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Volumn 55, Issue 42, 2014, Pages 5798-5800

A short synthesis of the endogenous plant metabolite 7-hydroxyoxindole-3-acetic acid (7-OH-OxIAA) using simultaneous C-H borylations

Author keywords

7 Hydroxyoxindole 3 acetic acid; 7 OH OxIAA; Auxin; Borylation; C H functionalisation

Indexed keywords

3,4,7,8 TETRAMETHYL 1,10 PHENANTHROLINE; 7 HYDROXYOXINDOLE 3 ACETIC ACID; ANTIOXIDANT; ESTER; INDOLEACETIC ACID DERIVATIVE; IRIDIUM; PHENANTHROLINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84908459848     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2014.08.104     Document Type: Article
Times cited : (21)

References (21)
  • 14
    • 84871908814 scopus 로고    scopus 로고
    • Methyl indole-3-acetate (11) is reasonably priced (25 g = US $150, AK Scientific), but can also be prepared in quantitative yield by Fischer esterification of IAA (100 g = US $60, AK Scientific), see: E. Manzo, D. Pagano, M. Carbone, M.L. Ciavatta, and M. Gavagnin Arkivoc ix 2012 220 228
    • (2012) Arkivoc , vol.9 , pp. 220-228
    • Manzo, E.1    Pagano, D.2    Carbone, M.3    Ciavatta, M.L.4    Gavagnin, M.5
  • 15
    • 77956219116 scopus 로고    scopus 로고
    • The iridium-catalysed diborylation of a tryptophan derivative forms a small quantity of the 2,7-diborylated isomer, with the desired C2-boronate predominating, see: F.-M. Meyer, S. Liras, A. Guzman-Perez, C. Perreault, J. Bian, and K. James Org. Lett. 12 2010 3870 3873
    • (2010) Org. Lett. , vol.12 , pp. 3870-3873
    • Meyer, F.-M.1    Liras, S.2    Guzman-Perez, A.3    Perreault, C.4    Bian, J.5    James, K.6
  • 18
    • 79952450409 scopus 로고    scopus 로고
    • A one-pot borylation-oxidation-hydrolysis has been used to access 3,5-disubstituted phenols, see: A.M. Norberg, M.R. Smith III, and R.E. Maleczka Jr. Synthesis 2011 857 859
    • (2011) Synthesis , pp. 857-859
    • Norberg, A.M.1    Smith, M.R.2    Maleczka, R.E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.