6 research outputs found
Π’Π΅Ρ Π½ΠΎΠ»ΠΎΠ³ΠΈΡΠ΅ΡΠΊΠΈΠ΅ ΡΠ΅ΡΠ΅Π½ΠΈΡ Π΄Π»Ρ ΡΡΡΠΎΠΈΡΠ΅Π»ΡΡΡΠ²Π° ΡΠ°Π·Π²Π΅Π΄ΠΎΡΠ½ΠΎΠΉ Π²Π΅ΡΡΠΈΠΊΠ°Π»ΡΠ½ΠΎΠΉ ΡΠΊΠ²Π°ΠΆΠΈΠ½Ρ Π³Π»ΡΠ±ΠΈΠ½ΠΎΠΉ 3030 ΠΌΠ΅ΡΡΠΎΠ² Π½Π° Π³Π°Π·ΠΎΠ²ΠΎΠΌ ΠΌΠ΅ΡΡΠΎΡΠΎΠΆΠ΄Π΅Π½ΠΈΠΈ (Π’ΡΠΌΠ΅Π½ΡΠΊΠ°Ρ ΠΎΠ±Π»Π°ΡΡΡ)
ΠΠ±ΡΠ΅ΠΊΡΠΎΠΌ ΠΠΠ ΡΠ»ΡΠΆΠΈΡ ΡΠ°Π·Π²Π΅Π΄ΠΎΡΠ½Π°Ρ Π²Π΅ΡΡΠΈΠΊΠ°Π»ΡΠ½Π°Ρ ΡΠΊΠ²Π°ΠΆΠΈΠ½Π° Π³Π»ΡΠ±ΠΈΠ½ΠΎΠΉ 3030 ΠΌΠ΅ΡΡΠΎΠ² Π½Π° Π³Π°Π·ΠΎΠ²ΠΎΠΌ ΠΌΠ΅ΡΡΠΎΡΠΎΠΆΠ΄Π΅Π½ΠΈΠΈ.
Π¦Π΅Π»ΡΡ Π΄Π°Π½Π½ΠΎΠΉ ΡΠ°Π±ΠΎΡΡ ΡΠ²Π»ΡΠ΅ΡΡΡ β ΡΠΏΡΠΎΠ΅ΠΊΡΠΈΡΠΎΠ²Π°ΡΡ ΡΠ΅Ρ
Π½ΠΎΠ»ΠΎΠ³ΠΈΡΠ΅ΡΠΊΠΎΠ΅ ΡΠ΅ΡΠ΅Π½ΠΈΡ Π΄Π»Ρ Π±ΡΡΠ΅Π½ΠΈΡ Π²Π΅ΡΡΠΈΠΊΠ°Π»ΡΠ½ΠΎΠΉ ΡΠ°Π·Π²Π΅Π΄ΠΎΡΠ½ΠΎΠΉ ΡΠΊΠ²Π°ΠΆΠΈΠ½Ρ Π³Π»ΡΠ±ΠΈΠ½ΠΎΠΉ 3030 ΠΌΠ΅ΡΡΠΎΠ² Π½Π° Π³Π°Π·ΠΎΠ²ΠΎΠΌ ΠΌΠ΅ΡΡΠΎΡΠΎΠΆΠ΄Π΅Π½ΠΈΠΈ.
ΠΠ»Ρ Π΄ΠΎΡΡΠΈΠΆΠ΅Π½ΠΈΡ ΠΏΠΎΡΡΠ°Π²Π»Π΅Π½Π½ΠΎΠΉ ΡΠ΅Π»ΠΈ Π±ΡΠ»ΠΈ ΠΏΠΎΡΡΠ°Π²Π»Π΅Π½Ρ ΡΠ»Π΅Π΄ΡΡΡΠΈΠ΅ Π·Π°Π΄Π°ΡΠΈ:
1.Π‘ΠΏΡΠΎΠ΅ΠΊΡΠΈΡΠΎΠ²Π°ΡΡ ΠΊΠΎΠ½ΡΡΡΡΠΊΡΠΈΡ ΡΠΊΠ²Π°ΠΆΠΈΠ½Ρ.
2.Π‘ΠΏΡΠΎΠ΅ΠΊΡΠΈΡΠΎΠ²Π°ΡΡ ΠΏΡΠΎΡΠ΅ΡΡΡ ΡΠ³Π»ΡΠ±Π»Π΅Π½ΠΈΡ ΡΠΊΠ²Π°ΠΆΠΈΠ½Ρ.
3.Π‘ΠΏΡΠΎΠ΅ΠΊΡΠΈΡΠΎΠ²Π°ΡΡ ΠΏΡΠΎΡΠ΅ΡΡΡ Π·Π°ΠΊΠ°Π½ΡΠΈΠ²Π°Π½ΠΈΡ ΡΠΊΠ²Π°ΠΆΠΈΠ½.The object of the WRC is an exploration vertical well with a depth of 30 meters in a gas field.
The purpose of this work is to design a technological solution for drilling a vertical exploration well with a depth of 3030 meters in a gas field.
To achieve this goal, the following tasks were set:
1. Design the well structure.
2. Design the well deepening processes.
3. Design well completion processes
Ru-Catalyzed Isomerization of Achmatowicz Derivatives : A Sustainable Route to Biorenewables and Bioactive Lactones
A Ru-catalyzed isomerization of Achmatowicz derivatives that opens unexplored routes to diversify the biogenic furanic platform is reported. The mechanistic insights of this formally redox-neutral intramolecular process were studied computationally and by deuterium labeling. The transformation proved to be a robust synthetic tool to achieve the synthesis of bioderived-monomers and a series of 4-keto-Ξ΄-valerolactones that further enabled the development of a flexible strategy for the synthesis of acetogenins. A concise and protective group-free asymmetric total synthesis of two natural products, namely, (S,S)-muricatacin and the (S,S)-L-factor, is also described.publishedVersionPeer reviewe