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Literature DB >> 17311127

Formal synthesis of (+)-SCH 351448: the Prins cyclization approach.

Kok-Ping Chan¹, Yvonne Hui Ling, Teck-Peng Loh.

Abstract

The formal synthesis of (+)-SCH 351448 has been accomplished with the catalytic Prins cyclization strategy, yielding the monomeric unit as a single isomer.

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Year: 2007 PMID： 17311127 DOI： 10.1039/b616558c

Source DB: PubMed Journal: Chem Commun (Camb) ISSN： 1359-7345 Impact factor: 6.222

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Cited

8 in total

1. Total synthesis of (+)-SCH 351448.

Authors: Kaicheng Zhu; James S Panek
Journal: Org Lett Date: 2011-08-11 Impact factor: 6.005

2. Assignment of absolute configuration to SCH 351448 via total synthesis.

Authors: Lael L Cheung; Shinji Marumoto; Christopher D Anderson; Scott D Rychnovsky
Journal: Org Lett Date: 2008-06-11 Impact factor: 6.005

3. Synthesis of (-)-okilactomycin by a Prins-type fragment-assembly strategy.

Authors: Jason M Tenenbaum; William J Morris; Daniel W Custar; Karl A Scheidt
Journal: Angew Chem Int Ed Engl Date: 2011-05-10 Impact factor: 15.336

4. Achmatowicz Reaction and its Application in the Syntheses of Bioactive Molecules.

Authors: Arun K Ghosh; Margherita Brindisi
Journal: RSC Adv Date: 2016-11-24 Impact factor: 3.361

5. Total synthesis of (+)-roxaticin via C-C bond forming transfer hydrogenation: a departure from stoichiometric chiral reagents, auxiliaries, and premetalated nucleophiles in polyketide construction.

Authors: Soo Bong Han; Abbas Hassan; In Su Kim; Michael J Krische
Journal: J Am Chem Soc Date: 2010-11-10 Impact factor: 15.419

Formal synthesis of (+)-SCH 351448: the Prins cyclization approach.

1. Total synthesis of (+)-SCH 351448.

2. Assignment of absolute configuration to SCH 351448 via total synthesis.

3. Synthesis of (-)-okilactomycin by a Prins-type fragment-assembly strategy.

4. Achmatowicz Reaction and its Application in the Syntheses of Bioactive Molecules.

5. Total synthesis of (+)-roxaticin via C-C bond forming transfer hydrogenation: a departure from stoichiometric chiral reagents, auxiliaries, and premetalated nucleophiles in polyketide construction.

6. One Carbon Homologation of Halides to Benzyl Ethers.

7. Rhenium(VII) catalysis of Prins cyclization reactions.

8. Formal synthesis of (-)-kendomycin featuring a Prins-cyclization to construct the macrocycle.