Biomimetic synthesis of (-)-Xestospongin A, (+)-Xestospongin C, (+)-Araguspongine B and the correction of their absolute configurations

Biomimetic synthesis of (-)-Xestospongin A, (+)-Xestospongin C, (+)-Araguspongine B and the correction of their absolute configurations

Detalles Bibliográficos
Main Authors:	Baldwin, J, Melman, A, Lee, V, Firkin, C, Whitehead, R
Formato:	Journal article
Idioma:	English
Publicado:	1998

Títulos similares

Isolation of Araguspongine M, a New Stereoisomer of an Araguspongine/Xestospongin alkaloid, and Dopamine from the Marine Sponge Neopetrosia exigua Collected in Palau
por: Xinsheng Yao, et al.
Publicado: (2004-11-01)

Biomimetic synthesis of marine sponge metabolite spiculoic acid A and establishment of the absolute configuration of the natural product.
por: Kirkham, J, et al.
Publicado: (2006)

Synthesis of marine sponge alkaloid hachijodine B and a comment on the structure of ikimine B and on the absolute configuration of niphatesine D
por: Romeril, S, et al.
Publicado: (2004)

Studies on the biomimetic synthesis of the manzamine alkaloids
por: Baldwin, J, et al.
Publicado: (1999)

STUDIES TOWARDS A BIOMIMETIC SYNTHESIS OF THE MANZAMINES
por: Baldwin, J, et al.
Publicado: (1995)

Araguspongine C Induces Autophagic Death in Breast Cancer Cells through Suppression of c-Met and HER2 Receptor Tyrosine Kinase Signaling
por: Mohamed R. Akl, et al.
Publicado: (2015-01-01)

Total Synthesis of Gobiusxanthin Stereoisomers and Their Application to Determination of Absolute Configurations of Natural Products: Revision of Reported Absolute Configuration of Epigobiusxanthin
por: Yumiko Yamano, et al.
Publicado: (2014-12-01)

Total Synthesis and Absolute Configuration of the Marine Norditerpenoid Xestenone
por: Hiroaki Miyaoka, et al.
Publicado: (2009-11-01)

Total synthesis of polycephalin C and determination of the absolute configurations at the 3",4" ring junction.
por: Longbottom, D, et al.
Publicado: (2002)

The absolute configuration of curcumalactone /
por: Gao, Ji-Fu

Synthesis of an advanced C10-C32 spiroacetal fragment and assignment of the absolute configuration of spirangien A.
por: Paterson, I, et al.
Publicado: (2007)

(-)-Pseudodistomin E: First asymmetric synthesis and absolute configuration assignment
por: Davies, S, et al.
Publicado: (2017)

The absolute configuration and conformation of neocurdione /
por: Tamiko Ohkura

3-Nitroatenolol: First Synthesis, Chiral Resolution and Enantiomers’ Absolute Configuration
por: Rosa Sparaco, et al.
Publicado: (2024-04-01)

Biomimetic synthesis of the crispatene core.
por: Moses, J, et al.
Publicado: (2003)

A BIOMIMETIC APPROACH TO THE MANZAMINE ALKALOIDS
por: Baldwin, J, et al.
Publicado: (1995)

A biomimetic approach to the manzamine alkaloids
por: Spring, DR, et al.
Publicado: (1997)

Biomimetic synthesis of (+/-)-9,10-deoxytridachione.
por: Moses, J, et al.
Publicado: (2005)

A BIOMIMETIC APPROACH TO THE MANZAMINE ALKALOIDS - MODEL STUDIES
por: Baldwin, J, et al.
Publicado: (1994)

The absolute configuration of 1-epialexine hemihydrate.
por: Thompson, A, et al.
Publicado: (2008)

Synthesis, Chiral Resolution and Enantiomers Absolute Configuration of 4-Nitropropranolol and 7-Nitropropranolol
por: Rosa Sparaco, et al.
Publicado: (2022-12-01)

Asymmetric Synthesis and Absolute Configuration Assignment of a New Type of Bedaquiline Analogue
por: Chang-Jiang Qiao, et al.
Publicado: (2015-12-01)

A biomimetic approach to the manzamine alkaloids
por: Baldwin, J, et al.
Publicado: (1996)

A short biomimetic synthesis of the meroterpenoids guajadial and psidial A.
por: Lawrence, A, et al.
Publicado: (2010)

Optically pure trans-1-benzyl-4-aminopiperidin-3-ols. Synthesis and absolute configuration
por: Galina V. Grishina, et al.
Publicado: (2011-07-01)

Levetiracetam analogs: chemoenzymatic synthesis, absolute configuration assignment and evaluation of cholinesterase inhibitory activities
por: Cintia Duarte de Freitas Milagre, et al.
Publicado: (2022-04-01)

Levetiracetam analogs: chemoenzymatic synthesis, absolute configuration assignment and evaluation of cholinesterase inhibitory activities
por: Cintia Duarte de Freitas Milagre, et al.
Publicado: (2022-04-01)

Atlas of stereochemistry : absolute configurations of organic molecules/
por: 244867 Klyne, William, et al.
Publicado: (1978)

Absolute Configuration of In Situ Crystallized (+)-γ-Decalactone
por: Michael Patzer, et al.
Publicado: (2021-04-01)

On the absolute stereochemistry of pyrinodemin A.
por: Romeril, S, et al.
Publicado: (2003)

(-)-(2S,3R,Z)-Nakinadine A: first asymmetric synthesis and absolute configuration assignment.
por: Davies, S, et al.
Publicado: (2014)

Synthesis, Absolute Configuration, Biological Profile and Antiproliferative Activity of New 3,5-Disubstituted Hydantoins
por: Mladenka Jurin, et al.
Publicado: (2024-09-01)

Microwave-Assisted Synthesis of (±)-Mandelic Acid-d5, Optical Resolution, and Absolute Configuration Determination
por: Claudio Bruno, et al.
Publicado: (2013-01-01)

Asymmetric synthesis of aldol products derived from unsymmetrical ketones: assignment of the absolute configuration of antibody aldol products
por: Maggiotti, V, et al.
Publicado: (2002)

Synthesis, structure revision, and absolute configuration of (+)-didemniserinolipid B, a serinol marine natural product from a tunicate Didemnum sp.
por: Kiyota, H, et al.
Publicado: (2002)

The reflection invariance problems in stereochemical nomenclature for absolute configuration
por: Bhattacharya Prabuddha, et al.
Publicado: (2023-05-01)

Enantiomeric Resolution and Absolute Configuration of a Chiral δ-Lactam, Useful Intermediate for the Synthesis of Bioactive Compounds
por: Roberta Listro, et al.
Publicado: (2020-12-01)

Absolute C++ /
por: 233936 Savitch, Walter
Publicado: (2006)

Chromatographic methods in the determination of absolute and relative configurations of fatty acids /
por: 451759 Smith, C. R.

A Revised Structure and Assigned Absolute Configuration of Theissenolactone A
por: Melissa M. Cadelis, et al.
Publicado: (2020-10-01)