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Enantioselektive Aldol-Reaktion von tert-Butylacetat mit Hilfe von Titan-Kohlenhydrat-Komplexen = Enantioselective aldol reaction of tert-butylacetate with titanium-carbohydrate complexes aidDUTHALER, R. O; HEROLD, P; LOTTENBACH, W et al.Angewandte Chemie. 1989, Vol 101, Num 4, pp 490-491, issn 0044-8249, 2 p.Article

A reverse vinylogous aldol condensationWALBORSKY, H. M; MADHAVA REDDY, S.Journal of organic chemistry. 1988, Vol 53, Num 20, pp 4851-4852, issn 0022-3263Article

Concerning the application of the 1H NMR ABX analysis for assignment of stereochemistry to aldols deriving from aldehydes lacking β-branchesDIAS, Luiz C; AGUILAR, Andrea M; SALLES, Airton G et al.Journal of organic chemistry. 2005, Vol 70, Num 25, pp 10461-10465, issn 0022-3263, 5 p.Article

Aldehyde enolate, cross aldol reaction via tin(II) enolateKATO, J.-I; MUKAIYAMA, t.Chemistry Letters. 1983, Num 11, pp 1727-1728, issn 0366-7022Article

Stereoselective anti aldol reactions of erythrulose derivatives. Functionalized chiral d3 and d4 synthonsMURGA, Juan; RUIZ, Purificacion; FALOMIR, Eva et al.Journal of organic chemistry. 2004, Vol 69, Num 6, pp 1987-1992, issn 0022-3263, 6 p.Article

Simple and Facile L-Prolinamides Derived from Achiral Cycloalkylamines as Organocatalysts for the Highly Efficient Large-Scale Asymmetric Direct Aldol ReactionsXU, Jiang-Wei; FU, Xiang-Kai; HU, Xiao-Yan et al.Catalysis letters. 2011, Vol 141, Num 8, pp 1156-1163, issn 1011-372X, 8 p.Article

An expeditious enantioselective total synthesis of valilactoneYIKANG WU; SUN, Ya-Ping.Journal of organic chemistry. 2006, Vol 71, Num 15, pp 5748-5751, issn 0022-3263, 4 p.Article

Stereocontrolled synthesis of calyculin A : construction of the C(1)-C(14) tetraene nitrile unitBARRETT, A. G. M; EDMUNDS, J. J; HENDRIX, J. A et al.Journal of the Chemical Society. Chemical communications. 1992, Num 17, pp 1238-1240, issn 0022-4936Article

Occurrence of hydroxypropanedial in certain musts and winesGUILLOU, I; BERTRAND, A; DE REVEL, G et al.Journal of agricultural and food chemistry (Print). 1997, Vol 45, Num 9, pp 3382-3386, issn 0021-8561Article

A study on the intramolecular catalytic aldol cyclodehydration of 3,4-disubstituted 1,6-dialdehydesKURTEVA, Vanya B; AFONSO, Carlos A. M.Journal of molecular catalysis. A, Chemical. 2005, Vol 234, Num 1-2, pp 159-167, issn 1381-1169, 9 p.Article

Exploring the potential of some yeast strains in the stereoselective synthesis of aldol reaction products and its reduced 1,3-dialcohol derivativesANDREU, Cecilia; DEL OLMO, Marcelli.Journal of molecular catalysis. B, Enzymatic. 2013, Vol 92, pp 57-61, issn 1381-1177, 5 p.Article

Promiscuous protease-catalyzed aldol reactions: A facile biocatalytic protocol for carbon-carbon bond formation in aqueous mediaCHAO LI; ZHOU, Yu-Jie; NA WANG et al.Journal of biotechnology. 2010, Vol 150, Num 4, pp 539-545, issn 0168-1656, 7 p.Article

Enantiomerically enriched 1-(N,N-diisopropylcarbamoyloxy)-1,3-dimethylallyllithium : stereochemistry of the stannylation, titanation, and the homoaldol reactionZSCHAGE, O; SCHWARK, J.-R; KRÄMER, T et al.Tetrahedron (Oxford. Print). 1992, Vol 48, Num 39, pp 8377-8388, issn 0040-4020Article

