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Characterization of a novel esterase isolated from intertidal flat metagenome and its tertiary alcohols synthesisOH, Ki-Hoon; NGUYEN, Giang-Son; KIM, Eun-Young et al.Journal of molecular catalysis. B, Enzymatic. 2012, Vol 80, pp 67-73, issn 1381-1177, 7 p.Article

Neutral ionic liquid [BMIm]BF4 promoted highly selective esterification of tertiary alcohols by acetic anhydrideZHIYING DUAN; YANLONG GU; YOUQUAN DENG et al.Journal of molecular catalysis. A, Chemical. 2006, Vol 246, Num 1-2, pp 70-75, issn 1381-1169, 6 p.Article

Hypervalent iodine oxidation of ethynylcarbinols: a short and efficient conversion of dihydroxy-acetonyl groups from keto groupsKITA, Y; YAKURA, T; TERASHI, H et al.Chemical and pharmaceutical bulletin. 1989, Vol 37, Num 4, pp 891-894, issn 0009-2363, 4 p.Article

Comparative analysis of tertiary alcohol esterase activity in bacterial strains isolated from enrichment cultures and from screening strain librariesHERTER, Susanne; NGUYEN, Giang-Son; THOMPSON, Mark L et al.Applied microbiology and biotechnology. 2011, Vol 90, Num 3, pp 929-939, issn 0175-7598, 11 p.Article

Synthesis of (R)-1,1,2-triphenyl-1,2-ethanediol derived phosphonatesBRODESSER, B; BRAUN, M.Phosphorus and sulfur and the related elements. 1989, Vol 44, Num 3-4, pp 217-221, issn 0308-664X, 5 p.Article

Characterization of a novel hormone-sensitive lipase family esterase from Rhizomucor miehei with tertiary alcohol hydrolysis activityYAN, Qiao-Juan; YANG, Shao-Qing; DUAN, Xiao-Jie et al.Journal of molecular catalysis. B, Enzymatic. 2014, Vol 109, pp 76-84, issn 1381-1177, 9 p.Article

The co-oxidation of conjugated enynes. A convenient synthesis of β-sulfoxy acetylenic carbinolsXIAOHENG WANG; ZHIJIE NI; XIUJING LU et al.Tetrahedron letters. 1992, Vol 33, Num 40, pp 5917-5920, issn 0040-4039Article

Synthesis and relative structure of conocephalenol, a sesquiterpene alcohol isolated from the european liverwort Conocephalum conicumTORI, M; SONO, M; NAKASHIMA, K et al.Journal of the Chemical Society. Perkin transactions. I. 1991, Num 2, pp 447-450, issn 0300-922X, 4 p.Article

Chemistry of the 1-ethylcyclopropanol cation: ring opening and ethyl lossesBOUCHOUX, G; FLAMMANG, R; MASQUETIAU, A et al.Organic mass spectrometry. 1985, Vol 20, Num 2, pp 154-155, issn 0030-493XArticle

Synthesis of cis-transoid-cis- and cis-cisoid-cis-tricyclo[6.3.0.2,6]undecan-1-olsKAKIUCHI, K; TAKEUCHI, H; TOBE, Y et al.Bulletin of the Chemical Society of Japan. 1985, Vol 58, Num 5, pp 1613-1614, issn 0009-2673Article

Variation de la vitesse de déshydratation de l'alcool t-butylique en fonction de la dose introduite de ce réactifOBRAZTSOV, P. A; VINNIK, M. I.Kinetika i kataliz. 1984, Vol 25, Num 5, pp 1135-1139, issn 0453-8811Article

Montmorillonite catalyzed dehydration of tertiary alcohols to olefinsLAKSHMI KANTAM, M; LAKSHMI SANTHI, P; FYYAZUDDIN SIDDIQUI, M et al.Tetrahedron letters. 1993, Vol 34, Num 7, pp 1185-1186, issn 0040-4039Article

