추천 제품
Quality Level
분석
99%
양식
solid
광학 활성
[α]20/D −67°, c = 3 in chloroform
mp
77-80 °C (lit.)
작용기
hydroxyl
phenyl
SMILES string
OC([C@@H]1CCCN1)(c2ccccc2)c3ccccc3
InChI
1S/C17H19NO/c19-17(16-12-7-13-18-16,14-8-3-1-4-9-14)15-10-5-2-6-11-15/h1-6,8-11,16,18-19H,7,12-13H2/t16-/m0/s1
InChI key
OGCGXUGBDJGFFY-INIZCTEOSA-N
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일반 설명
(S)-(-)-α,α-Diphenyl-2-pyrrolidinemethanol is a bifunctional organocatalyst.
애플리케이션
(S)-(-)-α,α-Diphenyl-2-pyrrolidinemethanol (DPPM) may be used in the following processes:
- DPPM reacts with catecholborane to form a spiroborate ester, which can be an efficient catalyst for the synthesis of enantiopure alcohols by borane reduction of acetophenone.
- The catalyst generated in situ by reacting DPPM with borane-diethylaniline, can efficiently catalyze the enantioselective reduction of 2′-fluoroacetophenone.
- Mesoporous SBA-15 silica functionalized with DPPM can catalyze the addition of diethylzinc to benzaldehyde to form (S)-1-phenyl-propanol.
Used to prepare the corresponding oxazaborolidines for the borane-mediated asymmetric reduction of ketones.
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
Nanoporous silica-supported organocatalyst: a heterogeneous and green hybrid catalyst for organic transformations.
Royal Society of Chemistry Advances, 4(54), 28238-28248 (2014)
Highly enantioselective carbonyl reduction with borane catalyzed by chiral spiroborate esters derived from chiral 1, 2-aminoalcohols.
Tetrahedron Asymmetry, 17(1), 112-115 (2006)
Synlett, 929-929 (1993)
Organic letters, 7(13), 2579-2582 (2005-06-17)
[reaction: see text] An operationally simple and mild protocol for the catalytic enantioselective epoxidation of alpha,beta-unsaturated ketones has been estabilished using commercially available alpha,alpha-diphenyl-l-prolinol as bifunctional organocatalyst and tert-butyl hydroperoxide (TBHP) as oxidant. The epoxides have been obtained in good
The enantioselective reduction of 2'-fluoroacetophenone utilizing a simplified CBS-reduction procedure.
Tetrahedron Asymmetry, 13(13), 1347-1349 (2002)
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