SCOPUS 정보 검색 플랫폼

Volumn 36, Issue 35, 1995, Pages 6253-6256

Lipase-catalyzed transesterification as a practical route to homochiral acyclic anti-1,2-diols. A new synthesis of (+)- and (-)-endo-brevicomin

Author keywords

[No Author keywords available]

Indexed keywords

BREVICOMIN;

ARTICLE; DRUG SYNTHESIS; ENANTIOMER; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 0029092875 PISSN: 00404039 EISSN: None Source Type: Journal
DOI: 10.1016/0040-4039(95)01237-C Document Type: Article

Times cited : (28)

References (18)

1
- 0002874969
- Readily Available Chiral Carbon Fragments and Their Use in Synthesis
- J.W. Morrison, J.W. Scott, Academic Press, New York
- (1984) Asymmetric Synthesis , vol.4 , pp. 1-226
- Scott¹

2
- 0004106188
- VCH publisher, Weinheim
- (1994) Organic Synthesis , pp. 171-192
- Fuhrhop¹ Penzlin²

3
- 4444276636
- For a recent review, see:
- (1994) Chem. Rev. , vol.94 , pp. 2483-2547
- Wang¹ Sharpless²

4
- 0000797769
- (1992) J. Am. Chem. Soc. , vol.114 , pp. 7568-7570
- Wang¹ Sharpless²

5
- 0347613657
- (1990) J. Am. Chem. Soc. , vol.112 , pp. 4942-4945
- Guo¹ Wu² Chen³ Girdauskas⁴ Sih⁵

7
- 0000296064
- (1992) J. Org. Chem. , vol.57 , pp. 5231-5239
- Wallace¹ Baldwin² Morrow³

9
- 0001532666
- 20 −11.2° (c 4.03, EtOH) for (1R,2S)-enantiomer (77% ee):
- (1993) J. Org. Chem. , vol.58 , pp. 1991-1993
- Hanessian¹ Meffre² Girard³ Beaudoin⁴ Sancean⁵ Bennani⁶

10
- 33751499686
- Similiar rules were proposed previously for the lipase-catalyzed transformations of secondary alcohols and their esters:
- (1991) J. Org. Chem. , vol.56 , pp. 2656-2665
- Kazlauskas¹ Weissfloch² Rapport³ Cuccia⁴

11
- 0007916116
- Pseudomonas lipases as catalysts in organic synthesis: specificity of lipoprotein lipase
- (1992) Journal of the Chemical Society, Chemical Communications , pp. 1411-1413
- Kim¹ Cho²

16
- 84913984365
- The Synthesis of Insect Phermones
- For a review on the synthesis of brevicomin, see:, J. ApSimon, John Wiley and Sons, New York
- (1992) The Total Synthesis of Natural Products
- Mori¹

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.