Phorboxazole B Synthetic Studies: Construction of C(1?32) and C(33?46) Subtargets.

Ian Paterson; Alan Steven; Chris A. Luckhurst

doi:10.1002/chin.200512239

Phorboxazole B Synthetic Studies: Construction of C(1?32) and C(33?46) Subtargets.

ChemInform ◽

10.1002/chin.200512239 ◽

2005 ◽

Vol 36 (12) ◽

Author(s):

Ian Paterson ◽

Alan Steven ◽

Chris A. Luckhurst

Keyword(s):

Phorboxazole B ◽

Synthetic Studies

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Synthetic Studies Towards Phorboxazole B: Stereoselective Synthesis of the C3-C19 Bis-oxane Oxazole Fragment

Synlett ◽

10.1055/s-2003-41462 ◽

2003 ◽

pp. 1817-1821

Author(s):

Wei-shan Zhou ◽

Dong-hui Zhang

Keyword(s):

Stereoselective Synthesis ◽

Phorboxazole B ◽

Synthetic Studies

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Phorboxazole B synthetic studies: construction of C(1–32) and C(33–46) subtargets

Organic & Biomolecular Chemistry ◽

10.1039/b407240e ◽

2004 ◽

Vol 2 (20) ◽

pp. 3026-3038 ◽

Cited By ~ 36

Author(s):

Ian Paterson ◽

Alan Steven ◽

Chris A. Luckhurst

Keyword(s):

Phorboxazole B ◽

Synthetic Studies

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Synthetic Studies Towards Phorboxazole B: Stereoselective Synthesis of the C3—C19 Bis-oxane Oxazole Fragment.

ChemInform ◽

10.1002/chin.200408250 ◽

2004 ◽

Vol 35 (8) ◽

Author(s):

Dong-hui Zhang ◽

Wei-shan Zhou

Keyword(s):

Stereoselective Synthesis ◽

Phorboxazole B ◽

Synthetic Studies

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Synthetic studies toward inducamide C

Organic & Biomolecular Chemistry ◽

10.1039/d0ob01995j ◽

2021 ◽

Author(s):

Ardalan A. Nabi ◽

Lydia M. Scott ◽

Daniel P. Furkert ◽

Jonathan Sperry

Keyword(s):

Natural Product ◽

Structural Revision ◽

Synthetic Studies

The rare benzoxazepine ring in the alkaloid inducamide C is unstable and prone to rearrangement, indicating that structural revision of the natural product may be necessary.

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Synthetic studies towards the antiviral pyrazine derivative T-705

10.3390/ecsoc-13-00223 ◽

2009 ◽

Author(s):

Ulrich Jordis ◽

Sagar Beldar

Keyword(s):

Pyrazine Derivative ◽

Synthetic Studies

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Synthetic studies on the preparation of dinucleoside phenylphosphonates and phenylphosphonothioates via palladium(0) catalysed cross-coupling

Collection Symposium Series ◽

10.1135/css200507195 ◽

2005 ◽

Cited By ~ 4

Author(s):

Gaston Lavén ◽

Jacek Stawinski

Keyword(s):

Cross Coupling ◽

Synthetic Studies

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Synthetic studies on the P–C bond formation via a palladium-catalyzed cross-coupling reaction. Application to the synthesis of P-arylated nucleic acids

Collection Symposium Series ◽

10.1135/css200810214 ◽

2008 ◽

Cited By ~ 3

Author(s):

Marcin Kalek ◽

Jacek Stawinski

Keyword(s):

Nucleic Acids ◽

Bond Formation ◽

Coupling Reaction ◽

Cross Coupling ◽

Cross Coupling Reaction ◽

Palladium Catalyzed ◽

Synthetic Studies

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ChemInform Abstract: SYNTHETIC STUDIES IN THE ALKALOID FIELD PART 2, ON THE PREPARATION OF N-(BETA-INDOLYLETHYL)-DIHYDRO- AND N-(BETA-INDOLYLETHYL)-TETRAHYDROPYRIDINES BY CATALYTIC HYDROGENATION, AND THEIR ACID-INDUCED CYCLIZATION

Chemischer Informationsdienst ◽

10.1002/chin.197549297 ◽

1975 ◽

Vol 6 (49) ◽

pp. no-no

Author(s):

MAURI LOUNASMAA ◽

CARL-JOHAN JOHANSSON

Keyword(s):

Catalytic Hydrogenation ◽

Synthetic Studies

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ChemInform Abstract: SYNTHETIC STUDIES ON OPTICALLY ACTIVE β-LACTAMS. CHIRAL SYNTHESIS OF CARBAPENAM RING SYSTEM STARTING FROM L-ASPARTIC ACID

Chemischer Informationsdienst ◽

10.1002/chin.198101209 ◽

1981 ◽

Vol 12 (1) ◽

Author(s):

N. IKOTA ◽

H. SHIBATA ◽

K. KOGA

Keyword(s):

Aspartic Acid ◽

Ring System ◽

Optically Active ◽

Chiral Synthesis ◽

Synthetic Studies

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ChemInform Abstract: SYNTHETIC STUDIES ON OPTICALLY ACTIVE EPOXYTERPENES FROM L-GLUTAMIC ACID. II. YNTHESES OF R-(+)-10,11-EPOXYFARNESOL, R-(+)-, AND S-(-)-SQUALENE-2,3-OXIDE

Chemischer Informationsdienst ◽

10.1002/chin.197642363 ◽

1976 ◽

Vol 7 (42) ◽

pp. no-no

Author(s):

S. YAMADA ◽

N. OH-HASHI ◽

K. ACHIWA

Keyword(s):

Glutamic Acid ◽

Optically Active ◽

Synthetic Studies

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