STEREOCHEMICAL STUDIES ON BORONOLIDE, AN α-PYRONE FROM TETRADENIA BARBERAE

DOI: 10.1016/S0031-9422(00)84590-2

Source and publish data:

Phytochemistry p. 3047 - 3050 (1987)

Update date:2022-08-29

Topics:

Authors:

Davies-Coleman, Michael T.

Rivett, Douglas E. A.

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/S0031-9422(00)84590-2

Key Word Index-Tetradenia barberae; Lamiaceae; α-pyrone; boronolide. The structure of boronolide isolated from Tetradenia barberae has been confirmed as 6R-<1R,2R,3S-(trisacetyloxy)-heptyl>-5,6-dihydro-2H-pyran-2-one by chemical degradation.

Full text of DOI:10.1016/S0031-9422(00)84590-2

Products guided by the article

Product name:D(+)-Malic acid

Cas No:636-61-3

R&D Labs maybe for 636-61-3

Shanghai Yurui Biotechnology(Anyang) Pharmaceutical Co., Ltd

Contact:+86-0372-3662335 +86-0372-3661988

Address:hanling industrial park anyang
Jinhua Haoyuan Chemical CO., LTD(expird)

Contact:86-579-82465583

Address:Jinhua,Zhejiang
Anhui Eapearl Chemical Co., Ltd.

Contact:86-562-5858458

Address:358 South Huaihe Road
Changsha Easchem Co.,Limited

website:http://www.easchem.com

Contact:+86-731-89722861 89722891

Address:2/F-4/Bld Colorful Palace, No.605 Changsha Ave, Yuhua Area Changsha Hunan China.
Longhui qunfeng Chemical Co., Ltd

Contact:86-731-82173407

Address:South-east Industrial Park, Longhui County, Hunan Province, China

Relevant to this article

Selective two-step labeling of proteins with an off/on fluorescent probe

Doi:10.1002/chem.201102664
(2011)
Effect of isotopic substitution on the electron spin dynamics of the CH₃C(COOH)₂ radical in X-irradiated methyl malonic acid powder: Intrinsic potentials and activation energies

Doi:10.1021/jp972067n
(1997)
Isolation of an oxomanganese(v) porphyrin intermediate in the reaction of a manganese(III) porphyrin complex and H₂O₂ in aqueous solution

Doi:10.1002/1521-3765(20020503)8:9<2067::AID-CHEM2067>3.0.CO;2-V
(2002)
Reactions of vinyldisilanes with ruthenium carbonyl

Doi:10.1246/cl.1999.717
(1999)
Doi:10.1063/1.1700651
(1952)
Discovery of EGF Receptor Inhibitors That Are Selective for the d746-750/T790M/C797S Mutant through Structure-Based de Novo Design

Doi:10.1002/anie.201703389
(2017)

Article Doi