Synthese d'acetoacetaldehydes mono- et di-substitues par des chaines fonctionnalisées = Synthesis of acetoacetaldehydes mono-and disulatituted by functionalized chainsCARTIER, D; LEVY, J.Tetrahedron (Oxford. Print). 1990, Vol 46, Num 15, pp 5295-5304, issn 0040-4020, 10 p.Article

Réactions secondaires de l'acétaldéhyde et des aldéhydes intermédiairesBELKIN, D. I.Žurnal prikladnoj himii. 1986, Vol 59, Num 2, pp 379-384, issn 0044-4618Article

Crystallization-Driven Asymmetric Synthesis of Pyridine-β-nitroalcohols via Discovery-Oriented Self-Resolution of a Dynamic SystemANGELIN, Marcus; VONGVILAI, Pornrapee; FISCHER, Andreas et al.European journal of organic chemistry (Print). 2010, Num 33, pp 6315-6318, issn 1434-193X, 4 p.Article

Spontaneous and diastereoselective aldol reactions of cyclic β-amino ketones in the presence of waterLAZNY, Ryszard; NODZEWSKA, Aneta; TOMCZUK, Iwona et al.Tetrahedron letters. 2011, Vol 52, Num 43, issn 0040-4039, 5543, 5680-5683 [5 p.]Article

A general way, from L-ascorbic and D-isoascorbic acids, to homochiral α-hydroxy, α,β-dihydroxy and α,β-epoxy-aldehydes, useful building blocks for the synthesis of linear oxygenated fatty acids metabolitesGRAVIER-PELLETIER, C; DUMAS, J; LE MERRER, Y et al.Journal of carbohydrate chemistry. 1992, Vol 11, Num 8, pp 969-998, issn 0732-8303Article

Synthese von D-und L-2-Amino-2-deoxyarabinose sowie von D- und L-1,4-Didesoxy-1,4-iminolyxit durch (C2 + C3)-Nitroaldol-Addition mit 2-0-BenzylglycerinaldehydVON WEHNER, V; JÄGER, V.Angewandte Chemie. 1990, Vol 102, Num 10, pp 1180-1182, issn 0044-8249Article

A very short, highly efficient synthesis of natural (-)-warburganalNAKANO, T; MARTIN, A.Journal of chemical research. Synopses (Print). 1989, Num 2, pp 52-53, issn 0308-2342Article

Autocatalysis and apparent bistability in the formose reactionHUSKEY, W. P; EPSTEIN, I. R.Journal of the American Chemical Society. 1989, Vol 111, Num 9, pp 3157-3163, issn 0002-7863Article

Acid-catalyzed enolization and aldol condensation of acetaldehydeBAIGRIE, L. M; COX, R. A; SLEBOCKA-TILK, H et al.Journal of the American Chemical Society. 1985, Vol 107, Num 12, pp 3640-3645, issn 0002-7863Article

Preparation and application of 2-(arylmethoxy)isopinocampheols for the asymmetric aldol reaction of 3,3,3-trifluoropropionatesVEERARAGHAVAN RAMACHANDRAN, P; PARTHASARATHY, Gowrisankar; GAGARE, Pravin D et al.Tetrahedron letters. 2011, Vol 52, Num 41, issn 0040-4039, 5206, 5359-5362 [5 p.]Article

Discovery of a novel class of aldol-derived 1,2,3-triazoles: Potent and selective inhibitors of human cytochrome P450 19A1 (aromatase)MCNULTY, James; NAIR, Jerald J; VURGUN, Nesrin et al.Bioorganic & medicinal chemistry letters (Print). 2012, Vol 22, Num 1, pp 718-722, issn 0960-894X, 5 p.Article

L-Valine Dipeptide Organocatalysts with Two Amide Units for the Direct Asymmetric Aldol Reaction in BrineWENBO HUANG; HUA TIAN; HAO XU et al.Catalysis letters. 2011, Vol 141, Num 6, pp 872-876, issn 1011-372X, 5 p.Article

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