Pinus Jumaryatno
University of Queensland
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Pinus Jumaryatno.
Australian Journal of Chemistry | 2012
Peter L. Katavic; Pinus Jumaryatno; John N. A. Hooper; Joanne T. Blanchfield; Mary J. Garson
The isolation and structure elucidation of seven new oxygenated terpenoids and eight known terpene metabolites from marine invertebrates collected at the Inner Gneerings Reef, South East Queensland, is discussed. Investigation of the sponge Coscinoderma matthewsi yielded an epoxylactone derivative (1) of the known furanoterpene tetradehydrofurospongin-1 (2). A chemical investigation of the dissected nudibranch Chromodoris albopunctata provided the new oxygenated diterpenes 12α-acetoxyspongian-16-one (10), 20-acetoxyspongian-16-one (12), 20-oxyspongian-16-one propionate (13) and 12α,20-dioxyspongian-16- one dipropionate (14) in conjunction with three other known diterpene metabolites, while two new chromodorolides, D(17) and E(18), in addition to four known diterpenes were isolated from a Dysidea sp.
Australian Journal of Chemistry | 2013
Peter L. Katavic; Pinus Jumaryatno; John N. A. Hooper; Joanne T. Blanchfield; Mary J. Garson
The isolation and structure elucidation of seven new oxygenated terpenoids and eight known terpene metabolites from marine invertebrates collected at the Inner Gneerings Reef, South East Queensland, is discussed. Investigation of the sponge Coscinoderma matthewsi yielded an epoxylactone derivative (1) of the known furanoterpene tetradehydrofurospongin-1 (2). A chemical investigation of the dissected nudibranch Chromodoris albopunctata provided the new oxygenated diterpenes 12?-acetoxyspongian-16-one (10), 20-acetoxyspongian-16-one (12), 20-oxyspongian-16-one propionate (13) and 12?,20-dioxyspongian-16-one dipropionate (14) in conjunction with three other known diterpene metabolites, while two new chromodorolides, D (17) and E (18), in addition to four known diterpenes were isolated from a Dysidea sp.
The Open Conference Proceedings Journal | 2013
Pinus Jumaryatno; Tina S. Skinner-Adams; Katherine Thea Andrews; Rohan Andrew Davis; Joanne T. Blanchfield; Mary J. Garson
Pharmacy Department, Faculty of Mathematic and Natural Sciences, Universitas Islam Indonesia, Yogyakarta 55584, Indonesia; Eskitis Institute, Griffith University, Brisbane, QLD 4111, Australia; Queensland Institute of Medical Research, Locked Bag 2000, Herston 4029, Australia; School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD 4072, Australia; E-mail: [email protected]
Journal of Natural Products | 2007
Pinus Jumaryatno; Bronwin Stapleton; John N. A. Hooper; Douglas J. Brecknell; Joanne T. Blanchfield; Mary J. Garson
Arkivoc | 2007
Pinus Jumaryatno; K. Rands-Trevor; Joanne T. Blanchfield; Mary J. Garson
Faculty of Health | 2013
Peter L. Katavic; Pinus Jumaryatno; John N. A. Hooper; Joanne T. Blanchfield; Mary J. Garson
Faculty of Health | 2013
Peter L. Katavic; Pinus Jumaryatno; John N. A. Hooper; Joanne T. Blanchfield; Mary J. Garson
Australian Journal of Chemistry | 2013
Peter L. Katavic; Pinus Jumaryatno; John N. A. Hooper; Joanne T. Blanchfield; Mary J. Garson
Archive | 2012
Pinus Jumaryatno
Pure and Applied Chemistry | 2011
Pinus Jumaryatno; Joanne T. Blanchfield; Mary J. Garson