Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Michael Bodenteich"'
Autor:
Michael Bodenteich, Wendy H. Hallows, Victor E. Marquez, Barry M. Goldstein, John S. Driscoll, Joseph J. Barchi
Publikováno v:
The Journal of Organic Chemistry. 58:6009-6015
Psicoplanocin A (4a) and psico-cyclopentenylcytosine (4b) represent the first two known examples of carbocyclic ketohexose nucleosides. These two stable compound combine structural features of two known classes of natural products: neplanocin A and t
Autor:
Victor E. Marquez, Michael Bodenteich
Publikováno v:
ChemInform. 23
Protected racemic α- and β-psicofuranose were synthesized from a non-carbohydrate precursor which is available in both enantiomeric forms.
Autor:
J. J. Jun. Barchi, Michael Bodenteich, V. E. Marquez, Barry M. Goldstein, J. S. Driscoll, Wendy H. Hallows
Publikováno v:
ChemInform. 25
Publikováno v:
The Journal of Organic Chemistry. 57:2071-2076
Neplanocin F (2), a minor constituent of the family of neplanocin antibiotics, was synthesized as a racemate in 12 steps from cyclopentenone derivatives, which in turn was available from D-ribonolactone
Autor:
Victor E. Marquez, Michael Bodenteich
Publikováno v:
Tetrahedron. 48:5961-5968
Protected racemic α- and β-psicofuranose were synthesized from a non-carbohydrate precursor which is available in both enantiomeric forms.
Autor:
Victor E. Marquez, Michael Bodenteich
Publikováno v:
Nucleosides and Nucleotides. 10:311-314
Psicoplanocin A represents the first known example of a carbocyclic ketohexose nucleoside. It was synthesized in 8 steps from racemic cyclopentenone 5 which in turn is available from D-ribonolactone.
Autor:
Victor E. Marquez, Michael Bodenteich
Publikováno v:
Tetrahedron Letters. 31:5977-5980
(±)-Psicoplanocin A ( 4 ) was synthesized in 8 steps from racemic cyclopentenone 5 , which is available from D-ribonolactone.
Publikováno v:
Nucleosides, Nucleotides and Nucleic Acids. 8:855-858
Carbocyclic (+)- and (-)-(E)-5- (2-bromovinyl)-2′-deoxyuridlne have been prepared from (+)- and (-)-endo-norborn-5-en-2-y1 butyrate. In cell cultures both (+)- and (-)-C-BVDU showed activity against herpes simplex virus types 1 and 2, (+)-C-BVDU be
Publikováno v:
Journal of Medicinal Chemistry. 32:1861-1865
Both enantiomers of the carbocyclic analogues of 5-iodo-2'-deoxyuridine (14 and ent-14) and of (E)-5-(2-bromo-vinyl)-2'-deoxyuridine (16 and ent-16) were synthesized by using (+)- or (-)-endo-norborn-5-en-2-yl acetate or butyrate, respectively, as st
Publikováno v:
Monatshefte für Chemie - Chemical Monthly. 117:123-126
N-(Arylaminosulfonyl)benzamides3 were prepared by reaction of N-chlorosulfonylbenzamide or 4-chloro-N-chlorosulfonylbenzamide, resp., with isocyclic and heterocyclic amines.