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Tetrahedron Letters

Volumn 25, Issue 39, 1984, Pages 4337-4340

Enantioretentive alkylation of acyclic amino acids

(3) Karady, Sandor a Amto, Joseph S a Weinstock, Leonard M a

a MERCK RESEARCH LABORATORIES (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0000215530 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(01)81432-5 Document Type: Article

Times cited : (110)

References (17)

1
- 13044251079
- The Chemical Society, London
- (1979) Amino Acids, Peptides and Proteins , vol.10 , pp. 11

2
- 0000146414
- Asymmetric Syntheses via Heterocyclic Intermediates; XII1. Enantioselective Synthesis of (R)-α-Amino Acids using tert-Leucine as Chiral Auxiliary Reagent
- (1982) Synthesis , pp. 861
- Schollkopf¹ Neubaer²

3
- 0000093325
- Enantioselective Generation and Diastereoselective Reactions of Chiral Enolates Derived from ?-Heterosubstituted Carboxylic Acids. Preliminary Communication
- (1981) Helvetica Chimica Acta , vol.64 , pp. 2704
- Seebach¹ Naef²

4
- 0000578396
- Synthesis of enantiomerically enriched atrolactic acid and other α-hydroxy acids
- (1981) Tetrahedron Letters , pp. 4221
- Frater¹ Muller² Gunther³

5
- 0000093325
- Enantioselective Generation and Diastereoselective Reactions of Chiral Enolates Derived from ?-Heterosubstituted Carboxylic Acids. Preliminary Communication
- (1981) Helvetica Chimica Acta , vol.64 , pp. 2704
- Seebach¹ Naef²

6
- 33845551868
- (1983) J. Am. Chem. Soc. , vol.105 , pp. 5390
- Seebach¹ Boes² Naef³ Schweizer⁴

7
- 84918380349
- For aldol alkylation of cystein see
- (1983) Tetrahedron Lett. , pp. 315
- Seebach¹ Keber²

8
- 0013469954
- Peptidsynthesen nach dem Oxazolidon-Verfahren, III
- and references therein.
- (1959) Chemische Berichte , vol.92 , pp. 1675
- Michael¹ Meckstroth²

9
- 0002840747
- A recent paper from these laboratories indicated that the major oxazolidinone formed is cis.
- (1983) J. Org. Chew. , vol.48 , pp. 77
- Freidinger¹ Hinkle² Perlow³ Arison⁴

10
- 84918417410
- 3) δ 34.25 (br, C6), 58.16 (C4), 67.69 (C7), 87.1 (br, C2), 151.36 (CON), 170.68 (C5); the broadness of C2 and C6 signals are caused by hindered [[Truncated]]

11
- 84918417409
- 3) δ 17.95 (C6); 52.35 (C4), 68.05 (C7), 86.22 (C2), 153.31 (CON), 171.66 (C5).

12
- 0000852521
- Azomethine Chemistry. II. Formation of Peptides from Oxazolidine-5-ones
- (1962) Journal of the American Chemical Society , vol.85 , pp. 578
- Hiskey¹ Jung²

13
- 84918417408
- Purchased from Callery Chem. Co., Callery PA, as a stable toluene solution.

14
- 84918417407
- 3) δ 23.78 (br, C8), 40.85 (C6), 64.85 [[Truncated]]

15
- 84918417406
- 1H NMR spectrum also indicated a trace of protio compound left.

16
- 84918417405
- 25 + 19.00° (C 0.1, MeOH).

17
- 0015043676
- (1971) J. Med. Chem. , vol.14 , pp. 373
- Bollinger¹

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.