Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Christopher R. A. Godfrey"'
Publikováno v:
Synlett. 2010:2721-2724
A formal synthesis of the insecticidal natural product AB3217-A involving an unusual diastereoselective benzylic oxidation is described.
Publikováno v:
Tetrahedron Letters. 39:723-726
Unsymmetrical stilbene derivatives can be prepared via intramolecular free radical ipso substitution reactions using suitably constituted vinyl sulfonate and sulfonamide tethering chains.
Publikováno v:
Tetrahedron. 51:5169-5180
Stereospecific syntheses of (2 S ,3 R ) 3-carboxyproline and (2 S ,3 R ) 3-aminoproline are reported which make use of the stereospecific alkylation of (4 S )- N -( t -butyldimethylsilyl)azetidin-2-one 4-carboxylic acid with the cyclic sulfate derive
Publikováno v:
Tetrahedron. 49:7837-7856
A stereospecific synthesis of the cyclic tetrapeptide chlamydocin via free radical homologation from a ( S )-2-amino-5-iodopentanoic acid containing cyclic tetrapeptide is described.
Autor:
Christopher R. A. Godfrey, Jack E. Baldwin, R. M. Adlington, D. W. Gollins, Christopher J. Schofield
Publikováno v:
ChemInform. 22
The first stereospecific synthesis of the naturally occuring dipeptide antibiotic, alahopcin, starting from ( L -aspartic acid is described.
Autor:
Jack E. Baldwin, J. G. Vaughan, Robert M. Adlington, D. W. Gollins, Christopher R. A. Godfrey
Publikováno v:
ChemInform. 25
Autor:
Christopher R. A. Godfrey, Marie L. Smith, Jack E. Baldwin, Andrew T. Russell, Robert M. Adlington, D. W. Gollins
Publikováno v:
ChemInform. 25
Publikováno v:
ChemInform. 24
A stereospecific synthesis of the cyclic tetrapeptide chlamydocin via free radical homologation from a ( S )-2-amino-5-iodopentanoic acid containing cyclic tetrapeptide is described.
Publikováno v:
ChemInform. 26
Publikováno v:
ChemInform. 29
Unsymmetrical stilbene derivatives can be prepared via intramolecular free radical ipso substitution reactions using suitably constituted vinyl sulfonate and sulfonamide tethering chains.