Literature DB >> 14722968

Library generation via postcondensation modifications of isocyanide-based multicomponent reactions.

Christopher Hulme1, Hugues Bienaymé, Thomas Nixey, Balan Chenera, Wyeth Jones, Paul Tempest, Adrian L Smith.   

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Year:  2003        PMID： 14722968     DOI： 10.1016/S0076-6879(03)69024-5

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN： 0076-6879            Impact factor:   1.600


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  7 in total

Review 1.  Emerging approaches for the syntheses of bicyclic imidazo[1,2-x]-heterocycles.

Authors:  Christopher Hulme; Yeon-Sun Lee
Journal:  Mol Divers       Date:  2008-04-12       Impact factor: 2.943

2.  A novel route to synthesize libraries of quinoxalines via Petasis methodology in two synthetic operations.

Authors:  Muhammad Ayaz; Justin Dietrich; Christopher Hulme
Journal:  Tetrahedron Lett       Date:  2011-09-21       Impact factor: 2.415

Review 3.  Tetrazoles via Multicomponent Reactions.

Authors:  Constantinos G Neochoritis; Ting Zhao; Alexander Dömling
Journal:  Chem Rev       Date:  2019-02-01       Impact factor: 60.622

4.  Synthesis of Tetrazolo-Fused Benzodiazepines and Benzodiazepinones by a Two-Step Protocol Using an Ugi-Azide Reaction for Initial Diversity Generation.

Authors:  Steven Gunawan; Muhammad Ayaz; Fabio De Moliner; Brendan Frett; Christine Kaiser; Nina Patrick; Zhigang Xu; Christopher Hulme
Journal:  Tetrahedron       Date:  2012-04-26       Impact factor: 2.457

Review 5.  Emerging molecular diversity from the intra-molecular Ugi reaction: iterative efficiency in medicinal chemistry.

Authors:  Christopher Hulme; Justin Dietrich
Journal:  Mol Divers       Date:  2009-02-11       Impact factor: 3.364

6.  One-pot synthesis of tetracyclic fused imidazo[1,2-a]pyridines via a three-component reaction.

Authors:  Bo Yang; Chuanye Tao; Taofeng Shao; Jianxian Gong; Chao Che
Journal:  Beilstein J Org Chem       Date:  2016-07-18       Impact factor: 2.883

7.  Methyl isocyanide as a convertible functional group for the synthesis of spirocyclic oxindole γ-lactams via post-Ugi-4CR/transamidation/cyclization in a one-pot, three-step sequence.

Authors:  Amarendar Reddy Maddirala; Peter R Andreana
Journal:  Beilstein J Org Chem       Date:  2018-04-18       Impact factor: 2.883
  7 in total

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