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Filters: Keyword is aldehydes  [Clear All Filters]
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A
A. K. Bhattacharya and Rana, K. C., “Amberlite-IR 120 catalyzed three-component synthesis of alpha-amino phosphonates in one-pot”, Tetrahedron Letters, vol. 49, no. 16, pp. 2598-2601, 2008.
C
V. Jha and Kumar, P., “Croncise organocatalytic route to protected (2S, 4R)-4-hydroxyornithine and(+)-pseudohygroline”, Synlett, vol. 25, no. 8, pp. 1089-1092, 2014.
A. R. Jagdale, Paraskar, A. S., and Sudalai, A., “Cu(OTf)(2) catalyzed Biginelli type condensation of aldehydes, beta-keto esters and carbamates: synthesis of 3,4-dihydro[1,3]oxazin-2-ones”, Indian Journal of Chemistry Section B-Organic Chemistry including Medicinal Chemistry, vol. 47, no. 7, pp. 1091-1095, 2008.
A. S. Paraskar and Sudalai, A., “Cu(OTf)(2) or Et3N-catalyzed three-component condensation of aldehydes, amines and cyanides: a high yielding synthesis of alpha-aminonitriles”, Tetrahedron Letters, vol. 47, no. 32, pp. 5759-5762, 2006.
E
A. K. Bhattacharya and Mujahid, M., “Efficient bakers' yeast-catalyzed multicomponent synthesis of -aminophosphonates in one pot”, Synthetic Communications, vol. 43, no. 19, pp. 2583-2589, 2013.
A. K. Bhattacharya, Mujahid, M., and Natu, A. A., “Efficient method for the synthesis of acylals from aldehydes under solvent-free conditions catalyzed by antimony trichloride”, Synthetic Communications, vol. 38, no. 1, pp. 128-134, 2008.
A. K. Bhattacharya and Kaur, T., “Efficient one-pot synthesis of alpha-amino phosphonates catalyzed by bismuth nitrate pentahydrate”, Synlett, no. 5, pp. 745-748, 2007.
U. V. Desai, Thopate, T. S., Pore, D. M., and Wadgaonkar, P. P., “Efficient, solvent-free method for the chemoselective synthesis of acylals from aldehydes and their deprotection catalyzed by silica sulfuric acid as a reusable solid acid catalyst”, Catalysis Communications, vol. 7, no. 7, pp. 508-511, 2006.
K. Venkatesan, Pujari, S. S., Lahoti, R. J., and Srinivasan, K. V., “Efficient synthesis of 1,8-dioxo-octahydro-xanthene derivatives promoted by a room temperature ionic liquid at ambient conditions under ultrasound irradiation”, Ultrasonics Sonochemistry, vol. 15, no. 4, pp. 548-553, 2008.
H
S. B. Kamble, Swami, R. K., Sakate, S. S., and Rode, C. V., “Highly efficient povidone-phosphotungstic acid catalyst for the tandem acetalization of aldehydes to bis- and tris(indolyl)methanes”, ChemPlusChem, vol. 78, no. 11, pp. 1393-1399, 2013.
R. Kumar and Chikkali, S. H., “Hydroformylation of olefins by metals other than rhodium”, Journal of Organometallic Chemistry, vol. 960, p. 122231, 2022.
I
T. Tewari, Kumar, R., and Chikkali, S. H., “Iron-catalyzed magnesium-mediated formal hydroformylation of alkynes and alkenes”, ChemCatChem, vol. 15, no. 3, 2023.
N
R. N. Reddi, Prasad, P. K., and Sudalai, A., “N-Heterocyclic carbene catalyzed oxidative coupling of alkenes/alpha-bromoacetophenones with aldehydes: a facile entry to alpha,beta-epoxy ketones”, Angewandte Chemie-International Edition, vol. 54, no. 47, pp. 14150-14153, 2015.
R. N. Reddi, Gontala, A., Prasad, P. K., and Sudalai, A., “N-heterocyclic-carbene-catalyzed regioselective oxidative ring-opening of epoxides with aromatic aldehydes: a facile entry to alpha-acyloxyketones”, Asian Journal of Organic Chemistry, vol. 5, no. 1, pp. 48-51, 2016.
O
S. P. Sawargave, Kudale, A. S., Deore, J. V., Bhosale, D. S., Divse, J. M., Chavan, S. P., and Borate, H. B., “One-step synthesis of 4-alkyl-3-aryl-2,6-dicyanoanilines and their use in the synthesis of highly functionalized 2,3,5,6,7-and 2,3,4,5,7-substituted indoles”, Tetrahedron Letters, vol. 52, no. 42, pp. 5491-5493, 2011.
V. Paul I. Raj, Suryavanshi, G., and Sudalai, A., “Organocatalytic activation of TMSCN by basic ammonium salts for efficient cyanation of aldehydes and imines”, Tetrahedron Letters, vol. 48, no. 40, pp. 7211-7214, 2007.
P
P. V. Chouthaiwale, Rawat, V., and Sudalai, A., “Pd-catalyzed selective hydrosilylation of aryl ketones and aldehydes”, Tetrahedron Letters, vol. 53, no. 2, pp. 148-150, 2012.
S
V. R. Choudhary and Dumbre, D. K., “Solvent-free selective oxidation of primary alcohols-to-aldehydes and aldehydes-to-carboxylic acids by molecular oxygen over MgO-supported nano-gold catalyst”, Catalysis Communications, vol. 13, no. 1, pp. 82-86, 2011.