Synthesis and absolute configuration of the 7-phenylhepta-4,6-diyne-1,2- diol isolated from Bidens pilosa

Synthesis

Volumn , Issue 13, 2011, Pages 2131-2135

  Cui, Shan ^a,b   Zou, Yang ^a   Wu, Yikang ^a   Gao, Po ^b  

^a SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

^b HEILONGJIANG UNIVERSITY   (China)

Author keywords

alcohols; alkynes; coupling; epoxides; natural products

Indexed keywords

ABSOLUTE CONFIGURATION; ACETIC ANHYDRIDES; ALKYNES; CROSS-COUPLINGS; ENANTIOPURE; EPOXIDES; NATURAL PRODUCTS; PHENYLACETYLENES; PROTECTING GROUP; SPECTROSCOPIC DATA; TRIFLATES; TRIMETHYLSILYL;

AROMATIC HYDROCARBONS; CHLORINE COMPOUNDS; NICKEL COMPOUNDS; OPTICAL ROTATION;

ACETYLENE;

1 (BENZYLOXY) 7 PHENYLHEPTA 4,6 DIYN 2 DIOL; 1,2 DIACETYLOXY 5 (6 METHYL 4 OXO 4H PYRAN 2YL)PENT 4 YNE; 6 (6 METHYL 4 OXO 4H PYRAN 2 YL)HEX 5 YNYL ACETATE; 6 (6 METHYL 4 OXO TETRAHYDRO 2H PYRAN 2 YL)HEXYL ACETATE; 7 PHENYLHEPTA 1,2 DIACETYLOXY 4,6 DIYNE; 7 PHENYLHEPTA 4,6 DIYNE 1,2 DIOL; ACETIC ANHYDRIDE; ALKYNE DERIVATIVE; COPPER DERIVATIVE; COPPER IODIDE; NATURAL PRODUCT; NICKEL CHLORIDE; PHENYLACETYLENE; TRIMETHYLSILYL DERIVATIVE; TRIMETHYLSILYLTRIFLATE; UNCLASSIFIED DRUG;

ARTICLE; BIDENS PILOSA; CROSS COUPLING REACTION; DRUG ISOLATION; DRUG STRUCTURE; DRUG SYNTHESIS; ENANTIOSELECTIVITY; NUCLEAR MAGNETIC RESONANCE; PROTON NUCLEAR MAGNETIC RESONANCE; SOLVENT EFFECT;

EID: 80955178404     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0030-1260604     Document Type: Article

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