Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Kasey Wood"'
Autor:
Kasey Wood, BS, Marina Adrianzen Fonseca, BS, Kirsten Gunderson, MD, Zeeda Nkana, BS, Aaron Dingle, PhD, Jacqueline Israel, MD, Samuel Poore, MD, PhD
Publikováno v:
Plastic and Reconstructive Surgery, Global Open, Vol 9, Iss 10S, Pp 104-104 (2021)
Externí odkaz:
https://doaj.org/article/d4cf212ba66f470cb9f91dfbc615aa35
Autor:
Scott K. Odorico, Katie Reuter Muñoz, Peter J. Nicksic, Kirsten A. Gunderson, Kasey Wood, Zeeda H. Nkana, Evalina Bond, Samuel O. Poore
Publikováno v:
MicrosurgeryREFERENCES.
Microsurgical free tissue transfer (FTT) is a widely employed surgical modality utilized for reconstruction of a broad range of defects, including head and neck, extremity, and breast. Flap survival is reported to be 90%-95%. When FTT fails, salvage
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac8eb718fb528fa0bad918164767f649
https://pubmed.ncbi.nlm.nih.gov/35611652
https://pubmed.ncbi.nlm.nih.gov/35611652
Publikováno v:
Tetrahedron Letters. 56:1941-1943
A one-step procedure for the synthesis of 4-amidoisoflavans from isoflavanols is described. The synthetic protocol allows for the introduction of a variety of substituents to the isoflavan scaffold via an amide linker.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::826c753e2f7e2cd86b967174e5bd3eeb
https://doi.org/10.1016/j.tetlet.2015.02.072
https://doi.org/10.1016/j.tetlet.2015.02.072
Publikováno v:
Bioorganic & Medicinal Chemistry. 21:1652-1660
Isoflavene–propranolol hybrid molecules were developed as potentially novel anti-tumour agents. Isoflavene itself has potent anti-cancer activity while propranolol can enhance anti-proliferative and anti-angiogenic properties of 5-fluorouracil and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09ef21f3ba6e42f810d5ddf103a3a278
https://doi.org/10.1016/j.bmc.2013.01.059
https://doi.org/10.1016/j.bmc.2013.01.059
Publikováno v:
Tetrahedron. 69:2193-2198
The synthesis of 7-aminoacetylindoles was achieved via the hydrogenation of 7-acylcyanides, which were produced through the oxidation of indole-7-cyanohydrin silylether intermediates. 7-Oxotryptamines were subsequently converted into 5-(7'-indolyl)ox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20465ee090382f34e30bd58495d6fb22
https://doi.org/10.1016/j.tet.2012.12.084
https://doi.org/10.1016/j.tet.2012.12.084
Publikováno v:
Tetrahedron Letters. 53:6697-6700
Oxygenated 4-arylisoflavans and 4-heteroarylisoflavans were synthesized in good yields via BF3·OEt2 catalyzed arylation reactions of 4′,7-diacetoxyisoflavan-4-ol 8 with activated aryl and heteroaryl compounds. These reactions were found to produce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d751bfd675045caa913338e85d8b59d3
https://doi.org/10.1016/j.tetlet.2012.09.117
https://doi.org/10.1016/j.tetlet.2012.09.117
Publikováno v:
Tetrahedron Letters. 52:7095-7098
The activated dimethoxypyrrolo[3,2,1- ij ]quinolin-6-one ring system was synthesized via two approaches, starting from an indole and quinolin-4-one, respectively. Subsequent demethylation led to both monohydroxy- and dihydroxypyrrolo[3,2,1- ij ]quino
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4cf875e9c624251a61b3d0c22a7fad38
https://doi.org/10.1016/j.tetlet.2011.10.089
https://doi.org/10.1016/j.tetlet.2011.10.089
Publikováno v:
Tetrahedron. 67:7603-7610
A range of novel mono- and bis-glyoxylamide peptidomimetics were prepared via the facile ring-opening of N-acylisatins with amino acids and peptide derivatives. The ring-opening of N-acylisatins with dipeptides and tripeptides was discovered to be th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e8ce1e65130053214e905d6f840720b
https://doi.org/10.1016/j.tet.2011.07.036
https://doi.org/10.1016/j.tet.2011.07.036
Publikováno v:
Tetrahedron. 67:4093-4102
A ring closing metathesis approach has been used to prepare a novel range of indoles 1,7-annulated with nitromethyl and lactone functionalised medium-sized rings. Initial studies into the preparation of lactam functionalised rings are also discussed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af0962b2cb23c38fc3393d5a5c7761ec
https://doi.org/10.1016/j.tet.2011.04.019
https://doi.org/10.1016/j.tet.2011.04.019
Publikováno v:
ChemInform. 46
The Ritter reaction of isoflavanol (I) provides a mixture of diastereomers (III) and (IV), independent from whether (I) is applied as a single trans-isomer or as a diastereomeric mixture.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5645d235fb3278eecb34e6ee65dddd5
https://doi.org/10.1002/chin.201530197
https://doi.org/10.1002/chin.201530197