SCOPUS 정보 검색 플랫폼

Volumn 34, Issue 32, 1993, Pages 5089-5092

A new synthesis of 3-deoxy-d-manno-2-octulosonic acid (KDO)

a CNRS (France)

Author keywords

[No Author keywords available]

Indexed keywords

3 DEOXY MANNO OCTULOSONIC ACID;

ARTICLE; DRUG SYNTHESIS; PRIORITY JOURNAL;

EID: 0027325678 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/S0040-4039(00)60683-4 Document Type: Article

Times cited : (28)

References (19)

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- and references cited therein
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- Dondoni¹ Merion²

3
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- Funktionell substituierte Vinyllithium-Verbindungen, 35. Kurze Synthese von 3-Desoxy-D-manno-2-octulosonsäure (KDO)
- (1989) Liebigs Annalen der Chemie , pp. 69-74
- Enhsen¹ Schmidt²

4
- 0003022332
- A Convenient Synthesis of 3-Deoxy-D-gluco-2-octulosonate (D-gluco-KDO)
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- Lafont¹ Hoch² Schmidt³

6
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- Unger¹

7
- 0000984816
- Other enzymatic attempts that mimic this natural step are described. A last one is, and references cited therein
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- Sugái¹ Shen² Ichikawa³ Wong⁴

8
- 0010508148
- (1989) Tetrahedron Lett. , vol.30 , pp. 5477-5480
- van¹ Boons² Veeneman³ van⁴ van⁵

9
- 0000351344
- A New Synthesis of 3-Deoxy-D-Manno-Octulosonic Acid (KDO) From D-Mannose Via Condensation of Dioxene
- (1989) Journal of Carbohydrate Chemistry , vol.8 , pp. 681-684
- Horito¹ Amano² Hashimoto³

10
- 0023741261
- (1988) Tetrahedron Lett. , vol.38 , pp. 4877-4880
- Ramage¹ Rose²

11
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- (1988) Bull. Chem. Soc. Jpn , vol.61 , pp. 3356-3358
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12
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13
- 0027162845
- An approach based on an aqueous hetero Diels-Alder reaction between a water-soluble dione derived from D-glyceraldehyde and sodium glyoxylate has been recently described:
- (1993) Tetrahedron , vol.49 , pp. 4639
- Lubineau¹ Augé² Lubin³

14
- 37049079232
- Novel application of alkyl dihalogenoacetates; chain extension with an ?-ketoester unit of carbohydrates
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- Coutrot¹ Grison² Tabyaoui³ Czernecki⁴ Valery⁵

15
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- A Convenient Synthesis of α-Keto-esters and Unsymmetrical 1,2-Diketones from Carbonyl Compounds
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17
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18
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- 3) δ 0.10 (s, 3H) ; 0.12 (s, 3H), 0.90 (s, 9H) ; 1.20–1.40 (m, 18H) ; 3.10 (dd, J=8, 17Hz, 1H); 3.22 (dd, J=4, 17Hz, 1H) ; 3.73–3.89 (m, 3H) ; 4.05 (m, 2H); 4.45 (ddd, J=4, 8, 8Hz, 1H); 5.14 (m, J=6.5Hz, 1H).

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.