Une nouvelle synthèse de peroxydes d'alkyle dissymétriques à partir d'alcools tertiaires = A new synthesis of unsymetrical dialkyl peroxides from tertiary alcoholsBOURGEOIS, M.-J; MONTAUDON, E; MAILLARD, B et al.Tetrahedron (Oxford. Print). 1993, Vol 49, Num 12, pp 2477-2484, issn 0040-4020Article

Enantiomerenreine tertiäre Alkohole durch TADDOL-vermittelte Additionen an Ketone-oder wie man ein Grignard-Reagens enantioselektiv macht = Enantiomerically pure tertiary alcohols by TADDOL-assisted additions to ketones or how to make a grignard reagent enanhoselectiveWEBER, B; SEEBACH, D.Angewandte Chemie. 1992, Vol 104, Num 1, pp 96-97, issn 0044-8249Article

Boron trifluoride etherate/halide ion, a novel reagent for the conversion of allyl, benzyl and tertiary alcohols to the halidesMANDAL, A. K; MAHAJAN, S. W.Tetrahedron letters. 1985, Vol 26, Num 32, pp 3863-3866, issn 0040-4039Article

Addition of butyl- and phenyllithium to thujonesSBARBATI NUDELMAN, N; GATTO, Z; BOHE, L et al.Journal of organic chemistry. 1984, Vol 49, Num 9, pp 1540-1544, issn 0022-3263Article

Biogenetic-type total synthesis of (±)-2-deoxystemodinoneLUPI, A; PATAMIA, M; GRGURINA, I et al.Helvetica chimica acta. 1984, Vol 67, Num 8, pp 2261-2263, issn 0018-019XArticle

IBX-mediated α-hydroxylation of α-alkynyl carbonyl systems. a convenient method for the synthesis of tertiary alcoholsKIRSCH, Stefan F.Journal of organic chemistry. 2005, Vol 70, Num 24, pp 10210-10212, issn 0022-3263, 3 p.Article

BF3.OEt2 promotes fast, mild, clean and regioselective dehydration of tertiary alcoholsPOSNER, G. H; SHULMAN-ROSKES, E. M; CHANG HO OH et al.Tetrahedron letters. 1991, Vol 32, Num 45, pp 6489-6492, issn 0040-4039Article

Synthesis of the covalent hydrate of the incorrectly assumed structure of aurintricarboxylic acid (ATA)CUSHMAN, M; KANAMATHAREDDY, S.Tetrahedron (Oxford. Print). 1990, Vol 46, Num 5, pp 1491-1498, issn 0040-4020, 8 p.Article

Deoxygenation reactions of C19-diterpenoid alkaloidsPALANIAPPAN KULANTHAIVEL; PELLETIER, S. W.Tetrahedron (Oxford. Print). 1988, Vol 44, Num 14, pp 4313-4320, issn 0040-4020Article

Decamethyl[5]pericyclyne: a novel homoconjugated cyclic polyacetyleneSCOTT, L. T; DE CICCO, G. J; HYUN, J. L et al.Journal of the American Chemical Society. 1983, Vol 105, Num 26, pp 7760-7761, issn 0002-7863Article

Steroids 35: synthesis of 16,16-dimethyl-17β-hydroxysteroidsSCHNEIDER, G; WOLFLING, J; MESKO, E et al.Steroids. 1988, Vol 51, Num 3-4, pp 317-327, issn 0039-128XArticle

C45- und C50-Carotinoide. III: Synthese von (S)-trisanhydrobacterioruberin = Caroténoïdes en C45 et C50. III: Synthèse de la (S)-trisanhydrobactériorubérine = C45- and C50-carotenoids. III: Synthesis of (S)-trisanhydrobactériorubinWOLF, J.-P; PFANDER, H.Helvetica chimica acta. 1986, Vol 69, Num 1, pp 62-68, issn 0018-019XArticle

The adamantane rearrangement of 1,2-trimethylenenorbornanes. IV: Hydride-ion abstraction in 1,2-exo-trimethylenenorbornaneKLESTER, A. M; GANTER, C.Helvetica chimica acta. 1985, Vol 68, Num 1, pp 104-109, issn 0018-019XArticle

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