The use of trichioroacetimidate-activated resin for ester formation

Tetrahedron Letters

Volumn 39, Issue 43, 1998, Pages 7959-7962

  Phoon, Chee Wee ^a   Oliver, Steven F ^a   Abell, Chris ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ACETAMIDE DERIVATIVE; ESTER DERIVATIVE; RESIN; THIOL DERIVATIVE;

ARTICLE; CATALYSIS; REACTION ANALYSIS; SYNTHESIS;

EID: 0032558643     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)01729-8     Document Type: Article

References (14)

1. 1. Hermkens, P. H. H.; Ottenheijm, H. J. C.; Rees, D. Tetrahedron 1996, 4527-4554; ibid. 1997, 5643-5678.
2. 1. Hermkens, P. H. H.; Ottenheijm, H. J. C.; Rees, D. Tetrahedron 1996, 4527-4554; ibid. 1997, 5643-5678.
3. 2. Hanessian, S.; Xie, F. Tetrahedron Lett. 1998, 733-736.
4. 3. Patil, V. J. Tetrahedron Lett. 1996, 1481-1484.
5. -1 (m, C-Cl).
6. 5. Nouvet, A.; Lamaty, F.; Lazaro, R. Tetrahedron Lett. 1998, 3469-3470.
7. 6. Kokotos, G.; Chiou, A. Synthesis 1997, 168-170.
8. 2 was used for the other acetic acids. Anhydrous 1,2-dimethoxyethane was used for the benzoic acids.
9. 2 (3 × 5 mL), and dried in vacuo for 48 hours.
10. 9. Eckenberg, P.; Groth, U., Huhn, T.; Richter, N.; Schmeck, C. Tetrahedron 1993, 49, 1619-1629.
11. 10. Recent examples include: Kroll, F. E. K.; Morphy, R.; Rees, D.; Gani, D. Tetrahedron Lett. 1997, 8573-8576; Gayo, L. M.; Suto, M. J. Tetrahedron Lett. 1997, 211-214.
12. 10. Recent examples include: Kroll, F. E. K.; Morphy, R.; Rees, D.; Gani, D. Tetrahedron Lett. 1997, 8573-8576; Gayo, L. M.; Suto, M. J. Tetrahedron Lett. 1997, 211-214.
13. 2 (3 × 10 mL), and dried in vacuo for 48 hours.
14. 2 (3 × 5 mL), and dried in vacuo for 48 hours.