1,721,896 research outputs found
Burns, Alan James, Sumatra
No full textThis record was harvested from a previous catalogue system and will be withdrawn in 2025. Information in this record may be superseded or incomplete. Visit this record in UMA's new catalogue at: https://archives.library.unimelb.edu.au/nodes/view/374958Surname: BURNS
Given Name(s) or Initials: ALAN JAMES
Military Service Number or Last Known Location: SUMATRA
Missing, Wounded and Prisoner of War Enquiry Card Index Number: 17125186339
Item: [2016.0049.07266] "Burns, Alan James, Sumatra
Broomhall, Alan James, TX8419
No full textThis record was harvested from a previous catalogue system and will be withdrawn in 2025. Information in this record may be superseded or incomplete. Visit this record in UMA's new catalogue at: https://archives.library.unimelb.edu.au/nodes/view/373823Surname: BROOMHALL
Given Name(s) or Initials: ALAN JAMES
Military Service Number or Last Known Location: TX8419
Missing, Wounded and Prisoner of War Enquiry Card Index Number: 30347185203
Item: [2016.0049.06136] "Broomhall, Alan James, TX8419
Alan JAMES (Ed.), Quintus of Smyrna. The Trojan Epic Posthomerica.
No full textDonnet Daniel. Alan JAMES (Ed.), Quintus of Smyrna. The Trojan Epic Posthomerica. . In: L'antiquité classique, Tome 75, 2006. pp. 330-331
Hacia una necesaria reforma institucional del control de las concentraciones económica
Full text linkFil: Donaldson, Alan James. Universidad de San Andrés. Departamento de Derecho; Argentina
Synthesis of carbasugar derivatives via a "Pseudo"-C2-symmetric building block derived from arabitol
No full textDevelopment of a kinetic protection protocol for arabitol affords the "pseudo"-C2- symmetric bis-acetal 8 in good yield. Utilising a scavenging purification strategy greatly simplifies the separation of 8 from the thermodynamically more stable regioisomeric byproduct 7. The building block 8 is utilised in a series of syntheses to yield a "pseudo"-C2- symmetric and C2-symmetric 1,4-bis-epoxides in 3 and 5 steps, respectively, from 8. These bis-epoxides are then reacted with a dithiane stabilised carbanion in a Brook rearrangement mediated cyclisation to furnish carbasugar derivatives in enantiopure form. The "pseudo"-C2-symmetric bis-epoxide gives a distereomeric mixture as expected, while the CVsymmetric bis-epoxide reacts to form only one diastereomer.</p
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