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Literature DB >> 18175299

Enantioselective synthesis of (+)-monobromophakellin and (+)-phakellin: a concise phakellin annulation strategy applicable to Palau'amine.

Shaohui Wang¹, Daniel Romo.

Abstract

Mesh：

Substances：
Piperazines
phakellin

Year: 2008 PMID： 18175299 DOI： 10.1002/anie.200703998

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

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19 in total

1. Synthetic Studies on Palau'amine. Construction of the Cyclopentane Core via an Asymmetric 1,3-Dipolar Cycloaddition.

Authors: Kosuke Namba; Makto Inai; Uta Sundermeier; Thomas J Greshock; Robert M Williams
Journal: Tetrahedron Lett Date: 2010-12-15 Impact factor: 2.415

2. Synthetic access to the chlorocyclopentane cores of the proposed original and revised structures of palau'amine.

Authors: Michael S Bultman; Jun Ma; David Y Gin
Journal: Angew Chem Int Ed Engl Date: 2008 Impact factor: 15.336

3. Facile synthesis of the trans-fused azabicyclo[3.3.0]octane core of the palau'amines and the tricyclic core of the axinellamines from a common intermediate.

Authors: Manuel A Zancanella; Daniel Romo
Journal: Org Lett Date: 2008-08-12 Impact factor: 6.005

4. Generation and Reactivity of 2-Amido-1,3-diaminoallyl Cations: Cyclic Guanidine Annulations via Net (3 + 2) and (4 + 3) Cycloadditions.

Authors: V Raghavendra Rao Kovvuri; Haoran Xue; Daniel Romo
Journal: Org Lett Date: 2020-02-03 Impact factor: 6.005

5. Syntheses of Cyclic Guanidine-Containing Natural Products.

Authors: Yuyong Ma; Saptarshi De; Chuo Chen
Journal: Tetrahedron Date: 2015-02-25 Impact factor: 2.457

6. Facile Access to Ring-Fused Aminals via Direct α-Amination of Secondary Amines with ortho-Aminobenzaldehydes. Synthesis of Vasicine, Deoxyvasicine, Deoxyvasicinone, Mackinazolinone and Ruteacarpine.

Authors: Matthew T Richers; Indubhusan Deb; Alena Yu Platonova; Chen Zhang; Daniel Seidel
Journal: Synthesis (Stuttg) Date: 2013-10-06 Impact factor: 3.157

Enantioselective synthesis of (+)-monobromophakellin and (+)-phakellin: a concise phakellin annulation strategy applicable to Palau'amine.

1. Synthetic Studies on Palau'amine. Construction of the Cyclopentane Core via an Asymmetric 1,3-Dipolar Cycloaddition.

2. Synthetic access to the chlorocyclopentane cores of the proposed original and revised structures of palau'amine.

3. Facile synthesis of the trans-fused azabicyclo[3.3.0]octane core of the palau'amines and the tricyclic core of the axinellamines from a common intermediate.

4. Generation and Reactivity of 2-Amido-1,3-diaminoallyl Cations: Cyclic Guanidine Annulations via Net (3 + 2) and (4 + 3) Cycloadditions.

5. Syntheses of Cyclic Guanidine-Containing Natural Products.

6. Facile Access to Ring-Fused Aminals via Direct α-Amination of Secondary Amines with ortho-Aminobenzaldehydes. Synthesis of Vasicine, Deoxyvasicine, Deoxyvasicinone, Mackinazolinone and Ruteacarpine.

7. Enantioselective total syntheses of (-)-palau'amine, (-)-axinellamines, and (-)-massadines.

8. Exploring symmetry-based logic for a synthesis of palau'amine.

9. Total syntheses of (+/-)-massadine and massadine chloride.

Review 10. A submarine journey: the pyrrole-imidazole alkaloids.