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Literature DB >> 16771455

Synthetic approaches to enantiomerically pure 8-azabicyclo[3.2.1]octane derivatives.

Gian P Pollini¹, Simonetta Benetti, Carmela De Risi, Vinicio Zanirato.

Abstract

Entities: Chemical

Mesh：

Substances：

Year: 2006 PMID： 16771455 DOI： 10.1021/cr050995+

Source DB: PubMed Journal: Chem Rev ISSN： 0009-2665 Impact factor: 60.622

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14 in total

1. Intramolecular alkene carboamination reactions for the synthesis of enantiomerically enriched tropane derivatives.

Authors: Danielle M Schultz; John P Wolfe
Journal: Org Lett Date: 2011-05-11 Impact factor: 6.005

2. The last step in cocaine biosynthesis is catalyzed by a BAHD acyltransferase.

Authors: Gregor Wolfgang Schmidt; Jan Jirschitzka; Tiffany Porta; Michael Reichelt; Katrin Luck; José Carlos Pardo Torre; Franziska Dolke; Emmanuel Varesio; Gérard Hopfgartner; Jonathan Gershenzon; John Charles D'Auria
Journal: Plant Physiol Date: 2014-11-18 Impact factor: 8.340

3. Organometallic enantiomeric scaffolding: general access to 2-substituted oxa- and azabicyclo[3.2.1]octenes via a Brønsted acid catalyzed [5 + 2] cycloaddition reaction.

Authors: Ethel C Garnier; Lanny S Liebeskind
Journal: J Am Chem Soc Date: 2008-05-15 Impact factor: 15.419

4. Metal-free [3 + 2 + 1]/[2 + 2 + 1] biscyclization: stereospecific construction with concomitant functionalization of indolizin-5(1H)-one.

Authors: Tuan-Jie Li; Zhong-Qiu Liu; Hong-Mei Yin; Chang-Sheng Yao; Bo Jiang; Xiang-Shan Wang; Shu-Jiang Tu; Xiu-Ling Li; Guigen Li
Journal: J Org Chem Date: 2013-11-07 Impact factor: 4.354

5. Enantioselective total synthesis of (-)-colchicine, (+)-demecolcinone and metacolchicine: determination of the absolute configurations of the latter two alkaloids.

Authors: Bo Chen; Xin Liu; Ya-Jian Hu; Dong-Mei Zhang; Lijuan Deng; Jieyu Lu; Long Min; Wen-Cai Ye; Chuang-Chuang Li
Journal: Chem Sci Date: 2017-05-05 Impact factor: 9.825

10. Crystal structure of (1R,5S)-endo-(8-methyl-8-azoniabi-cyclo-[3.2.1]oct-3-yl)ammonium aqua-tri-chlorido-nitratocopper(II).

Authors: Sergey N Britvin; Andrey M Rumyantsev
Journal: Acta Crystallogr E Crystallogr Commun Date: 2017-10-20

Synthetic approaches to enantiomerically pure 8-azabicyclo[3.2.1]octane derivatives.

1. Intramolecular alkene carboamination reactions for the synthesis of enantiomerically enriched tropane derivatives.

2. The last step in cocaine biosynthesis is catalyzed by a BAHD acyltransferase.

3. Organometallic enantiomeric scaffolding: general access to 2-substituted oxa- and azabicyclo[3.2.1]octenes via a Brønsted acid catalyzed [5 + 2] cycloaddition reaction.

4. Metal-free [3 + 2 + 1]/[2 + 2 + 1] biscyclization: stereospecific construction with concomitant functionalization of indolizin-5(1H)-one.

5. Enantioselective total synthesis of (-)-colchicine, (+)-demecolcinone and metacolchicine: determination of the absolute configurations of the latter two alkaloids.

6. The 7-aza-norbornane nucleus of epibatidine: 7-aza-bicyclo-[2.2.1]heptan-7-ium chloride.

7. Rh(iii)-catalyzed regioselective intermolecular N-methylene Csp³-H bond carbenoid insertion.

8. Determination of the relative configuration of tropinone and granatanone aldols by using TBDMS ethers.

9. Catalytic enantioselective 1,3-dipolar cycloadditions of azomethine ylides for biology-oriented synthesis.

10. Crystal structure of (1R,5S)-endo-(8-methyl-8-azoniabi-cyclo-[3.2.1]oct-3-yl)ammonium aqua-tri-chlorido-nitratocopper(II).