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Literature DB >> 20174449

Synthetic Studies towards Maoecrystal V.

Feng Peng¹, Maolin Yu, Samuel J Danishefsky.

Abstract

The investigation of an intramolecular Diels-Alder reaction, en route to a projected total synthesis of maoecrystal V, is described.

Entities: CellLine Chemical Disease

Year: 2009 PMID： 20174449 PMCID： PMC2822274 DOI： 10.1016/j.tetlet.2009.09.050

Source DB: PubMed Journal: Tetrahedron Lett ISSN： 0040-4039 Impact factor: 2.415

6 in total

1. Syntheses of biologically active natural products and leading compounds for new pharmaceuticals employing effective construction of a polycyclic skeleton.

Authors: Masataka Ihara
Journal: Chem Pharm Bull (Tokyo) Date: 2006-06 Impact factor: 1.645

2. Pattern recognition in retrosynthetic analysis: snapshots in total synthesis.

Authors: Rebecca M Wilson; Samuel J Danishefsky
Journal: J Org Chem Date: 2007-06-08 Impact factor: 4.354

Review 3. The Diels--Alder reaction in total synthesis.

Authors: K C Nicolaou; Scott A Snyder; Tamsyn Montagnon; Georgios Vassilikogiannakis
Journal: Angew Chem Int Ed Engl Date: 2002-05-17 Impact factor: 15.336

4. Synthetic study toward the total synthesis of maoecrystal V.

Authors: Jianxian Gong; Guang Lin; Chuang-chuang Li; Zhen Yang
Journal: Org Lett Date: 2009-11-05 Impact factor: 6.005

5. Masked o-benzoquinones in organic synthesis.

Authors: Chun-Chen Liao; Rama Krishna Peddinti
Journal: Acc Chem Res Date: 2002-10 Impact factor: 22.384

6. Maoecrystal V, cytotoxic diterpenoid with a novel C19 skeleton from Isodon eriocalyx (Dunn.) hara.

Authors: Sheng-Hong Li; Jia Wang; Xue-Mei Niu; Yun-Heng Shen; Hong-Jie Zhang; Han-Dong Sun; Ma-Lin Li; Qin-E Tian; Yang Lu; Peng Cao; Qi-Tai Zheng
Journal: Org Lett Date: 2004-11-11 Impact factor: 6.005

6 in total

11 in total

1. Studies toward the synthesis of maoecrystal V.

Authors: Zhenhua Gu; Armen Zakarian
Journal: Org Lett Date: 2011-01-27 Impact factor: 6.005

2. Toward the total synthesis of maoecrystal V: an intramolecular Diels-Alder route to the maoecrystal V pentacyclic core with the appropriate relative stereochemistry.

Authors: Feng Peng; Samuel J Danishefsky
Journal: Tetrahedron Lett Date: 2011-04-27 Impact factor: 2.415

Synthetic Studies towards Maoecrystal V.

1. Syntheses of biologically active natural products and leading compounds for new pharmaceuticals employing effective construction of a polycyclic skeleton.

2. Pattern recognition in retrosynthetic analysis: snapshots in total synthesis.

Review 3. The Diels--Alder reaction in total synthesis.

4. Synthetic study toward the total synthesis of maoecrystal V.

5. Masked o-benzoquinones in organic synthesis.

6. Maoecrystal V, cytotoxic diterpenoid with a novel C19 skeleton from Isodon eriocalyx (Dunn.) hara.

1. Studies toward the synthesis of maoecrystal V.

2. Toward the total synthesis of maoecrystal V: an intramolecular Diels-Alder route to the maoecrystal V pentacyclic core with the appropriate relative stereochemistry.

3. A synthesis of the carbocyclic core of maoecrystal V.

4. Total synthesis of maoecrystal V: early-stage C-H functionalization and lactone assembly by radical cyclization.

5. Evaluation of 'east-to-west' ether-forming strategies for the total synthesis of maoecrystal V.

6. Oxidative Coupling of Enolates, Enol Silanes and Enamines: Methods and Natural Product Synthesis.

7. Total synthesis of (±)-maoecrystal V.

8. A synthesis of the carbon skeleton of maoecrystal V.

Review 9. Synthetic Strategies toward Natural Products Containing Contiguous Stereogenic Quaternary Carbon Atoms.

10. Enantioselective synthesis of (-)-maoecrystal V by enantiodetermining C-H functionalization.