Literature DB >> 17217289

Large-scale synthesis of immunoactivating natural product, pristane, by continuous microfluidic dehydration as the key step.

Katsunori Tanaka1, Shinya Motomatsu, Koichi Koyama, Shin-ichi Tanaka, Koichi Fukase.   

Abstract

An efficient protocol of dehydration was developed under microfluidic conditions. The method was applied to a multikilogram synthesis of pristane, a biologically important natural product, which is now widely used as an adjuvant for monoclonal antibody production. [reaction: see text].

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Year:  2007        PMID: 17217289     DOI: 10.1021/ol062777o

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  9 in total

Review 1.  Microfluidics for drug discovery and development: from target selection to product lifecycle management.

Authors:  Lifeng Kang; Bong Geun Chung; Robert Langer; Ali Khademhosseini
Journal:  Drug Discov Today       Date:  2007-11-26       Impact factor: 7.851

2.  Koch-Haaf reaction of adamantanols in an acid-tolerant hastelloy-made microreactor.

Authors:  Takahide Fukuyama; Yu Mukai; Ilhyong Ryu
Journal:  Beilstein J Org Chem       Date:  2011-09-15       Impact factor: 2.883

3.  Homocoupling of aryl halides in flow: Space integration of lithiation and FeCl(3) promoted homocoupling.

Authors:  Aiichiro Nagaki; Yuki Uesugi; Yutaka Tomida; Jun-Ichi Yoshida
Journal:  Beilstein J Org Chem       Date:  2011-08-02       Impact factor: 2.883

Review 4.  The synthesis of active pharmaceutical ingredients (APIs) using continuous flow chemistry.

Authors:  Marcus Baumann; Ian R Baxendale
Journal:  Beilstein J Org Chem       Date:  2015-07-17       Impact factor: 2.883

5.  Acid-mediated reactions under microfluidic conditions: a new strategy for practical synthesis of biofunctional natural products.

Authors:  Katsunori Tanaka; Koichi Fukase
Journal:  Beilstein J Org Chem       Date:  2009-08-20       Impact factor: 2.883

6.  Synthesis of unsymmetrically substituted biaryls via sequential lithiation of dibromobiaryls using integrated microflow systems.

Authors:  Aiichiro Nagaki; Naofumi Takabayashi; Yutaka Tomida; Jun-ichi Yoshida
Journal:  Beilstein J Org Chem       Date:  2009-04-29       Impact factor: 2.883

7.  Radical carbonylations using a continuous microflow system.

Authors:  Takahide Fukuyama; Md Taifur Rahman; Naoya Kamata; Ilhyong Ryu
Journal:  Beilstein J Org Chem       Date:  2009-07-13       Impact factor: 2.883

8.  Oxidative cyclization of alkenols with oxone using a miniflow reactor.

Authors:  Yoichi M A Yamada; Kaoru Torii; Yasuhiro Uozumi
Journal:  Beilstein J Org Chem       Date:  2009-04-29       Impact factor: 2.883

9.  Micro-flow synthesis and structural analysis of sterically crowded diimine ligands with five aryl rings.

Authors:  Shinichiro Fuse; Nobutake Tanabe; Akio Tannna; Yohei Konishi; Takashi Takahashi
Journal:  Beilstein J Org Chem       Date:  2013-11-01       Impact factor: 2.883

  9 in total

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