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Literature DB >> 15798978

Total synthesis of (-)-laulimalide: Pd-catalyzed stereospecific ring construction of the substituted 3,6-dihydro[2H]pyran units.

Jun'ichi Uenishi¹, Masashi Ohmi.

Abstract

Entities: Chemical

Mesh：

Substances：

Year: 2005 PMID： 15798978 DOI： 10.1002/anie.200500029

Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN： 1433-7851 Impact factor: 15.336

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8 in total

1. Total synthesis of laulimalide: synthesis of the northern and southern fragments.

Authors: Barry M Trost; W Michael Seganish; Cheol K Chung; Dominique Amans
Journal: Chemistry Date: 2012-02-03 Impact factor: 5.236

Review 2. Marine Mollusk-Derived Agents with Antiproliferative Activity as Promising Anticancer Agents to Overcome Chemotherapy Resistance.

Authors: Maria Letizia Ciavatta; Florence Lefranc; Marianna Carbone; Ernesto Mollo; Margherita Gavagnin; Tania Betancourt; Ramesh Dasari; Alexander Kornienko; Robert Kiss
Journal: Med Res Rev Date: 2016-12-07 Impact factor: 12.944

3. Re₂ O₇ -Mediated Dehydrative Cyclization Reactions: Total Synthesis of Herboxidiene and Its 12-Desmethyl Analogue.

Authors: Tyler M Rohrs; Qi Qin; Paul E Floreancig
Journal: Angew Chem Int Ed Engl Date: 2017-07-28 Impact factor: 15.336

4. The regio- and stereospecific intermolecular dehydrative alkoxylation of allylic alcohols catalyzed by a gold(I) N-heterocyclic carbene complex.

Authors: Paramita Mukherjee; Ross A Widenhoefer
Journal: Chemistry Date: 2013-01-24 Impact factor: 5.236

Total synthesis of (-)-laulimalide: Pd-catalyzed stereospecific ring construction of the substituted 3,6-dihydro[2H]pyran units.

1. Total synthesis of laulimalide: synthesis of the northern and southern fragments.

Review 2. Marine Mollusk-Derived Agents with Antiproliferative Activity as Promising Anticancer Agents to Overcome Chemotherapy Resistance.

3. Re₂ O₇ -Mediated Dehydrative Cyclization Reactions: Total Synthesis of Herboxidiene and Its 12-Desmethyl Analogue.

4. The regio- and stereospecific intermolecular dehydrative alkoxylation of allylic alcohols catalyzed by a gold(I) N-heterocyclic carbene complex.

5. Evaluating transition-metal-catalyzed transformations for the synthesis of laulimalide.

6. Fragmentation of bicyclic γ-silyloxy-β-hydroxy-α-diazolactones as an approach to ynolides.

7. Palladium-catalysed cyclisation of alkenols: Synthesis of oxaheterocycles as core intermediates of natural compounds.

Review 8. Mitotic Poisons in Research and Medicine.

Total synthesis of (-)-laulimalide: Pd-catalyzed stereospecific ring construction of the substituted 3,6-dihydro[2H]pyran units.

1. Total synthesis of laulimalide: synthesis of the northern and southern fragments.

Review 2. Marine Mollusk-Derived Agents with Antiproliferative Activity as Promising Anticancer Agents to Overcome Chemotherapy Resistance.

3. Re2 O7 -Mediated Dehydrative Cyclization Reactions: Total Synthesis of Herboxidiene and Its 12-Desmethyl Analogue.

4. The regio- and stereospecific intermolecular dehydrative alkoxylation of allylic alcohols catalyzed by a gold(I) N-heterocyclic carbene complex.

5. Evaluating transition-metal-catalyzed transformations for the synthesis of laulimalide.

6. Fragmentation of bicyclic γ-silyloxy-β-hydroxy-α-diazolactones as an approach to ynolides.

7. Palladium-catalysed cyclisation of alkenols: Synthesis of oxaheterocycles as core intermediates of natural compounds.

Review 8. Mitotic Poisons in Research and Medicine.

3. Re₂ O₇ -Mediated Dehydrative Cyclization Reactions: Total Synthesis of Herboxidiene and Its 12-Desmethyl Analogue.