Literature DB >> 15624974

Skeletal diversity via a folding pathway: synthesis of indole alkaloid-like skeletons.

Hiroki Oguri1, Stuart L Schreiber.   

Abstract

Inspired by the skeletal diversity of naturally occurring indole alkaloids and the rich potential of chemistry developed by Padwa and co-workers, we conceived a pathway entailing six modes of intramolecular reactions leading to indole alkaloid-like skeletons. In this context, an efficient folding pathway via a rhodium-catalyzed tandem cyclization-cycloaddition involving three of the modes has been developed (two of which are shown above) that affords densely functionalized compounds with three distinct skeletons in a stereocontrolled manner.

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Year:  2005        PMID: 15624974     DOI: 10.1021/ol047945w

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


  16 in total

1.  Diversity-oriented synthesis as a tool for the discovery of novel biologically active small molecules.

Authors:  Warren R J D Galloway; Albert Isidro-Llobet; David R Spring
Journal:  Nat Commun       Date:  2010-09-21       Impact factor: 14.919

Review 2.  Chemical probes and drug leads from advances in synthetic planning and methodology.

Authors:  Christopher J Gerry; Stuart L Schreiber
Journal:  Nat Rev Drug Discov       Date:  2018-04-13       Impact factor: 84.694

3.  Solid-phase synthesis and chemical space analysis of a 190-membered alkaloid/terpenoid-like library.

Authors:  Gustavo Moura-Letts; Christine M Diblasi; Renato A Bauer; Derek S Tan
Journal:  Proc Natl Acad Sci U S A       Date:  2011-03-30       Impact factor: 11.205

4.  Modification of small molecules by using cytochrome P450 expressed in Escherichia coli.

Authors:  Tomohide Uno; Atsushi Nakao; Satoko Masuda; Yuuki Taniguchi; Kengo Kanamaru; Hiroshi Yamagata; Masahiko Nakamura; Hiromasa Imaishi; Kiyoharu Oono
Journal:  J Ind Microbiol Biotechnol       Date:  2006-08-05       Impact factor: 3.346

5.  Bio-inspired synthesis yields a tricyclic indoline that selectively resensitizes methicillin-resistant Staphylococcus aureus (MRSA) to β-lactam antibiotics.

Authors:  Jessica D Podoll; Yongxiang Liu; Le Chang; Shane Walls; Wei Wang; Xiang Wang
Journal:  Proc Natl Acad Sci U S A       Date:  2013-09-09       Impact factor: 11.205

6.  The tert-butylsulfinamide lynchpin in transition-metal-mediated multiscaffold library synthesis.

Authors:  Renato A Bauer; Christine M DiBlasi; Derek S Tan
Journal:  Org Lett       Date:  2010-05-07       Impact factor: 6.005

7.  A unified synthetic approach to polyketides having both skeletal and stereochemical diversity.

Authors:  Shiying Shang; Hayato Iwadare; Daniel E Macks; Lisa M Ambrosini; Derek S Tan
Journal:  Org Lett       Date:  2007-04-17       Impact factor: 6.005

8.  Explorations of stemona alkaloid-inspired analogues: skeletal modification and functional group diversification.

Authors:  Kevin J Frankowski; Benjamin Neuenswander; Jeffrey Aubé
Journal:  J Comb Chem       Date:  2008-08-13

9.  Emulating the logic of monoterpenoid alkaloid biogenesis to access a skeletally diverse chemical library.

Authors:  Song Liu; John S Scotti; Sergey A Kozmin
Journal:  J Org Chem       Date:  2013-08-27       Impact factor: 4.354

10.  Synthesis and profiling of a diverse collection of azetidine-based scaffolds for the development of CNS-focused lead-like libraries.

Authors:  Jason T Lowe; Maurice D Lee; Lakshmi B Akella; Emeline Davoine; Etienne J Donckele; Landon Durak; Jeremy R Duvall; Baudouin Gerard; Edward B Holson; Adrien Joliton; Sarathy Kesavan; Berenice C Lemercier; Haibo Liu; Jean-Charles Marié; Carol A Mulrooney; Giovanni Muncipinto; Morgan Welzel-O'Shea; Laura M Panko; Ann Rowley; Byung-Chul Suh; Meryl Thomas; Florence F Wagner; Jingqiang Wei; Michael A Foley; Lisa A Marcaurelle
Journal:  J Org Chem       Date:  2012-08-10       Impact factor: 4.354

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