Functionalized pinols: 13C and 1H NMR spectra assignments and structures

Spectroscopy Letters

Volumn 34, Issue 3, 2001, Pages 387-394

  Kaiser, Carlos R ^a   Da Silva, Flavia M ^a   Jones Jr , Joel ^a   De Mattos, Marcio C S ^a  

^a FEDERAL UNIVERSITY OF RIO DE JANEIRO   (Brazil)

Author keywords

13C Pendant; 1H and 13CNMR; 1H spectra simulations; COSY 45; COSY DQF; Functionalized pinols; HMBC; HMQC; NOESY

Indexed keywords

2,6 DIMETHYL 6 IODOMETHYL 7 OXABICYCLO[3.2.1]OCT 2 ENE; 2,6,6 TRIMETHYL 7 OXABICYCLO[3.2.1]OCTAN 2 OL; ALKENE DERIVATIVE; CARVEOL; TERPENOID DERIVATIVE; TERPINEOL; UNCLASSIFIED DRUG;

AQUEOUS SOLUTION; ARTICLE; CALCULATION; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL STRUCTURE; HALOGENATION; MATHEMATICAL ANALYSIS; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; SIMULATION; STRUCTURE ANALYSIS;

EID: 0035745031     PISSN: 00387010     EISSN: None     Source Type: Journal    
DOI: 10.1081/SL-100002294     Document Type: Article

References (11)

1. Cohalogenation in organic synthesis
2. Organic halides
3. An easy and efficient synthesis of iodohydrins from alkenes
4. 2
5. Unsymmetrical ketone synthesis via a three-component connection reaction of organozincs, allylating agents carbon monoxide
6. Halogenated terpenoids. XX the seven monochlorocineoles
7. NMR assignments for some 2-substituted 2,6,6-trimethyl-7-oxa-bicyclo[3.2.1]octanes (dihydropinols)
8. Long-range proton spin-spin coupling
9. New method for NMR signal enhancement by polarization transfer, and attached nucleus testing