[1] (a) Anaraki-Ardakani H., Nekomanesh P., Synthesis of Polyfunctionalized Pyrroles by a PPh
3-Promoted Condensation Reaction between Ammonium Acetate, Dialkyl Acetylenedicarboxylate and Arylglyoxals,
Iran. J. Chem. Chem. Eng. (IJCCE), (2017) in press.
(b) Behmadi H., Moghaddam Z. A., Poormorteza N., Beyramabadi S.A., Nezhad M.A., A four Components, One-Pot Synthesis of New Imidazole Molecular Tweezers Based on 2,4,6-Triarylpyridine as Hinge Region,
Iran. J. Chem. Chem. Eng. (IJCCE), 36(1): 11-17 (2017).;
(c) Hasaninejad A., Zare A., Zolfigol M.A., Abdeshah M., Ghaderi A., Nami-Ana F., Synthesis of Poly-Substituted Quinolines
via Friedländer Hetero-Annulation Reaction Using Silica-Supported P
2O
5 under Solvent-Free Conditions,
Iran. J. Chem. Chem. Eng. (IJCCE), 30(1): 73-81 (2011).;
(b) Guzii A.G., Makarieva T.N., Denisenko V.A., Dmitrenok P.S., Kuzmich A.S., Dyshlovoy S.A., Krasokhin V.B., Stonik V.A., Monanchocidin:
A New Apoptosis-Inducing Polycyclic Guanidine Alkaloid from the Marine Sponge
Monanchora pulchra,
Org. Lett., 12(19): 4292-4295 (2010).
(c) Tong X.G., Zhou L.L., Wang Y.H., Xia C., Wang Y., Liang M, Hou F.F., Cheng Y.X., Acortatarins A and B, Two novel Antioxidative Spiroalkaloids with a Naturally unusual Morpholine Motif from Acorus Tatarinowii,
Org. Lett., 12(8): 1844-1847 (2010).
[5] Hesketh PJ., Grunberg S.M., Gralla R.J., Warr D.G., Roila F., De Wit R., Chawla S.P., Carides A.D., Ianus J., Elmer M.E., The Oral Neurokinin-1 Antagonist Aprepitant for the Prevention of Chemotherapy-Induced Nausea and Vomiting: A Multinational, Randomized, Double-Blind, Placebo-Controlled Trial in Patients Receiving High-Dose Cisplatin—The Aprepitant Protocol 052 Study Group,
J. Clin. Oncol., 21(22): 4112-4119 (2003).
[6] Hajós M., Fleishaker J.C., Filipiak‐Reisner J.K., Brown M.T., Wong E.H., The Selective Norepinephrine Reuptake Inhibitor Antidepressant Reboxetine: Pharmacological and Clinical Profile,
CNS. Drug. Rev., 10(1): 23-44 (2004).
[8] Yao L.F., Wang Y., Huang K.W., Synthesis of Morpholine or Piperazine Derivatives Through Gold-Catalyzed Cyclization Reactions of Alkynylamines or Alkynylalcohols,
Org. Chem. Front., 2(6): 721-725 (2015).
[10] Vessally E., Hosseinian A., Edjlali L., Bekhradnia A., Esrafili M.D., New Page to Access Pyridine Derivatives: Synthesis from
N-Propargylamines,
RSC Adv., 6(75): 71662-71675 (2016).
[11] Vessally E., Hosseinian A., Edjlali L., Bekhradnia A., Esrafili M.D., New Page to Access Pyrazines and their Ring Fused Analogues: Synthesis from
N-Propargylamines,
Curr. Org. Synth., 14(4): 557-567 (2017).
[13] Vessally E., Amiri S.S., Hosseinian A., Edjlali L., New Protocols to Access Imidazoles and Their Ring Fused Analogues: Synthesis from N-Propargylamines,
RSC Adv., 7(12): 7079-7091 (2017).
[14] Vessally E., Hosseinian A., Edjlali L., Bekhradnia A., Esrafili M.D., New Route to 1,4-Oxazepane and 1,4-Diazepane Derivatives: Synthesis from
N-Propargylamines,
RSC Adv., 6(102): 99781-99793 (2016).
[15] Arshadi S., Vessally E., Edjlali L., Ghorbani-kalhor E., Hosseinzadeh-Khanmir R.,
N-propargylic β-Enaminocarbonyls: A Powerful and Versatile Building Block in Organic Synthesis.,
RSC Adv., 7(22): 13198-13211 (2017).
[16] Arshadi S., Vessally E., Edjlali L., Hosseinzadeh-Khanmir R., Ghorbani-kalhor E.,
N-Propargylamines: Versatile Building Blocks in the Construction of Thiazole Cores.,
Beilstein. J. Org. Chem. 13: 625-638 (2017).
[18] Yamamoto M., Tanaka S., Naruchi K., Yamada K., A Novel Synthesis of 2,3-Dihydro-4H-1,4-Oxazin-2-Ones and 6-mMethylene-2-Morpholinones,
Synthesis., (10): 850-852 (1982).
[20] Dai L.Z., Qi M.J., Shi Y.L., Liu X.G., Shi M., Gold(I)-Catalyzed Cascade Cyclization Reaction: Highly Regio- and Diastereoselective Intermolecular Addition of Water and Alcohols to Epoxy Alkynes,
Org. Lett., 9(16): 3191-3194 (2007).
[22] Vandavasi J.K., Hu W.P., Chen H.Y., Senadi G.C., Chen C.Y., Wang J.J., A New Approach to 1,4-Oxazines and 1,4-Oxazepines
via Base-Promoted Exo Mode Cyclization of Alkynyl Alcohols: Mechanism and DFT Studies,
Org. Lett., 14(12): 3134-3137 (2012).
[24] Chaudhuri G., Chowdhury C., Kundu, N.G., A Highly Stereoselective Synthesis of (
Z)-
N-Aryl(alkyl)-2-Arylidine-2,3-Dihydro-1,4-Benzoxazines Through Palladium Catalyzed Reactions,
Synlett., (11): 1273-1275 (1998).
[25] Kundu N.G., Chaudhuri G., Upadhyay A., Palladium-Catalyzed Heteroannulation Leading to Heterocyclic Structures with Two Heteroatoms: A Highly Regio- and Stereoselective Synthesis of (
Z)-4-Alkyl-2-Alkyl(Aryl)Idene-3,4-Dihydro-2H-1, 4-Benzoxazines and (
Z)-3-Alkyl(Aryl)Idene-4-Tosyl-3,4-Dihydro-2H-1,4-Benzoxazines,
J. Org. Chem., 66(1): 20-29 (2001).
[26] Manzo A.M., Perboni A., Broggini G., Rigamonti M., An Alternative Synthesis of 2-Alkylidene-3,4-Dihydro-2H-1,4-Benzoxazines by Intramolecular Gold-Catalyzed Hydroalkoxylation of 2-(Prop-2-yn-1-Ylamino)Phenols,
Synthesis., (1): 127-132 (2011).
[31] Barluenga J., Fernández A., Diéguez A., Rodríguez F., Fañanás F.J., Gold- or Platinum-Catalyzed Cascade Processes of Alkynol Derivatives Involving Hydroalkoxylation Reactions Followed by Prins-Type Cyclizations,
Chem. Eur. J., 15(43): 11660-11667 (2009).
[32] Alcaide B., Almendros P., Carrascosa R., Torres M.R., Gold/Acid-Cocatalyzed Regiodivergent Preparation of Bridged Ketals
via Direct Bis-Oxycyclization of Alkynic Acetonides,
Adv. Synth. Catal., 352(8): 1277-1283 (2010).