An approach towards azafuranomycin analogs by gold-catalyzed cycloisomerization of allenes: synthesis of (αS,2R)-(2,5-dihydro-1H-pyrrol-2-yl)glycine.

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An approach towards azafuranomycin analogs by gold-catalyzed cycloisomerization of allenes: synthesis of (αS,2R)-(2,5-dihydro-1H-pyrrol-2-yl)glycine.

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2013 nî lūn-bûn

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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An approach towards azafuranom ...... ihydro-1H-pyrrol-2-yl)glycine.

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An approach towards azafuranom ...... ihydro-1H-pyrrol-2-yl)glycine.

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An approach towards azafuranom ...... ihydro-1H-pyrrol-2-yl)glycine.

@en

An approach towards azafuranom ...... ihydro-1H-pyrrol-2-yl)glycine.

@nl

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An approach towards azafuranom ...... ihydro-1H-pyrrol-2-yl)glycine.

@en

An approach towards azafuranom ...... ihydro-1H-pyrrol-2-yl)glycine.

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P1476

An approach towards azafuranom ...... ihydro-1H-pyrrol-2-yl)glycine.

@en

P2093

Jörg Erdsack

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Norbert Krause

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P2860

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Cyclobutane amino acid analogues of furanomycin obtained by a formal [2 + 2] cycloaddition strategy promoted by methylaluminoxane.

Amino-acids and peptides. VII. The synthesis of the fourteen-membered cyclodepsipeptides D-D-, L-L, and D-L-cyclodi-(beta-seryloxypropionyl).

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Convergent approach to pumiliotoxin alkaloids. Asymmetric total synthesis of (+)-pumiliotoxins A, B, and 225F.

Straightforward syntheses of furanomycin derivatives and their biological evaluation.

First asymmetric synthesis of 6-hydroxy-4-sphingenine-containing ceramides. Use of chiral propargylic alcohols to prepare a lipid found in human skin.

o-Iodoxybenzoic acid (IBX) as a viable reagent in the manipulation of nitrogen- and sulfur-containing substrates: scope, generality, and mechanism of IBX-mediated amine oxidations and dithiane deprotections.

P304

1936-1942

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scholarly article

P356

10.3762/BJOC.9.229

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P478

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P577

2013-09-25T00:00:00Z

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258350502

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24204404

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P932

3817573

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