추천 제품
분석
99%
형태
solid
반응 적합성
core: gadolinium
reagent type: catalyst
mp
>300 °C
SMILES string
CC(C)O[Gd](OC(C)C)OC(C)C
InChI
1S/3C3H7O.Gd/c3*1-3(2)4;/h3*3H,1-2H3;/q3*-1;+3
InChI key
VJLSFXQJAXVOEQ-UHFFFAOYSA-N
애플리케이션
Catalyst for:
- Enantioselective construction of beta-quaternary carbons via conjugate addition reactions
- Generation of reactive enolates
- Regioselective / stereoselective conjugate addition of cyanide to enones
- Strecker reactions
- Asymmetric ring-opening of meso-aziridines
Catalyst used in a ring opening of meso-aziridines with trimethylsilyl azide.
In many asymmetric catalysis applications, glove box and Schlenk techniques should be employed to prevent exposure of the rare earth catalyst to air and moisture, which can be detrimental to the reaction outcome. Solutions of the catalyst should be made using anhydrous solvents and used shortly after preparation.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
Journal of the American Chemical Society, 128(19), 6312-6313 (2006-05-11)
An asymmetric ring-opening reaction of meso-aziridines with TMSN3 was developed using a catalyst prepared from Y(OiPr)3 and chiral ligand 2 in a 1:2 ratio. Excellent enantioselectivity was realized from a wide range of substrates with a practical catalyst loading. The
관련 콘텐츠
Professor Shibasaki's research focuses on the development of novel cooperative asymmetric catalytic systems that allowed for streamlined synthesis of enantioenriched high-value chiral building blocks.
자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..
고객지원팀으로 연락바랍니다.