Synthesis of γ-monofluorinated goniothalamin analogues via regio- and stereoselective ring-opening hydrofluorination of epoxide

Journal of Organic Chemistry

Volumn 76, Issue 16, 2011, Pages 6525-6533

  Chen, Jun Ling ^a   Zheng, Feng ^b   Huang, Yangen ^a   Qing, Feng Ling ^a,b  

^a DONGHUA UNIVERSITY   (China)

^b SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ALLYL ALCOHOLS; BUILDING BLOCKES; GONIOTHALAMIN; REGIOSELECTIVE REDUCTION; RING OPENING; SHARPLESS EPOXIDATION; STEREO-SELECTIVE; STEREOSELECTIVE SYNTHESIS;

STEREOCHEMISTRY; STEREOSELECTIVITY; SYNTHESIS (CHEMICAL);

REGIOSELECTIVITY;

(4,5) 6 (BENZYLOXY) 4 FLUOROHEX 2 YNE 1,5 DIOL; (5,6) 5 FLUORO 5,6 DIHYDRO 6 STYRYLPYRAN 2 ONE; 3 [(2,3) 3 [(BENZYLOXY)METHYL]OXIRAN 2 YL]PROP 2 YN 1 OL; 6 (TERT BUTYLDIMETHYLSILYLOXY)HEX 2 EN 4 YN 1 OL; 6 (TERT BUTYLDIMETHYLSILYLOXY)HEXA 2,4 DIYN 1 OL; EPOXIDE; FLUOROHYDRIN; LACTONE DERIVATIVE; PYRAN DERIVATIVE; TERAZOSIN; UNCLASSIFIED DRUG;

ARTICLE; CHEMISTRY; CHIRALITY; CYCLIZATION; DRUG STRUCTURE; DRUG SYNTHESIS; ELECTRON; FLUORINATION; FLUORINE NUCLEAR MAGNETIC RESONANCE; HYDROFLUORINATION; OXIDATION; REDUCTION KINETICS; REGIOSELECTIVITY; RING OPENING; SHARPLESS EPOXIDATION; STEREOCHEMISTRY;

EPOXY COMPOUNDS; HYDROCARBONS, FLUORINATED; LACTONES; MOLECULAR STRUCTURE; PYRONES; STEREOISOMERISM;

EID: 80051712408     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo200611w     Document Type: Article

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