Addressing the Nature of Phosphinidene Sulfides via the Synthesis of P-S Heterocycles.

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Addressing the Nature of Phosphinidene Sulfides via the Synthesis of P-S Heterocycles.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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Addressing the Nature of Phosphinidene Sulfides via the Synthesis of P-S Heterocycles.

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Addressing the Nature of Phosphinidene Sulfides via the Synthesis of P-S Heterocycles.

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Addressing the Nature of Phosphinidene Sulfides via the Synthesis of P-S Heterocycles.

@en

Addressing the Nature of Phosphinidene Sulfides via the Synthesis of P-S Heterocycles.

@nl

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Addressing the Nature of Phosphinidene Sulfides via the Synthesis of P-S Heterocycles.

@en

Addressing the Nature of Phosphinidene Sulfides via the Synthesis of P-S Heterocycles.

@nl

P1476

Addressing the Nature of Phosphinidene Sulfides via the Synthesis of P-S Heterocycles

@en

P2093

Cameron M E Graham

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Charles L B Macdonald

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James A Wisner

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Paul D Boyle

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P2860

The modern interpretation of the Wittig reaction mechanism.

SHELXT - integrated space-group and crystal-structure determination.

Reactivity and selectivity in the Wittig reaction: a computational study.

Mechanism and Scope of Phosphinidene Transfer from Dibenzo-7-phosphanorbornadiene Compounds.

Ring opening of a sterically crowded 1,2-oxaphosphetane complex.

Isomerization of Secondary Phosphirane into Terminal Phosphinidene Complexes: An Analogy between Monovalent Phosphorus and Transition Metals.

A novel route to C-unsubstituted 1,2-oxaphosphetane and 1,2-oxaphospholane complexes.

Über Triphenyl-phosphin-methylene als olefinbildende Reagenzien (I. Mitteil

The Wittig olefination reaction and modifications involving phosphoryl-stabilized carbanions. Stereochemistry, mechanism, and selected synthetic aspects

Zur Reaktionsweise des Pentaphenyl-phosphors und einiger Derivate

P304

743-749

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P31

scholarly article

P356

10.1002/CHEM.201705198

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P407

English

P433

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P478

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P50

Paul J Ragogna

P577

2017-12-07T00:00:00Z

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P698

29106762

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