Attainment of syn-selectivity for boron-mediated asymmetric aldol reactions of carboxylic esters

Tetrahedron Letters

Volumn 39, Issue 14, 1998, Pages 1873-1876

  Liu, Ji Feng ^a   Abiko, Atsushi ^b   Pei, Zhonghua ^a,c   Buske, Dana C ^a   Masamune, Satoru ^a  

^a MASSACHUSETTS INSTITUTE OF TECHNOLOGY   (United States)

^b KYOTO INSTITUTE OF TECHNOLOGY   (Japan)

^c ABBOTT LABORATORIES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; ESTER; MACROLIDE; NATURAL PRODUCT; REAGENT; TEDANOLIDE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; ENANTIOMER; REACTION ANALYSIS; STEREOCHEMISTRY; SYNTHESIS;

EID: 0032473863     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)00123-3     Document Type: Article

References (12)

1. 3. For example, see (a) Kirn, B.-M.; Williams, S. F.; Masamune, S. Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, 1991; Vol. 2 (Heathcock, C. H., Ed), Chapter 1.7, p 239.
2. (b) Heathcock, C. H. Modern Synthetic Methods; Scheffold, R., Ed.; VCH: New York, 1992; p 1.
3. (c) Braun, M.; Sacha,; H. J. Prakt. Chem. 1993, 335, 653.
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6. 6. Both enantiomers are available from Aldrich.
7. 7. 1,2,3,4,6,7,8,9-octahydroanthracenesulfonyl chloride (3) was prepared from 1,2,3,4,6,7,8,9-octahydroanthracene by the literature method. Schroeter, G. Chem. Ber. 1924, 57, 2003.
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11. (b) Fusetani, N.; Matsunaga, S. J. Org. Chem. 1991, 56, 4971.
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