Literature DB >> 19294720

Redox economy in organic synthesis.

Noah Z Burns1, Phil S Baran, Reinhard W Hoffmann.   

Abstract

"Economy" is referred to as the thrifty and efficient use of material resources, as the principle of "minimum effort to reach a goal." More illuminating is: "the aim to portion one's forces in order to use as little as possible of them to reach a goal." Such statements certainly apply when the goal is to synthesize a complex target molecule. Redox economy then implies the use of as few redox steps as possible in the synthetic conquest of a target compound. While any sort of economy will help to streamline the effort of total synthesis, redox economy addresses a particularly weak area in present-day total synthesis. It is not enough to point out the present deficiencies, rather the purpose of this Review is to serve as a teaching tool for all practitioners of the field by giving and illustrating guidelines to increase redox economy in multistep organic synthesis.

Year:  2009        PMID: 19294720     DOI: 10.1002/anie.200806086

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  128 in total

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Journal:  Nat Chem       Date:  2010-10       Impact factor: 24.427

5.  Design and synthesis of potential mechanism-based inhibitors of the aminotransferase BioA involved in biotin biosynthesis.

Authors:  Ce Shi; Courtney C Aldrich
Journal:  J Org Chem       Date:  2012-07-03       Impact factor: 4.354

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7.  Redox-neutral α-arylation of amines.

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Journal:  Org Lett       Date:  2013-12-13       Impact factor: 6.005

8.  Synthesis of ent-ketorfanol via a C-H alkenylation/torquoselective 6π electrocyclization cascade.

Authors:  Eric M Phillips; Tehetena Mesganaw; Ashay Patel; Simon Duttwyler; Brandon Q Mercado; Kendall N Houk; Jonathan A Ellman
Journal:  Angew Chem Int Ed Engl       Date:  2015-08-17       Impact factor: 15.336

9.  Fusarisetin A: Scalable Total Synthesis and Related Studies.

Authors:  Jing Xu; Eduardo J E Caro-Diaz; Michelle H Lacoske; Chao-I Hung; Colin Jamora; Emmanuel A Theodorakis
Journal:  Chem Sci       Date:  2012-08-23       Impact factor: 9.825

10.  Total synthesis and stereochemical assignment of (-)-ushikulide A.

Authors:  Barry M Trost; Brendan M O'Boyle; Daniel Hund
Journal:  J Am Chem Soc       Date:  2009-10-21       Impact factor: 15.419

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