About: Pictet-Spengler reactions for the synthesis of pharmaceutically relevant heterocycles.

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About: Pictet-Spengler reactions for the synthesis of pharmaceutically relevant heterocycles. Goto Sponge NotDistinct Permalink

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scientific article published on January 2010

Attributes	Values
rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) artículu científicu espublizáu en 2010 (ast) наукова стаття, опублікована в січні 2010 (uk) scientific article published on January 2010 (en) مقالة علمية نشرت في يناير 2010 (ar)
publication date	wds:Q37808151-D387CAB7-B375-45D3-AA6C-61F534DFB0F5
publication date	2010-01-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q37808151-0B79E72D-A7B7-4674-9074-89D43AC9D113
author name string	Karolina Pulka
rdfs:label	Pictet-Spengler reactions for the synthesis of pharmaceutically relevant heterocycles. (en) Pictet-Spengler reactions for the synthesis of pharmaceutically relevant heterocycles. (nl) Pictet-Spengler reactions for the synthesis of pharmaceutically relevant heterocycles. (ast)
skos:prefLabel	Pictet-Spengler reactions for the synthesis of pharmaceutically relevant heterocycles. (en) Pictet-Spengler reactions for the synthesis of pharmaceutically relevant heterocycles. (nl) Pictet-Spengler reactions for the synthesis of pharmaceutically relevant heterocycles. (ast)
name	Pictet-Spengler reactions for the synthesis of pharmaceutically relevant heterocycles. (en) Pictet-Spengler reactions for the synthesis of pharmaceutically relevant heterocycles. (nl) Pictet-Spengler reactions for the synthesis of pharmaceutically relevant heterocycles. (ast)
title	wds:Q37808151-61857515-356F-44CD-B237-2255884FA930
title	Pictet-Spengler reactions for the synthesis of pharmaceutically relevant heterocycles (en)
page(s)	wds:Q37808151-AA32B9BA-522F-42A2-A9D6-4F7EC3B20127
page(s)	669-684
instance of	wds:Q37808151-2E9CB324-44D2-4765-856F-5865FB2E09D6
instance of	scholarly article
PubMed ID	wds:Q37808151-A42BE0BB-F5BF-4DC1-A84A-405F04F566AA
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/21061230
PubMed ID	21061230
published in	wds:Q37808151-845F311B-A4CB-4A90-8E9B-E66332FFEDF6
published in	Current Opinion in Drug Discovery and Development
issue	wds:Q37808151-6578F91C-6D4D-4AB3-86E7-248D39E62B56
volume	wds:Q37808151-4E2E2B29-65D8-48C2-A9C8-24D94D69376C
issue	6
volume	13
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q37808151
is cites work of	Thiourea-catalyzed enantioselective iso-Pictet-Spengler reactions Enantioselective Pictet-Spengler Reactions of Isatins for the Synthesis of Spiroindolones Chiral Thioureas Promote Enantioselective Pictet-Spengler Cyclization by Stabilizing Every Intermediate and Transition State in the Carboxylic Acid-Catalyzed Reaction. Phosphine-Catalyzed [3+2] and [4+3]Annulation Reactions of C,N-Cyclic Azomethine Imines with Allenoates The Pictet-Spengler Reaction Updates Its Habits Development of the Vinylogous Pictet-Spengler Cyclization and Total Synthesis of (±)-Lundurine A. Chiral Brønsted Acid-Catalyzed Enantioselective α-Amidoalkylation Reactions: A Joint Experimental and Predictive Study Phenolic Activation in Chiral Brønsted Acid-Catalyzed Intramolecular α-Amidoalkylation Reactions for the Synthesis of Fused Isoquinolines Green Routes for the Production of Enantiopure Benzylisoquinoline Alkaloids.
is cites work of	wds:Q92815392-E04EA010-1067-4B5C-8974-EB2749034C2D wds:Q48056382-E1989C2A-58D8-4BF2-9CCA-7693E7771CBB wds:Q38908265-DBC18F6D-9D81-4F20-B8BA-78661D296DF4 wds:Q39339733-88BDB423-FEF3-4E4A-8FDB-C740C54946BE wds:Q35840070-9FF3B59C-2F0B-4A09-BE19-48A36512F6CC wds:Q52583764-84E181AA-F81B-442F-87E4-C5705DAAFABC wds:Q92928566-C0DC5DBF-027C-49E6-BDE1-D3FD5E1E11FC wds:Q34706915-1B1E67D1-D917-43AC-8F22-1474B6A01011 wds:Q47151515-35E410EE-98DD-4233-A08B-BF60314C445C

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