Efficient synthesis of protected cyclopropyl beta-aspartylphosphates.

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Stereoselective synthesis of β-hydroxy enamines, aminocyclopropanes, and 1,3-amino alcohols via asymmetric catalysis.Focus on phosphoaspartate and phosphoglutamate.Helical screw-sense preferences of peptides based on chiral, Cα-tetrasubstituted α-amino acids.

P2860

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P2860

Efficient synthesis of protected cyclopropyl beta-aspartylphosphates.

Item

http://www.wikidata.org/entity/Q44760680

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2004 nî lūn-bûn

@nan

2004年の論文

@ja

2004年学术文章

@wuu

2004年学术文章

@zh

2004年学术文章

@zh-cn

2004年学术文章

@zh-hans

2004年学术文章

@zh-my

2004年学术文章

@zh-sg

2004年學術文章

@yue

2004年學術文章

@zh-hant

name

Efficient synthesis of protected cyclopropyl beta-aspartylphosphates.

@en

Efficient synthesis of protected cyclopropyl beta-aspartylphosphates.

@nl

type

Item

label

Efficient synthesis of protected cyclopropyl beta-aspartylphosphates.

@en

Efficient synthesis of protected cyclopropyl beta-aspartylphosphates.

@nl

prefLabel

Efficient synthesis of protected cyclopropyl beta-aspartylphosphates.

@en

Efficient synthesis of protected cyclopropyl beta-aspartylphosphates.

@nl

P1476

Efficient synthesis of protected cyclopropyl beta-aspartylphosphates.

@en

P2093

Jonathan P H Charmant

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

Luke A Adams

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

Magnus Walter

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

Russell J Cox

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

William G Whittingham

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

P2860

Aspartyl phosphonates and phosphoramidates: the first synthetic inhibitors of bacterial aspartate-semialdehyde dehydrogenase.

Difluoromethylene analogues of aspartyl phosphate: the first synthetic inhibitors of aspartate semi-aldehyde dehydrogenase.

A novel one-pot method for the preparation of pyrazoles by 1,3-dipolar cycloadditions of diazo compounds generated in situ.

Diastereoselective synthesis of cyclopropane amino acids using diazo compounds generated in situ.

Synthesis of the 2-amino-4-phosphonobutanoic acid analogues (E)- and (Z)-2-amino-2,3-methano-4-phosphonobutanoic acid and their evaluation as inhibitors of hippocampal excitatory neurotransmission.

P304

542-553

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P31

scholarly article

P356

10.1039/B311322A

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

P433

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

P478

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

P577

2004-01-21T00:00:00Z

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

P5875

8880359

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P698

14770233

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

Efficient synthesis of protected cyclopropyl beta-aspartylphosphates.

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P2860

P2860

Efficient synthesis of protected cyclopropyl beta-aspartylphosphates.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698