SCOPUS 정보 검색 플랫폼

Volumn 35, Issue 28, 1994, Pages 4967-4968

An improved method of oxazolidinone hydrolysis in the asymmetric synthesis of α-alkylprolines

Author keywords

[No Author keywords available]

Indexed keywords

OXAZOLIDINONE DERIVATIVE; PROLINE DERIVATIVE;

ALKYLATION; AMINO ACID METABOLISM; ARTICLE; CRYSTALLIZATION; FILTRATION; HYDROLYSIS; NONHUMAN; PURIFICATION; STEREOCHEMISTRY;

EID: 0028244615 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(00)73294-1 Document Type: Article

Times cited : (18)

References (15)

1
- 0000093325
- Enantioselective Generation and Diastereoselective Reactions of Chiral Enolates Derived from ?-Heterosubstituted Carboxylic Acids. Preliminary Communication
- (1981) Helvetica Chimica Acta , vol.64 , pp. 2704-2708
- Seebach¹ Naef²

2
- 33845551868
- (1983) J. Am. Chem. Soc. , vol.105 , pp. 5390-5398
- Seebach¹ Boes² Naef³ Schweizer⁴

4
- 0000603109
- (1992) J. Am. Chem. Soc. , vol.114 , pp. 8778-8783
- Genin¹ Johnson²

5
- 0027397579
- (1993) J. Org. Chem. , vol.58 , pp. 860-866
- Genin¹ Gleason² Johnson³

6
- 0001467978
- (1993) J. Org. Chem. , vol.58 , pp. 2334-2337
- Genin¹ Ojala² Gleason³ Johnson⁴

7
- 2542504257
- Design and synthesis of a novel peptide ?-turn mimetic
- (1988) Journal of the Chemical Society, Chemical Communications , pp. 1447-1449
- Hinds¹ Richards² Robinson³

10
- 84913036990
- 2O. The α-alkylated proline product was isolated by filtration as a white solid in high yield.

12
- 84913045875
- 2O in a closed environment often results in additional product crystallization.

13
- 84913026469
- 2O) δ 7.21–7.45 (m, 5 H, Ph), 3.69,4.37 (s, 1 H), 3.43 (d, J = 14.7 Hz, 1 H), 3.01 (d, J = 14.7 Hz, 1 H), 3.32 (t, J = 7.5 Hz, 2 H), 2.41–2.47 (m, 1 H), 1.86–2.16 (m, 3H), 1.01–1.10 (m, 9 H).

15
- 84913034015
- 3OD) δ 3.68 (s, 3 H), 3.46–3.53 (m, 1 H), 3.22–3.32 (m, 1 H), 3.27 (d, J = 17.1 Hz, 1 H), 2.82 (d, J = 17.1 Hz, 1 H), 2.27–2.31 (m, 1 H), 1.89–2.01 (m, 3H).

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.