RESUMO
A gold-catalyzed three-component coupling reaction (A3 reaction) was developed as an efficient approach for the synthesis of challenging 2, 4-disubstituted quinoline derivatives. Compared to previously reported Cu/Au bi-catalyst system, this protocol enables achieving A3 reaction only in the presence of triazole-gold catalyst. Notably, 4-alkyl substituted or 2-alkyl substituted quinoline derivatives were obtained with good yields, which highlighted the unique advantage of this new strategy.
RESUMO
Early Cretaceous vertebrate assemblages from East Asia and particularly the Jehol Biota of northeastern China flourished during a period of highly debated climatic history. While the unique characters of these continental faunas have been the subject of various speculations about their biogeographic history, little attention has been paid to their possible climatic causes. Here we address this question using the oxygen isotope composition of apatite phosphate (δ ) from various reptile remains recovered from China, Thailand, and Japan. δ values indicate that cold terrestrial climates prevailed at least in this part of Asia during the Barremian-early Albian interval. Estimated mean air temperatures of about 10 ± 4 °C at midlatitudes (â¼ 42 °N) correspond to present day cool temperate climatic conditions. Such low temperatures are in agreement with previous reports of cold marine temperatures during this part of the Early Cretaceous, as well as with the widespread occurrence of the temperate fossil wood genus Xenoxylon and the absence of thermophilic reptiles such as crocodilians in northeastern China. The unique character of the Jehol Biota is thus not only the result of its evolutionary and biogeographical history but is also due to rather cold local climatic conditions linked to the paleolatitudinal position of northeastern China and global icehouse climates that prevailed during this part of the Early Cretaceous.
Assuntos
Clima Frio , Isótopos de Oxigênio/análise , Animais , Apatitas/química , Ásia , Evolução Biológica , Dinossauros/anatomia & histologia , Fósseis , Fosfatos/químicaRESUMO
A modified continuous-flow elemental analyzer coupled to an isotope-ratio mass spectrometer (modified EA-IRMS) was tested for on-line delta(15)N measurement on urea solution and biological fluids (e.g. urine). The elemental analyzer configuration was adapted by adding a U-shaped cold trap and an X-pattern four-way valve for on-line trapping/venting of water from the liquid samples. Results indicate that the delta(15)N ratios show little variation (standard deviation (SD) = 0.05 per thousand) with a sample size above the equivalent N yield of 0.2 mg urea (0.092 mg N) when the mass spectrometer conditions were carefully optimized. By contrast, a significant logarithmic decrease in delta(15)N with sample size was observed but this can be offset by applying a linearity correction or blank correction when the sample size is between equivalent N yields of 0.05 and 0.2 mg urea. The blank corrected delta(15)N ratios give an overall precision of approximately 0.16 per thousand whereas the average precision for delta(15)N corrected using combined linearity and shift correction is 0.05 per thousand. The relatively large variation in blank corrected delta(15)N values may be attributed to the variability of the blank delta(15)N in the sequence. Therefore, the blank correction should be carefully performed in routine measurements. As a result, the linearity range of a modified EA-IRMS can be extended to a minimum sample size of 0.023 mg N. In addition, the reproducibility of the new system is good, as indicated by the precision (<0.2 per thousand) for a set of standards and unknowns. The data show that fluids containing nitrogen can be successfully analyzed in the modified EA-IRMS.