Influence of reaction conditions on products of the Pictet—Spengler condensationPULKA, Karolina; MISICKA, Aleksandra.Tetrahedron (Oxford. Print). 2011, Vol 67, Num 10, issn 0040-4020, 1723, 1955-1959 [6 p.]Article

A synthesis of chiral 1,1,3-trisubstituted 1,2,3,4-tetrahydro-β-carbolines by the Pictet-Spengler reaction of tryptophan and ketones: Conversion of (1R, 3S)-diastereomers into their (1S, 3S)-counterparts by scission of the C(1)-N(2) bondHORIGUCHI, Yoshie; NAKAMURA, Masayoshi; SAITOH, Toshiaki et al.Chemical and pharmaceutical bulletin. 2003, Vol 51, Num 12, pp 1368-1373, issn 0009-2363, 6 p.Article

Synthetic Studies toward Ecteinascidin 743 (Trabectedin)IMAI, Takahiro; NAKATA, Hiyoku; YOKOSHIMA, Satoshi et al.Synthesis (Stuttgart). 2012, Num 17, pp 2743-2753, issn 0039-7881, 11 p.Article

Catalytic Pictet-Spengler reactions using Yb(OTf)₃MANABE, Kei; NOBUTOU, Daisuke; KOBAYASHI, Shu et al.Bioorganic & medicinal chemistry. 2005, Vol 13, Num 17, pp 5154-5158, issn 0968-0896, 5 p.Article

New lipophilic catechin derivatives by oxa-Pictet-Spengler reactionPOATY, Bouddah; DUMARCAY, Stéphane; PERRIN, Dominique et al.European food research & technology (Print). 2009, Vol 230, Num 1, pp 111-117, issn 1438-2377, 7 p.Article

Relative reactivities of histamine and indoleamines with acetaldehydeOHYA, Takeshi; NIITSU, Masaru.Biological & pharmaceutical bulletin. 2003, Vol 26, Num 8, pp 1215-1218, issn 0918-6158, 4 p.Article

Synthesis of a Phenanthridine Analogue of Natural Isocarbostyril AlkaloidsMARTINEZ, Andrea R; VEGA, Daniel R; AGUIRRE, José M et al.Synthesis (Stuttgart). 2012, Num 1, pp 125-129, issn 0039-7881, 5 p.Article

Efficient and suitable preparation of N-sulfonyl-1,2,3,4-tetrahydroisoquinolines and ring analogues using recyclable H₆P₂W₁₈O₆₂·24H₂O/SiO₂ catalystPASQUALE, Gustavo; RUIZ, Diego; AUTINO, Juan et al.Comptes rendus. Chimie. 2012, Vol 15, Num 9, pp 758-763, issn 1631-0748, 6 p.Article

Novel σ₁ Receptor Ligands by Oxa-Pictet-Spengler Reaction of PyrazolylethanolSCHLÄGER, Torsten; SCHEPMANN, Dirk; WÜNSCH, Bernhard et al.Synthesis (Stuttgart). 2011, Num 24, pp 3965-3974, issn 0039-7881, 10 p.Article

Synthesis of Oxacycles Employing the Oxa-Pictet―Spengler Reaction: Recent Developments and New ProspectsLARGHI, Enrique L; KAUFMAN, Teodoro S.European journal of organic chemistry (Print). 2011, Num 27, pp 5195-5231, issn 1434-193X, 37 p.Article

Enantioselective Approach to 13a-Methylphenanthroindolizidine AlkaloidsBO SU; CHUNLONG CAI; QINGMIN WANG et al.Journal of organic chemistry. 2012, Vol 77, Num 18, pp 7981-7987, issn 0022-3263, 7 p.Article

Amino acid oxidase-catalysed resolution and Pictet-Spengler reaction towards chiral and rigid unnatural amino acids : BiocatalysisBENZ, Peter; WOHLGEMUTH, Roland.Journal of chemical technology and biotechnology (1986). 2007, Vol 82, Num 12, pp 1082-1086, issn 0268-2575, 5 p.Article

Pictet-Spengler Reaction Using Ion-Exchange Resin as a Catalyst and Support for 'Catch and Release' PurificationIZUMI, Minoru; KIDO, Takeshi; MURAKAMI, Miyu et al.Bioscience, biotechnology, and biochemistry. 2011, Vol 75, Num 2, pp 391-392, issn 0916-8451, 2 p.Article

