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Rebecca J M Goss

Showing results (1-10 of 63) with videos related to

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Chemical Communications (Cambridge, England)|August 3, 2005
A novel fluorinated erythromycin antibioticRebecca J M Goss, Hui Hong
Nature Chemical Biology|September 15, 2014
Enzymology: A radical findingRebecca J M Goss, Sabine Grüschow
ACS Catalysis|May 14, 2023
Fully Aqueous and Air-Compatible Cross-Coupling of Primary Alkyl Halides with Aryl Boronic Species: A Possible and Facile MethodSamuel Molyneux, Rebecca J M Goss
Chemical Communications (Cambridge, England)|August 30, 2011
Highlights from the 46th EUCHEM Conference on stereochemistry, Bürgenstock, Switzerland, May 2011Edward W Tate, Rebecca J M Goss
Chemical Communications (Cambridge, England)|December 1, 2006
A convenient enzymatic synthesis of L-halotryptophansRebecca J M Goss, Philip L A Newill
Natural Product Reports|June 30, 2012
The generation of "unnatural" products: synthetic biology meets synthetic chemistryRebecca J M Goss, Sreejith Shankar, Antoine Abou Fayad
Natural Product Reports|May 18, 2011
The saponins: polar isoprenoids with important and diverse biological activitiesAnne Osbourn, Rebecca J M Goss, Robert A Field
Bioengineered Bugs|August 11, 2011
Revealing the first uridyl peptide antibiotic biosynthetic gene cluster and probing pacidamycin biosynthesisEmma J Rackham, Sabine Grüschow, Rebecca J M Goss
Current Opinion in Chemical Biology|February 26, 2013
Scope and potential of halogenases in biosynthetic applicationsDuncan R M Smith, Sabine Grüschow, Rebecca J M Goss
Journal of the American Chemical Society|January 9, 2003
Assay for the enantiomeric analysis of [2H1]-fluoroacetic acid: insight into the stereochemical course of fluorination during fluorometabolite biosynthesis in streptomyces cattleyaDavid O'Hagan, Rebecca J M Goss, Abdelkrim Meddour, et al.
Pageof 7

Showing results (1-10 of 63) with videos related to

Sort By:
Pageof 7
Chemical Communications (Cambridge, England)|August 3, 2005
A novel fluorinated erythromycin antibioticRebecca J M Goss, Hui Hong
Nature Chemical Biology|September 15, 2014
Enzymology: A radical findingRebecca J M Goss, Sabine Grüschow
ACS Catalysis|May 14, 2023
Fully Aqueous and Air-Compatible Cross-Coupling of Primary Alkyl Halides with Aryl Boronic Species: A Possible and Facile MethodSamuel Molyneux, Rebecca J M Goss
Chemical Communications (Cambridge, England)|August 30, 2011
Highlights from the 46th EUCHEM Conference on stereochemistry, Bürgenstock, Switzerland, May 2011Edward W Tate, Rebecca J M Goss
Chemical Communications (Cambridge, England)|December 1, 2006
A convenient enzymatic synthesis of L-halotryptophansRebecca J M Goss, Philip L A Newill
Natural Product Reports|June 30, 2012
The generation of "unnatural" products: synthetic biology meets synthetic chemistryRebecca J M Goss, Sreejith Shankar, Antoine Abou Fayad
Natural Product Reports|May 18, 2011
The saponins: polar isoprenoids with important and diverse biological activitiesAnne Osbourn, Rebecca J M Goss, Robert A Field
Bioengineered Bugs|August 11, 2011
Revealing the first uridyl peptide antibiotic biosynthetic gene cluster and probing pacidamycin biosynthesisEmma J Rackham, Sabine Grüschow, Rebecca J M Goss
Current Opinion in Chemical Biology|February 26, 2013
Scope and potential of halogenases in biosynthetic applicationsDuncan R M Smith, Sabine Grüschow, Rebecca J M Goss
Journal of the American Chemical Society|January 9, 2003
Assay for the enantiomeric analysis of [2H1]-fluoroacetic acid: insight into the stereochemical course of fluorination during fluorometabolite biosynthesis in streptomyces cattleyaDavid O'Hagan, Rebecca J M Goss, Abdelkrim Meddour, et al.
Pageof 7