Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ekaterina Y. Melikhova"'
Autor:
Ekaterina Y. Melikhova, Nolwenn Derrien, Nadia Fleary-Roberts, Siân M. Forsyth, Sofia Papadouli, Antonio M. Ruda, Vargini G. Thangavadivale, Simon N. G. Tyler, Jonathan D. Moseley
Publikováno v:
Organic Process Research & Development. 27:105-119
Autor:
Rolf Gleiter, Marina A. Taranova, Elena D. Matveeva, Nikolay S. Zefirov, Tatyana A. Podrugina, Ekaterina Y. Melikhova
Publikováno v:
Tetrahedron. 69:7395-7402
Hetaryl-substituted phosphonium–iodonium ylides with a methoxycarbonyl group as acceptor proved to be highly reactive toward various alkynes in comparison with triphenyl-substituted analogue. We were able to isolate annelated P-containing heterocyc
Publikováno v:
Angewandte Chemie (International Ed. in English)
The total synthesis of dehydromicrosclerodermin B and microsclerodermin J is described. Efficient approaches to the unusual amino acids in the target molecules were developed on the basis of a Negishi coupling (for Trp‐2‐CO2H) and Blaise reaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::734c9ba00c060e1aa81cea4fab96f54d
https://ora.ox.ac.uk/objects/uuid:8c09f6e9-5717-4943-88c4-da3470b91c5e
https://ora.ox.ac.uk/objects/uuid:8c09f6e9-5717-4943-88c4-da3470b91c5e
Autor:
Robert D. C. Pullin, Akshat H. Rathi, Ekaterina Y. Melikhova, Amber L. Thompson, Timothy J. Donohoe, Christian Winter
Publikováno v:
Organic Letters
The utility of the tethered aminohydroxylation (TA) has been demonstrated by synthesis of the complex β-amino acid residue of microsclerodermins A and B. The TA provided a regio- and stereoselective functionalization of a complex homoallylic alcohol
Autor:
Ekaterina Y. Melikhova, Megan H. Shaw, Daniel P. Kloer, William G. Whittingham, John F. Bower
Publikováno v:
ChemInform. 44
Aminocyclopropanes equipped with suitable N-directing groups undergo efficient and regioselective Rh-catalyzed carbonylative C–C bond activation. Trapping of the resultant metallacycles with tethered alkynes provides an atom-economic entry to diver
Autor:
John F. Bower, Daniel P. Kloer, Megan H. Shaw, William G. Whittingham, Ekaterina Y. Melikhova
Publikováno v:
Journal of the American Chemical Society. 135(13)
Aminocyclopropanes equipped with suitable N-directing groups undergo efficient and regioselective Rh-catalyzed carbonylative C–C bond activation. Trapping of the resultant metallacycles with tethered alkynes provides an atom-economic entry to diver