Indole Prenylation in Alkaloid Synthesis

Topics in Current Chemistry - Alkaloid Synthesis ◽

10.1007/128_2011_204 ◽

2011 ◽

pp. 67-129 ◽

Cited By ~ 52

Author(s):

Thomas Lindel ◽

Nils Marsch ◽

Santosh Kumar Adla

Keyword(s):

Alkaloid Synthesis

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Free radical cyclizations in alkaloid synthesis: (+)-heliotridine and (+)-hastanecine

Tetrahedron ◽

10.1016/s0040-4020(01)97176-5 ◽

1985 ◽

Vol 41 (19) ◽

pp. 3959-3971 ◽

Cited By ~ 72

Author(s):

Joong-Kwon Choi ◽

David J. Hart

Keyword(s):

Free Radical ◽

Radical Cyclizations ◽

Alkaloid Synthesis ◽

Free Radical Cyclizations

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ChemInform Abstract: Methods for Indole Alkaloid Synthesis. Enantiospecific Synthesis of Pentacyclic Desethylaspidosperma-Type Alkaloids Using an Exceptionally Mild Retro-Diels-Alder Reaction.

Chemischer Informationsdienst ◽

10.1002/chin.198620324 ◽

1986 ◽

Vol 17 (20) ◽

Author(s):

P. MAGNUS ◽

P. M. CAIRNS

Keyword(s):

Indole Alkaloid ◽

Alder Reaction ◽

Diels Alder ◽

Diels Alder Reaction ◽

Alkaloid Synthesis ◽

Enantiospecific Synthesis

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Synthesis oftrans-3,4-Dimethyl-4-(3-hydroxyphenyl)piperidine Opioid Antagonists: Application of theCis-Thermal Elimination of Carbonates to Alkaloid Synthesis

The Journal of Organic Chemistry ◽

10.1021/jo951403y ◽

1996 ◽

Vol 61 (2) ◽

pp. 587-597 ◽

Cited By ~ 17

Author(s):

John A. Werner ◽

Louis R. Cerbone ◽

Scott A. Frank ◽

Jeffrey A. Ward ◽

Parviz Labib ◽

...

Keyword(s):

Opioid Antagonists ◽

Alkaloid Synthesis ◽

Thermal Elimination

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Use of nitrogen and oxygen dipole ylides for alkaloid synthesis

ARKIVOC ◽

10.24820/ark.5550190.p010.416 ◽

2018 ◽

Vol 2018 (4) ◽

pp. 23-49 ◽

Cited By ~ 7

Author(s):

Albert Padwa

Keyword(s):

Alkaloid Synthesis

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ChemInform Abstract: Alkaloid Synthesis Using 2nd Generation Palladium-Catalyzed Cycloalkenylation. Diastereoselective Total Synthesis of α-Skytanthine (VII).

ChemInform ◽

10.1002/chin.201207153 ◽

2012 ◽

Vol 43 (7) ◽

pp. no-no

Author(s):

Kazutaka Takeda ◽

Masahiro Toyota

Keyword(s):

Total Synthesis ◽

2Nd Generation ◽

Alkaloid Synthesis ◽

Palladium Catalyzed

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ChemInform Abstract: NEW METHODS FOR ALKALOID SYNTHESIS. FACILE TOTAL SYNTHESES OF (.+-.)-O-METHYLJOUBERTIAMINE AND (.+-.)-MESEMBRINE

Chemischer Informationsdienst ◽

10.1002/chin.198004364 ◽

1980 ◽

Vol 11 (4) ◽

Author(s):

S. F. MARTIN ◽

T. A. PUCKETTE ◽

J. A. COLAPRET

Keyword(s):

Total Syntheses ◽

New Methods ◽

Alkaloid Synthesis

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ChemInform Abstract: Transition Metal Catalyzed Intramolecular (4 + 2) Cycloadditions: A Novel Method for the Assembly of Nitrogen Heterocycles and Its Application to Yohimban Alkaloid Synthesis.

ChemInform ◽

10.1002/chin.199627047 ◽

2010 ◽

Vol 27 (27) ◽

pp. no-no

Author(s):

P. A. WENDER ◽

T. E. SMITH

Keyword(s):

Transition Metal ◽

Nitrogen Heterocycles ◽

Alkaloid Synthesis ◽

Novel Method ◽

Transition Metal Catalyzed ◽

Metal Catalyzed

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ChemInform Abstract: Lewis Acid Catalyzed Ring-Opening Reactions of Semicyclic N,O-Acetals Possessing an Exocyclic Nitrogen Atom: Mechanistic Aspect and Application to Piperidine Alkaloid Synthesis.

ChemInform ◽

10.1002/chin.200221061 ◽

2010 ◽

Vol 33 (21) ◽

pp. no-no

Author(s):

Masaharu Sugiura ◽

Hiroyuki Hagio ◽

Ryoji Hirabayashi ◽

Shu Kobayashi

Keyword(s):

Nitrogen Atom ◽

Lewis Acid ◽

Ring Opening ◽

Alkaloid Synthesis ◽

Ring Opening Reactions ◽

Acid Catalyzed ◽

Mechanistic Aspect ◽

Exocyclic Nitrogen Atom

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ChemInform Abstract: Methods for Indole Alkaloid Synthesis. A Specific Procedure for Introducing the 6,7 Double Bond into Aspidosperma-Type Alkaloids via Thiolactam Dehydrogenation.

Chemischer Informationsdienst ◽

10.1002/chin.198620323 ◽

1986 ◽

Vol 17 (20) ◽

Author(s):

P. MAGNUS ◽

P. A. PAPPALARDO

Keyword(s):

Double Bond ◽

Indole Alkaloid ◽

Specific Procedure ◽

Alkaloid Synthesis

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ChemInform Abstract: GENERAL METHODS FOR ALKALOID SYNTHESIS. TOTAL SYNTHESIS OF RACEMIC LYCORAMINE

Chemischer Informationsdienst ◽

10.1002/chin.198237331 ◽

1982 ◽

Vol 13 (37) ◽

Author(s):

S. F. MARTIN ◽

P. J. GARRISON

Keyword(s):

Total Synthesis ◽

Alkaloid Synthesis

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