Inside Cover: Iodine-Catalyzed Highly Diastereoselective Synthesis oftrans-2,6-Disubstituted-3,4-Dihydropyrans: Application to Concise Construction of C28-C37 Bicyclic Core of (+)-Sorangicin A (Chem. Eur. J. 7/2010)

Debendra K. Mohapatra; Pragna P. Das; Manas Ranjan Pattanayak; J. S. Yadav

doi:10.1002/chem.201090023

Inside Cover: Iodine-Catalyzed Highly Diastereoselective Synthesis oftrans-2,6-Disubstituted-3,4-Dihydropyrans: Application to Concise Construction of C28-C37 Bicyclic Core of (+)-Sorangicin A (Chem. Eur. J. 7/2010)

Chemistry - A European Journal ◽

10.1002/chem.201090023 ◽

2010 ◽

Vol 16 (7) ◽

pp. 2008-2008

Author(s):

Debendra K. Mohapatra ◽

Pragna P. Das ◽

Manas Ranjan Pattanayak ◽

J. S. Yadav

Keyword(s):

Diastereoselective Synthesis ◽

Sorangicin A

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ChemInform Abstract: Iodine-Catalyzed Highly Diastereoselective Synthesis of trans-2,6-Disubstituted-3,4-dihydropyrans: Application to Concise Construction of C28-C37 Bicyclic Core of (+)-Sorangicin A.

ChemInform ◽

10.1002/chin.201024121 ◽

2010 ◽

Vol 41 (24) ◽

pp. no-no

Author(s):

Debendra K. Mohapatra ◽

Pragna P. Das ◽

Manas Ranjan Pattanayak ◽

J. S. Yadav

Keyword(s):

Diastereoselective Synthesis ◽

Sorangicin A

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Inside Cover: Iodine-Catalyzed Highly Diastereoselective Synthesis of trans-2,6-Disubstituted-3,4-Dihydropyrans: Application to Concise Construction of C28-C37 Bicyclic Core of (+)-Sorangicin A (Chem. Eur. J. 7/2010)

Chemistry - A European Journal ◽

10.1002/chem.201090036 ◽

2010 ◽

Vol 16 (9) ◽

pp. 2648-2648

Author(s):

Debendra K. Mohapatra ◽

Pragna P. Das ◽

Manas Ranjan Pattanayak ◽

J. S. Yadav

Keyword(s):

Diastereoselective Synthesis ◽

Sorangicin A

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Iodine-Catalyzed Highly Diastereoselective Synthesis oftrans-2,6-Disubstituted-3,4-Dihydropyrans: Application to Concise Construction of C28-C37 Bicyclic Core of (+)-Sorangicin A

Chemistry - A European Journal ◽

10.1002/chem.200902999 ◽

2010 ◽

Vol 16 (7) ◽

pp. 2072-2078 ◽

Cited By ~ 41

Author(s):

Debendra K. Mohapatra ◽

Pragna P. Das ◽

Manas Ranjan Pattanayak ◽

J. S. Yadav

Keyword(s):

Diastereoselective Synthesis ◽

Sorangicin A

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Diastereoselective synthesis of β-amino alcohols with two or three chiral centers.

Tetrahedron Letters ◽

10.1016/s0040-4039(01)94542-3 ◽

1979 ◽

Vol 19 (15) ◽

pp. 1355-1356

Author(s):

R Haro-Ramos

Keyword(s):

Amino Alcohols ◽

Diastereoselective Synthesis ◽

Chiral Centers

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1604096: CeO2 nanoparticles: a robust and reusable heterogeneous catalyst for the diastereoselective synthesis of β-acetamido esters – ESI

Journal of Chemical Research ◽

10.3184/174751916x14683300159522 ◽

2016 ◽

Keyword(s):

Heterogeneous Catalyst ◽

Ceo2 Nanoparticles ◽

Diastereoselective Synthesis

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Faculty Opinions recommendation of The antibiotic sorangicin A inhibits promoter DNA unwinding in a Mycobacterium tuberculosis rifampicin-resistant RNA polymerase.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.739060487.793580432 ◽

2020 ◽

Author(s):

Neeraj Dhar

Keyword(s):

Mycobacterium Tuberculosis ◽

Rna Polymerase ◽

Dna Unwinding ◽

Sorangicin A ◽

Promoter Dna

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Naturally Occurring Organic Acid-catalyzed Facile Diastereoselective Synthesis of Biologically Active (E)-3-(arylimino)indolin-2-one Derivatives in Water at Room Temperature

Current Organic Chemistry ◽

10.2174/1385272822666190924182538 ◽

2019 ◽

Vol 23 (16) ◽

pp. 1778-1788 ◽

Cited By ~ 5

Author(s):

Gurpreet Kaur ◽

Arvind Singh ◽

Kiran Bala ◽

Mamta Devi ◽

Anjana Kumari ◽

...

Keyword(s):

Room Temperature ◽

Biologically Active ◽

Environmentally Benign ◽

Diastereoselective Synthesis ◽

Substituted Anilines ◽

Reaction Conditions ◽

Naturally Occurring ◽

Acid Catalyzed ◽

Reaction Media ◽

Column Chromatographic

A simple, straightforward and efficient method has been developed for the synthesis of (E)-3-(arylimino)indolin-2-one derivatives and (E)-2-((4-methoxyphenyl)imino)- acenaphthylen-1(2H)-one. The synthesis of these biologically-significant scaffolds was achieved from the reactions of various substituted anilines and isatins or acenaphthaquinone, respectively, using commercially available, environmentally benign and naturally occurring organic acids such as mandelic acid or itaconic acid as catalyst in aqueous medium at room temperature. Mild reaction conditions, energy efficiency, good to excellent yields, environmentally benign conditions, easy isolation of products, no need of column chromatographic separation and the reusability of reaction media are some of the significant features of the present protocol.

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