SCOPUS 정보 검색 플랫폼

Volumn 5, Issue 4, 1994, Pages 723-730

Asymmetric epoxidation using chiral sulfur ylides

Author keywords

[No Author keywords available]

Indexed keywords

PINENE DERIVATIVE; SULFIDE; UNCLASSIFIED DRUG;

ARTICLE; DRUG SYNTHESIS; PRIORITY JOURNAL; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 0028205087 PISSN: 09574166 EISSN: 1362511X Source Type: Journal
DOI: 10.1016/0957-4166(94)80035-9 Document Type: Article

Times cited : (43)

References (25)

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10
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- Furukawa¹ Sugihara² Fujihara³

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14
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- Solladie-Cavallo¹ Adib²

15
- 84908839931
- The enantiomeric excess of (+)-isopinocampheol was 〉 95% ee as determined by chiral GC. It was not possible to independently determine the enantiomeric excesses of the correponding thiol or sulfides by chiral GC, HPLC, or NMR.

20
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- (1986) Synthetic Communications , vol.16 , pp. 611-616
- Rollin¹

24
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- B.M. Trost, I. Fleming, Pergamon, Oxford
- (1991) Comprehensive Organic Synthesis , vol.3 , pp. 913-974
- Markó¹

25
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- (1976) Tetrahedron , vol.32 , pp. 2071
- Dansette¹ Ziffer² Jerina³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.