추천 제품
product name
L-tert-Leucine, 99%
Quality Level
분석
99%
형태
powder
광학 활성
[α]20/D −9.5°, c = 3 in H2O
광학 순도
ee: 99% (GLC)
반응 적합성
reaction type: solution phase peptide synthesis
mp
≥300 °C (lit.)
응용 분야
peptide synthesis
SMILES string
CC(C)(C)[C@H](N)C(O)=O
InChI
1S/C6H13NO2/c1-6(2,3)4(7)5(8)9/h4H,7H2,1-3H3,(H,8,9)/t4-/m1/s1
InChI key
NPDBDJFLKKQMCM-SCSAIBSYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
L-tert-Leucine is an amino acid used as a precursor for synthesizing chiral tridentate Schiff base ligands.
애플리케이션
L-tert-Leucine can be used:
- As a key precursor in the synthesis of a chiral phosphinooxazoline ligand, (S)-tert-butylPHOX.
- In the synthesis of chiral copper(II) polymers that can catalyze the kinetic resolution of secondary alcohols by acylation.
- In metal-free tandem radical cyclization reactions to synthesize 6-alkyl/acyl phenanthridines.
- In the preparation of tert-leucine-derived N-acetylthiazolidinethione auxiliary that provides high levels of diastereoselection in acetate aldol reactions with a variety of aldehydes.
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
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.
Synthesis, structure and application of chiral copper (II) coordination polymers for asymmetric acylation.
Inorganic Chemistry, 47(12), 5093-5098 (2008)
Tridentate ligands derived from L-tert-Leucine for the Cu (II) mediated asymmetric Henry reaction
Turkish Journal of Chemistry, 35, 361-374 (2011)
Highly Selective Asymmetric Acetate Aldol Reactions of an N-Acetyl Thiazolidinethione Reagent.
Organic Letters, 6(1), 23-25 (2004)
Preparation of (S)?tert?Butyl PHOX: (Oxazole, 4?(1, 1?Dimethylethyl)?2?[2?(Diphenylphosphino) Phenyl]?4, 5?Dihydro?(4S)?).
Organic Syntheses, 86, 181-193 (2003)
Use of unprotected amino acids in metal-free tandem radical cyclization reactions: divergent synthesis of 6-alkyl/acyl phenanthridines.
Royal Society of Chemistry Advances, 7(88), 55891-55896 (2017)
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