Literature DB >> 16047049

Natural guanidine derivatives.

Roberto G S Berlinck1, Miriam H Kossuga.   

Abstract

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Year:  2005        PMID： 16047049     DOI： 10.1039/b209227c

Source DB:  PubMed          Journal:  Nat Prod Rep        ISSN： 0265-0568            Impact factor:   13.423


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  23 in total

1.  Asymmetric total synthesis of (+)-merobatzelladine B.

Authors:  Nicholas R Babij; John P Wolfe
Journal:  Angew Chem Int Ed Engl       Date:  2012-03-16       Impact factor: 15.336

2.  Syntheses of Cyclic Guanidine-Containing Natural Products.

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

3.  Concise synthesis of guanidine-containing heterocycles using the Biginelli reaction.

Authors:  Bradley L Nilsson; Larry E Overman
Journal:  J Org Chem       Date:  2006-09-29       Impact factor: 4.354

4.  Desymmetrization of meso-2,5-diallylpyrrolidinyl ureas through asymmetric palladium-catalyzed carboamination: stereocontrolled synthesis of bicyclic ureas.

Authors:  Nicholas R Babij; John P Wolfe
Journal:  Angew Chem Int Ed Engl       Date:  2013-07-03       Impact factor: 15.336

5.  A convergent approach to batzelladine alkaloids. Total syntheses of (+)-batzelladine E, (-)-dehydrobatzelladine C, and (+)-batzelladine K.

Authors:  Christos Economou; Justin P Romaire; Tony Z Scott; Brendan T Parr; Seth B Herzon
Journal:  Tetrahedron       Date:  2018-04-18       Impact factor: 2.457

Review 6.  Recent progress in neuroactive marine natural products.

Authors:  Ryuichi Sakai; Geoffrey T Swanson
Journal:  Nat Prod Rep       Date:  2014-01-17       Impact factor: 13.423

7.  Synthesis of 7-epineoptilocaulin, mirabilin B, and isoptilocaulin. A unified biosynthetic proposal for the ptilocaulin and batzelladine alkaloids. Synthesis and structure revision of netamines E and G.

Authors:  Min Yu; Susan S Pochapsky; Barry B Snider
Journal:  J Org Chem       Date:  2008-10-18       Impact factor: 4.354

8.  A stereodivergent strategy to both product enantiomers from the same enantiomer of a stereoinducing catalyst: agelastatin A.

Authors:  Barry M Trost; Guangbin Dong
Journal:  Chemistry       Date:  2009-07-13       Impact factor: 5.236

9.  Evolution of a strategy for the synthesis of structurally complex batzelladine alkaloids. Enantioselective total synthesis of the proposed structure of batzelladine F and structural revision.

Authors:  Frederick Cohen; Larry E Overman
Journal:  J Am Chem Soc       Date:  2006-03-01       Impact factor: 15.419

10.  Enantioselective total synthesis of batzelladine F and definition of its structure.

Authors:  Frederick Cohen; Larry E Overman
Journal:  J Am Chem Soc       Date:  2006-03-01       Impact factor: 15.419
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