira, A. Ferchichi, A. Mrabet, M. Sghairoun, Ali Ahmed, Awk Ahmed, RK Robinson, SN Al-Dabeeb, S. Al-Hooti, J. Sidhu, H. Qabazard, S. Al-Maiman, D. Ahmad, W. Al-shahib, RJ Marshall, SS Al-Showiman, BN Ames, MK Shigenaga, TM Hagen, É. Bauza, C. Farra, A. Berghi, G. Oberto, D. Peyronel, N. Domloge, I. Booij, G. Piombo, J. Risterucci, M. Coupe, D. Thomas, M. Ferry, EA Elgasim, Yazeed Alyousef, AM Humeid, O. Fain, JM Fayadh, DI Freig, T. Reid, L. Loeb, RK Grizotto, RE Brunsb, JM Aguirrea, HC Menezesc, K. Guyton, T. Kensler, JS Hamada, I. Hashim, F. Sharif, Z. He, O. Ishurd, J. Kennedy, E. Kafkas, M. Koşar, N. Turemis, K. Başer, Xiaofang Luo, MJ Basile, E. Kennelly, ME Martín-Esparza, N. Martínez‐Navarrete, A. Chiralt, P. Fito, MM Ozcan, H. Hacıseferoğulları, A. Puri, R. Sahai, L. Kiran, R. Saxena, TS Tadon, KC Saxena, M. Reynes, H. Bouabidi, A. Risterucci, N. Salah, N. Miller, G. Paganga, L. Tijburg, G. Bolwell, C. Riceevans, CE Vaandercook, S. Hasegawa, V. Maier, Sabe Acker, D. Berg, Mnjl Tromp, DH Grifioen, WP Bennekom, Wjf Vijgh, A. Bast, A. Yagi, A. Kabash, N. Okamura, H. Harraguchi, SM Moustafa, TI Khalifa (2002)
Antioxidant, free radical scavenging and anti-inflammatory effects of aloesin derivatives in Aloe vera.Planta medica, 68 11
N. Okamura, N. Hine, Satomi Harada, T. Fujioka, K. Mihashi, A. Yagi (1996)
Three chromone components from Aloe vera leavesPhytochemistry, 43
K. Wakasugi, T. Misaki, K. Yamada, Y. Tanabe (2000)
Diphenylammonium triflate (DPAT): efficient catalyst for esterification of carboxylic acids and for transesterification of carboxylic esters with nearly equimolar amounts of alcoholsTetrahedron Letters, 41
A. Nath, Arun Ghosh, R. Venkateswaran (1992)
Rapid, high-yield synthesis of the marine sesquiterpenes debromoaplysin and aplysin via the acid-catalyzed rearrangement of a cyclobutachromanolJournal of Organic Chemistry, 57
J. Conrad, Bernhard Förster-Fromme, M. Constantin, V. Ondruš, S. Mika, Fadime Mert-Balci, I. Klaiber, J. Pfannstiel, W. Möller, H. Rösner, K. Förster-Fromme, U. Beifuss (2009)
Flavonoid glucuronides and a chromone from the aquatic macrophyte Stratiotes aloides.Journal of natural products, 72 5
J. Hanifin, E. Cohen (1969)
Photoaddition reactions of chromoneJournal of the American Chemical Society, 91
M. Sakamoto, Masayuki Kanehiro, T. Mino, T. Fujita (2009)
Photodimerization of chromone.Chemical communications, 17
The irradiation of methyl 2- and 3-chromonecarboxylate in the presence of various alkenes afforded cyclobutane type adducts, whose structures were established by X-ray structural analysis. Methyl 2-chromonecarboxylate showed higher photochemical reactivity than methyl 3-chromonecarboxylate, in which endo adducts were yielded as major products.
Research on Chemical Intermediates – Springer Journals
Published: Jun 20, 2012
Access the full text.
Sign up today, get DeepDyve free for 14 days.