Tags

Type your tag names separated by a space and hit enter

New strategies for the synthesis of biologically important tetrapyrroles. The "B,C + D + A" approach to linear tetrapyrroles.
J Org Chem 2000; 65(1):205-13JO

Abstract

Linear tetrapyrroles related to phytochrome (1) were prepared in enantiospecific fashion by a new strategy beginning with ring-B,C synthons of type 19 (bis-iododipyrrins). Rings A and D were elaborated by Pd(0)-mediated coupling of 19a with the appropriate alkyne acid or amide derivatives 9 and 20, followed by intramolecular cyclization (method C: BC + D + A --> ABCD).

Authors+Show Affiliations

Hall-Atwater Laboratories, Wesleyan University, Middletown, Connecticut 06459-0180, USA.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, U.S. Gov't, P.H.S.

Language

eng

PubMed ID

10813917

Citation

Jacobi, P A., et al. "New Strategies for the Synthesis of Biologically Important Tetrapyrroles. the "B,C + D + A" Approach to Linear Tetrapyrroles." The Journal of Organic Chemistry, vol. 65, no. 1, 2000, pp. 205-13.
Jacobi PA, Coutts LD, Guo J, et al. New strategies for the synthesis of biologically important tetrapyrroles. The "B,C + D + A" approach to linear tetrapyrroles. J Org Chem. 2000;65(1):205-13.
Jacobi, P. A., Coutts, L. D., Guo, J., Hauck, S. I., & Leung, S. H. (2000). New strategies for the synthesis of biologically important tetrapyrroles. The "B,C + D + A" approach to linear tetrapyrroles. The Journal of Organic Chemistry, 65(1), pp. 205-13.
Jacobi PA, et al. New Strategies for the Synthesis of Biologically Important Tetrapyrroles. the "B,C + D + A" Approach to Linear Tetrapyrroles. J Org Chem. 2000 Jan 14;65(1):205-13. PubMed PMID: 10813917.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - New strategies for the synthesis of biologically important tetrapyrroles. The "B,C + D + A" approach to linear tetrapyrroles. AU - Jacobi,P A, AU - Coutts,L D, AU - Guo,J, AU - Hauck,S I, AU - Leung,S H, PY - 2000/5/18/pubmed PY - 2000/10/14/medline PY - 2000/5/18/entrez SP - 205 EP - 13 JF - The Journal of organic chemistry JO - J. Org. Chem. VL - 65 IS - 1 N2 - Linear tetrapyrroles related to phytochrome (1) were prepared in enantiospecific fashion by a new strategy beginning with ring-B,C synthons of type 19 (bis-iododipyrrins). Rings A and D were elaborated by Pd(0)-mediated coupling of 19a with the appropriate alkyne acid or amide derivatives 9 and 20, followed by intramolecular cyclization (method C: BC + D + A --> ABCD). SN - 0022-3263 UR - https://www.unboundmedicine.com/medline/citation/10813917/New_strategies_for_the_synthesis_of_biologically_important_tetrapyrroles__The_"BC_+_D_+_A"_approach_to_linear_tetrapyrroles_ L2 - https://dx.doi.org/10.1021/jo991503u DB - PRIME DP - Unbound Medicine ER -