Linear dialdehydes as promising substrates for aminocatalyzed transformations.

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Linear dialdehydes as promising substrates for aminocatalyzed transformations.

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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2015年论文

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2015年论文

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Linear dialdehydes as promising substrates for aminocatalyzed transformations.

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Linear dialdehydes as promising substrates for aminocatalyzed transformations.

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Linear dialdehydes as promising substrates for aminocatalyzed transformations.

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P1476

Linear dialdehydes as promising substrates for aminocatalyzed transformations.

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P2093

Anoop Singh

http://www.w3.org/2001/XMLSchema#string

Indresh Kumar

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Nisar A Mir

http://www.w3.org/2001/XMLSchema#string

Panduga Ramaraju

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P2860

Asymmetric Organocatalytic Domino Reactions

In the Golden Age of Organocatalysis

Proline-Catalyzed Direct Asymmetric Aldol Reactions

Novel syntheses of hexahydro-1H-pyrrolo[1,2-a]ĭmidazoles and Octahydroimidazo[1,2-a]pyridines.

Application of the chloro ketal Claisen reaction to the total synthesis of squalene

Stereocontrolled organocatalytic synthesis of prostaglandin PGF2α in seven steps.

Enamine-based organocatalysis with proline and diamines: the development of direct catalytic asymmetric Aldol, Mannich, Michael, and Diels-alder reactions.

Asymmetric organocatalysis.

Enantioselective organocatalytic singly occupied molecular orbital activation: the enantioselective alpha-enolation of aldehydes.

meso Compounds: stepchildren or favored children of stereoselective synthesis?

P304

1280-1293

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P31

scholarly article

P356

10.1039/C4OB01805B

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2015-02-01T00:00:00Z

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P698

25492696

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