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The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.

The Palladium‐Catalyzed Cross‐Coupling Reactions of Organotin Reagents with Organic Electrophiles [New Synthetic Methods (58)]

Stille, John K.·1986·Angewandte Chemie International Edition in English

Abstract

The cross‐coupling of organotin reagents with a variety of organic electrophiles, catalyzed by palladium, provides a novel method for generating a carbon‐carbon bond. Because this mild, versatile reaction is tolerant of a wide variety of functional groups on either coupling partner, is stereospecific and regioselective, and gives high yields of product, it is ideal for use in the synthesis of elaborate organic molecules. When the coupling reaction is carried out in the presence of carbon monoxide, instead of a direct coupling, carbon monoxide insertion takes place, stitching the two coupling partners together and generating a ketone.

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Metadata

Authors
Stille, J. K.
Venue
Angewandte Chemie International Edition in English
Publisher
Wiley
Published
1986-06
Volume
25
Issue
6
Pages
508-524
ISSN
0570-0833 (ISSN-L)
OpenAlex
W2024122111
Cited by
3,394
References
3
FWCI
17.92
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: The Palladium‐Catalyzed Cross‐Coupling Reactions of Organotin Reagents with Organic Electrophiles [New Synthetic Methods (58)]. https://app.cochat.ai/papers/10.1002/anie.198605081
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Stille, J. K. (1986). The Palladium‐Catalyzed Cross‐Coupling Reactions of Organotin Reagents with Organic Electrophiles [New Synthetic Methods (58)]. Angewandte Chemie International Edition in English. https://doi.org/10.1002/anie.198605081

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.