Use of aza-Cope rearrangement-Mannich cyclization reactions to achieve a general entry to Melodinus and Aspidosperma alkaloids. Stereocontrolled total syntheses of (.+-.)-deoxoapodine, (.+-.)-meloscine, and (.+-.)-epimeloscine and a formal synthesis of (.+-.)-1-acetylaspidoalbidine

ChemInform Abstract: Use of Aza-Cope Rearrangement-Mannich Cyclization Reactions to Achieve a General Entry to Melodinus and Aspidosperma Alkaloids. Stereocontrolled Total Syntheses of (.+-.)-Deoxoapodine, (.+-.)- Meloscine, and (.+-.)-Epimeloscine and a

ChemInform ◽

10.1002/chin.199130270 ◽

2010 ◽

Vol 22 (30) ◽

pp. no-no

Author(s):

L. E. OVERMAN ◽

G. M. ROBERTSON ◽

A. J. ROBICHAUD

Keyword(s):

Cope Rearrangement ◽

Cyclization Reactions ◽

Total Syntheses ◽

ChemInform Abstract: Synthesis Applications of Cationic Aza-Cope Rearrangements. Part 18. Scope and Mechanism of Tandem Cationic Aza-Cope Rearrangement-Mannich Cyclization Reactions.

ChemInform ◽

10.1002/chin.198842202 ◽

1988 ◽

Vol 19 (42) ◽

Author(s):

E. J. JACOBSEN ◽

J. LEVIN ◽

L. E. OVERMAN

Keyword(s):

Cope Rearrangement ◽

Cyclization Reactions ◽

Mannich Cyclization ◽

Cope Rearrangements

Synthesis applications of cationic aza-Cope rearrangements. Part 18. Scope and mechanism of tandem cationic aza-Cope rearrangement-Mannich cyclization reactions

Journal of the American Chemical Society ◽

10.1021/ja00221a037 ◽

1988 ◽

Vol 110 (13) ◽

pp. 4329-4336 ◽

Cited By ~ 51

Author(s):

E. Jon. Jacobsen ◽

Jeremy. Levin ◽

Larry E. Overman

Keyword(s):

Cope Rearrangement ◽

Cyclization Reactions ◽

Mannich Cyclization ◽

Cope Rearrangements

The Rearrangement of 2,3-Epoxysulfonates and Its Application to Natural Products Syntheses: Formal Synthesis of (-)-Aphanorphine and Total Syntheses of (-)-α-Herbertenol and (-)-Herbertenediol.

ChemInform ◽

10.1002/chin.200347028 ◽

2003 ◽

Vol 34 (47) ◽

Author(s):

Yasuyuki Kita ◽

Junko Futamura ◽

Yusuke Ohba ◽

Yoshinari Sawama ◽

Jnaneshwara K. Ganesh ◽

...

Keyword(s):

Natural Products ◽

Formal Synthesis ◽

Tandem Cationicaza-Cope Rearrangement−Mannich Cyclization Approach to the Core Structure of FR901483 via a Bridgehead Iminium Ion

Organic Letters ◽

10.1021/ol010029n ◽

2001 ◽

Vol 3 (9) ◽

pp. 1347-1349 ◽

Cited By ~ 47

Author(s):

Kay M. Brummond ◽

Jianliang Lu

Keyword(s):

Core Structure ◽

Cope Rearrangement ◽

The Core ◽

Iminium Ion ◽

ChemInform Abstract: Quinine-Catalyzed Asymmetric Domino Mannich-Cyclization Reactions of 3-Isothiocyanato Oxindoles with Imines for the Synthesis of Spirocyclic Oxindoles.

ChemInform ◽

10.1002/chin.201524112 ◽

2015 ◽

Vol 46 (24) ◽

pp. no-no

Author(s):

Mei Bai ◽

Bao-Dong Cui ◽

Jian Zuo ◽

Jian-Qiang Zhao ◽

Yong You ◽

...

Keyword(s):

Cyclization Reactions ◽

Connecting C19 Norditerpenoids to C20 Diterpenes: Total Syntheses of 6-Hydroxy-5,6-dehydrosugiol, 6-Hydroxysugiol, and Taiwaniaquinone H, and Formal Synthesis of Dichroanone

Synthesis ◽

10.1055/s-0029-1218806 ◽

2010 ◽

Cited By ~ 1

Author(s):

Karl Gademann ◽

Chandan Jana ◽

Rosario Scopelliti

Keyword(s):

Formal Synthesis ◽

Total Syntheses of Hyperforin and Papuaforins A-C, and Formal Synthesis of Nemorosone through a Gold(I)-Catalyzed Carbocyclization

Angewandte Chemie International Edition ◽

10.1002/anie.201403939 ◽

2014 ◽

Vol 53 (26) ◽

pp. 6701-6704 ◽

Cited By ~ 46

Author(s):

Gabriel Bellavance ◽

Louis Barriault

Keyword(s):

Formal Synthesis ◽

Total Syntheses of Vellosimine,N-Methylvellosimine, and 10-Methoxyvellosimine and Formal Synthesis of 16-Epinormacusine B through a [5+2] Cycloaddition

European Journal of Organic Chemistry ◽

10.1002/ejoc.201600870 ◽

2016 ◽

Vol 2016 (28) ◽

pp. 4893-4899 ◽

Cited By ~ 11

Author(s):

Sebastian Krüger ◽

Tanja Gaich

Keyword(s):

Formal Synthesis ◽

Controlling Diastereoselectivity in the Tandem Microwave-Assisted Aza-Cope Rearrangement—Mannich Cyclization.

ChemInform ◽

10.1002/chin.200732115 ◽

2007 ◽

Vol 38 (32) ◽

Author(s):

Benjamin F. Johnson ◽

Edwin L. Marrero ◽

Wesley A. Turley ◽

Harriet A. Lindsay

Keyword(s):

Cope Rearrangement ◽

Microwave Assisted ◽