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[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10](=[O:24])[CH2:11][CH2:12][C:13]([C:15]2[CH:20]=[CH:19][C:18]([N+:21]([O-:23])=[O:22])=[CH:17][CH:16]=2)=[O:14])=[CH:6][CH:5]=1)([O-:3])=[O:2].C1(C(C2C=CC=CC=2)([C@@H]2CCCN2)O)C=CC=CC=1>>[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C@@H:10]([OH:24])[CH2:11][CH2:12][C@@H:13]([C:15]2[CH:20]=[CH:19][C:18]([N+:21]([O-:23])=[O:22])=[CH:17][CH:16]=2)[OH:14])=[CH:6][CH:5]=1)([O-:3])=[O:2]참가 물질
3
실험 절차
The product from Example 1A (30 g, 95 wt %, 91.4 mmol) was subjected to the conditions described in Example 32, substituting (R)-(−)-α,α-diphenyl-2-pyrrolidinemethanol for (S)-(−)-α,α-diphenyl-2-pyrrolidinemethanol, to give the title compound (20.14 g, >99.55 ee, 61% yield) which was contaminated with 9.7% of the meso isomer (vs. dl isomer).
출처 및 근거
- ORD 기록
- ord-6063b9267a044a2fb3df49b0fce5ba8b
- 출처 데이터셋
- uspto-grants-2014_04
- 특허 번호
- US08691938B2
연결된 노트
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