Objective: To examine and evaluate improvements in cardiorespiratory fitness, psychological wellbeing, quality of life, and vocational status in postmyocardial infarction patients during and after a comprehensive 12 month exercise rehabilitation programme.
Subjects: The sample population comprised 124 patients with a clinical diagnosis of myocardial infarction (122 men and two women).
Interventions: 62 patients were randomly allocated to a regular weekly aerobic training programme, three times a week for 12 months, and compared with 62 matched controls who did not receive any formal exercise training.
J Res Natl Bur Stand A Phys Chem
January 1967
The infrared absorption spectra of two glycofuranosylacetamides and their perbenzoates, and of eleven glycopyranosylacylamides and eight esters thereof, are presented and discussed. For comparison, the spectra of thirteen 1,1-bis(acylamido)-1-deoxyalditols and eight esters thereof are also given and discussed. The useful correlations between structure and infrared absorption made by Barker and co-workers for certain carbohydrates, and by Nanasi and co-workers for some -arylglycosylamines, cannot be extended to the 1-acylamido compounds we have studied.
View Article and Find Full Text PDFJ Res Natl Bur Stand A Phys Chem
June 1961
The infrared absorption spectra of twenty pyranose acetates in the range of 5000 to 250 cm are reported. The conformation adopted by each of fourteen of the corresponding methyl glycopyranosides (or their acetates) had previously been assigned by us from a study of their infrared spectra. Analysis of the spectra revealed, for the pyranose acetates (as for the methyl glycopyranosides and their acetates), groups of absorption bands which showed a concerted shift on change of anomeric disposition.
View Article and Find Full Text PDFJ Res Natl Bur Stand A Phys Chem
February 1961
The infrared absorption spectra of five -glycopyranosylacetamides and of six acetate esters thereof are presented, together with the spectra of five related compounds, for the range of 5000 to 250 cm. Analysis of the spectra permitted assignment of characteristic group-frequencies. For comparison, the spectra of eight reducing, pyranose acetates are also given.
View Article and Find Full Text PDFJ Res Natl Bur Stand A Phys Chem
October 1960
The infrared absorption spectra of twenty-four acetylated aldopyranosides in the range of 5,000 to 250 cm are reported. The conformation adopted by each of seventeen of the corresponding glycosides had previously been assigned by us from a study of their infrared spectra. Analysis of the spectra revealed, for the acetylated glycosides (as for the parent glycosides), groups of absorption bands which showed a concerted shift on change of anomeric disposition.
View Article and Find Full Text PDFJ Res Natl Bur Stand A Phys Chem
June 1960
The conformations of twenty-four aldopyranosides have been studied by analysis of their infrared absorption spectra. The most stable conformations of twelve of the glycosides had previously been assigned by Reeves from a study of their instability factors; these conformations were assumed to apply to the crystalline state, for which the spectra had been recorded. The compounds were classified into (a) configurationally and (b) structurally related groups, and the spectra were intercompared.
View Article and Find Full Text PDFJ Res Natl Bur Stand A Phys Chem
April 1960
An improved system is presented for indicating the principal conformations of pyranoid sugars and derivatives, by attaching two symbols to the systematic name. The symbol shows the kind of pyranoid ring; for example, B = a boat, C = the chair, and S = a skew form. (The three boat and six skew rings are distinguished by subscript numerals referring to exoplanar ring-atoms.
View Article and Find Full Text PDFJ Am Pharm Assoc Am Pharm Assoc
September 1951
J Am Pharm Assoc Am Pharm Assoc
August 1951
J Am Pharm Assoc Am Pharm Assoc
February 1948