Ligand-Free Palladium-Catalyzed Oxyarylation of Dihydronaphthal­enes and Chromenequinone with o-Iodophenols and 3-Iodolawsone in PEG-400: An Efficient Synthesis of 5-Carbapterocarpans and Pterocarpanquinones

Dihydronaphthalenes were oxyarylated with o-iodophenols, in PEG-400 at 140 or 170 °C, leading regio- and stereoselectively to 5-carbapterocarpans. By using Pd(OAc)2 (5–10 mol%) as precatalyst and Ag2CO3 (1.1 equiv) as base (conditions A), products were obtained in good to excellent chemical yields, in 5–30 minutes, irrespective of the pattern of substitution the starting materials. Alternatively, when p-hydroxyacetophenone oxime derived palladacycle (1 mol%) was used as precatalyst, and dicyclohexylamine (2 equiv) was used as base (silver-free, conditions B), the corresponding adducts were obtained in moderate to good yields, in 0.5 to 4 hours. Finally, the oxyarylation of dihydronaphthalenes­ and chromenquinone with o-iodophenols and 3-iodolawsone in PEG-400 under conditions A led regio- and stereoselectively to the formation of carbapterocarpanquinones and pterocarpanquinones in moderate yield.Financial support from Brazilian agencies CAPES-DGU (Project 200/09), CNPq, FAPERJ and UFRJ are acknowledged. Spanish MICINN (Projects PHB2008-0037-PC, CTQ2007-62771/BQU, CTQ2010-20387, Consolider INGENIO 2010 CSD2007-00006), FEDER, Generalitat Valenciana (Project PROMETEO/2009/038), and the University of Alicante are acknowledged

Cryopreservation of caprine ovarian tissue using glycerol and ethylene glycol

Cryopreservation of ovarian tissue may be a potential alternative for the conservation of genetically superior animals, including high milk- and meat-producing goat breeds. However, until now, no information was available concerning the cryopreservation of preantral follicles (PF) enclosed in caprine ovarian tissue. The objective of the present study was to evaluate the structural and ultrastructural characteristics of caprine PF after exposure to and cryopreservation of ovarian tissue in 1.5 and 3 M glycerol (GLY) and ethylene glycol (EG). At the slaughterhouse, each ovarian pair from five adult mixed breed goats was divided into nine fragments and randomly distributed into treatment groups. One fragment was immediately fixed for histological examination and ultrastructural analysis, after slaughter (control). Four of the ovarian fragments were equilibrated at 20 °C for 20 min in 1.8 ml of MEM containing 1.5 or 3 M GLY or EG for a toxicity test and the final four fragments were slowly frozen using these cryoprotectants at the concentrations above. After toxicity testing and freezing/thawing, the ovarian fragments were fixed for histological examination. Histological analysis showed that after toxicity testing and cryopreservation of the ovarian tissue in GLY or EG at both concentrations, the percentage of normal PF was significantly lower than controls. Ultrastructural analysis of PF frozen in 1.5 and 3 M GLY, as well as 3 M EG demonstrated that these follicles remained morphologically normal. In conclusion, we demonstrated cryopreservation of caprine PF in ovarian tissue

Degeneration rate of preantral follicles in the ovaries of goats

The degeneration rate of ovarian preantral follicles in goats, and the distribution in the follicular classes (primordial, primary or secondary) was assessed. Ovaries from adult goats were collected at a local slaughterhouse. To evaluate the morphology of the caprine preantral follicles in situ, one fragment from each ovary was fixed individually in Carnoy for 12 h, sectioned serially at a thickness of 7 μm and stained with Periodic Acid Shiff-hematoxylin. Preantral follicles were then classified according to the stage of development. Preantral follicles were classified individually either as morphologically normal; as Type 1 degenerated follicles (only the oocyte was degenerated); or as Type 2 degenerated follicles (when degeneration occurred at both oocyte and granulosa cells). The total examined was 235 primordial, 195 primary and 101 secondary follicles. The distribution of degenerated follicles as primordial, primary and secondary follicles was 8.5, 14.3 and 16.8%, respectively. When Types 1 and 2 degenerated follicles were pooled, secondary follicles were significantly more degenerated than primordial and primary follicles. When degeneration Types 1 and 2 was compared in each follicular class, a higher (P<0.05) percentage of Type 1 degeneration was observed in primordial and primary follicles. Conversely, secondary follicles were significantly more affected by Type 2 degeneration. When the follicular classes were taken together, a significantly higher percentage of Type 1 degenerated preantral follicles was observed when compared with Type 2 degenerated follicles (P<0.05). In conclusion, a low percentage of degenerated preantral follicles was observed and secondary follicles were more affected by degeneration than primordial follicles. Thus, primordial follicles constitute a large and potentially valuable source of oocytes for reproductive programs after in vitro growth and maturation

Mesons and baryons in a soft-wall holographic approach

We discuss a holographic soft-wall model developed for the description of mesons and baryons with adjustable quantum numbers n, J, L, S. This approach is based on an action which describes hadrons with broken conformal invariance and which incorporates confinement through the presence of a background dilaton field.Comment: 6 pages, Presented by Valery E. Lyubovitskij at LIGHTCONE 2011, 23 - 27 May, 2011, Dalla