(Q59183523)

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Synthesis of chiral oligopeptides by means of catalytic asymmetric hydrogenation of dehydropeptides

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Synthesis of chiral oligopeptides by means of catalytic asymmetric hydrogenation of dehydropeptides (English)

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1 reference

Iwao Ojima

1

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T Noriko Yoda

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2

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Momoko Yatabe

series ordinal

3

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Toshiyuki Tanaka

series ordinal

4

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Tetsuo Kogure

series ordinal

5

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publication date

January 1984

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published in

Tetrahedron

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volume

40

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issue

8

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page(s)

1255-1268

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cites work

Asymmetric hydrogenation of alpha, beta-dehydroamino acid residue in cyclic dipeptides

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Mechanism and stereoselectivity of asymmetric hydrogenation

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Asymmetric hydrogenation of prochiral olefins catalyzed by rhodium complexes with chiral pyrrolidinodiphosphines. Crucial factors for the effective asymmetric induction

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Organofluorine synthesis via photofluorination: 3-fluoro-D-alanine and 2-deuterio analogue, antibacterials related to the bacterial cell wall

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Reactions of β-fluoroalanine and β-bromoalanine with D-amino acid oxidase

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Identification of two related pentapeptides from the brain with potent opiate agonist activity

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Structure-Activity Relationships of Enkephalin-Like Peptides

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Enkephalin analogues eliciting analgesia after intravenous injection

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Asymmetric synthesis. Production of optically active amino acids by catalytic hydrogenation

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Asymmetric catalytic reduction with transition metal complexes. I. Catalytic system of rhodium(I) with (-)-2,3-0-isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)butane, a new chiral diphosphine

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Asymmetric hydrogenation. Rhodium chiral bisphosphine catalyst

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Identifiers

DOI

10.1016/S0040-4020(01)82412-1

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release_fhxbn773jzd43lynhk753gnoxe

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(Q59183523)

Synthesis of chiral oligopeptides by means of catalytic asymmetric hydrogenation of dehydropeptides

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