SYNTHESIS OF CORYPALLINE & ITS SPECTRAL CHARACTERISTICS.FRANSISCA MARY LJ; SUGUNA H; RAJESWARI S et al.1977; INDIAN J. CHEM., B; INDIA; DA. 1977; VOL. 15; NO 2; PP. 182-183; BIBL. 8 REF.Article

N-terminal labeling of proteins by the Pictet-Spengler reactionSASAKI, Tsubasa; KODAMA, Koichiro; SUZUKI, Hiroaki et al.Bioorganic & medicinal chemistry letters (Print). 2008, Vol 18, Num 16, pp 4550-4553, issn 0960-894X, 4 p.Article

Synthesis and biological evaluation of new tetrahydro-β-carbolines as inhibitors of the mitotic kinesin Eg5SUNDER-PLASSMANN, Nils; SARLI, Vasiliki; GARTNER, Michael et al.Bioorganic & medicinal chemistry. 2005, Vol 13, Num 22, pp 6094-6111, issn 0968-0896, 18 p.Article

Synthesis of tetrahydro-5-azaindoles and 5-azaindoles using Pictet-Spengler reaction—appreciable difference in products using different acid catalystsSHUMAILA, Abdullah M. A; PURANIK, Vedavati G; KUSURKAR, Radhika S et al.Tetrahedron (Oxford. Print). 2011, Vol 67, Num 5, issn 0040-4020, 798, 936-942 [8 p.]Article

Diastereoselective synthesis of tetrasubstituted-octahydro-3, 6-diazacarbazoles and tetrasubstituted-3,6-diazacarbazoles via double Pictet―Spengler reactionSHUMAILA, Abdullah M. A; PURANIK, Vedavati G; KUSURKAR, Radhika S et al.Tetrahedron letters. 2011, Vol 52, Num 21, issn 0040-4039, 2613, 2661-2663 [4 p.]Article

Furan Ring-Opening/Indole Ring-Closure: Pictet-Spengler-Like Reaction of 2-(o-Aminophenyl)furans with AldehydesBUTIN, Alexander V; UCHUSKIN, Maxim G; PILIPENKO, Arkady S et al.European journal of organic chemistry (Print). 2010, Num 5, pp 920-926, issn 1434-193X, 7 p.Article

α-Trifluoromethyl-β-aryl enamines in the synthesis of trifluoromethylated heterocycles by the Fischer and the Pictet-Spengler reactionsMUZALEVSKIY, Vasiliy M; NENAJDENKO, Valentine G; SHASTIN, Aleksey V et al.Tetrahedron (Oxford. Print). 2009, Vol 65, Num 36, issn 0040-4020, 7324, 7553-7561 [10 p.]Article

Design and synthesis of Pictet―Spengler condensation products that exhibit oncogenic-RAS synthetic lethality and induce non-apoptotic cell deathSKOUTA, Rachid; HAYANO, Miki; SHIMADA, Kenichi et al.Bioorganic & medicinal chemistry letters (Print). 2012, Vol 22, Num 17, pp 5707-5713, issn 0960-894X, 7 p.Article

A Pictet―Spengler Cyclisation Methodology for the Construction of Nonproteinogenic Tetrahydroisoquinoline Quaternary Amino AcidsBULMAN PAGE, Philip C; PARKES, Genna A; BUCKLEY, Benjamin R et al.Synlett (Stuttgart). 2011, Num 20, pp 3005-3007, issn 0936-5214, 3 p.Article

Concise Synthesis of (±)-Aurantioclavine through a Base-Promoted Pictet-Spengler ReactionYAMADA, Koji; NAMERIKAWA, Yuichi; HARUYAMA, Tomohiro et al.European journal of organic chemistry (Print). 2009, Num 33, pp 5752-5759, issn 1434-193X, 8 p.Article

Efficient and Diverse Synthesis of Indole DerivativesHAIXIA LIU; DÖMLING, Alexander.Journal of organic chemistry. 2009, Vol 74, Num 17, pp 6895-6898, issn 0022-3263, 4 p.Article

3D-Structure and function of strictosidine synthase : the key enzyme of monoterpenoid indole alkaloid biosynthesisSTÖCKIGT, Joachim; BARLEBEN, Leif; PANJIKAR, Santosh et al.Plant physiology and biochemistry (Paris). 2008, Vol 46, Num 3, pp 340-355, issn 0981-9428, 16 p.Article