Hydrozirconation of Stannylacetylenes: A Novel and Highly Efficient Synthesis of 1,1-Diiodo-, 1,1-Dibromo-, and Mixed (Z)- or (E)-1-Iodo-1-bromo-1-alkenes Using 1,1-Hetero-Bimetallic Reagents-Reference-Cited by-同舟云学术

Hydrozirconation of Stannylacetylenes: A Novel and Highly Efficient Synthesis of 1,1-Diiodo-, 1,1-Dibromo-, and Mixed (Z)- or (E)-1-Iodo-1-bromo-1-alkenes Using 1,1-Hetero-Bimetallic Reagents

Published:2001-09-07 Issue:39 Volume:123 Page:9694-9695
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Dabdoub Miguel J.¹,Dabdoub Vânia B.¹,Baroni Adriano C. M.¹

Affiliation:

1. Laboratório de Síntese de Compostos Organocalcogênios Departamento de Química - FFCLRP Universidade de São Paulo, Av. Bandeirantes, 3900 Ribeirão Preto, São Paulo, Brazil

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja0114660

Reference24 articles.

1. Brominated unsaturated acids from the marine sponge .

2. A brominated bisacetylenic acid from the marine sponge

3. Selective debromination of 1,1-dibromoalkenes; a new access to Di- or trisubstituted alkenes

4. A remarkable steric effect in palladium-catalyzed Grignard coupling: regio- and stereoselective monoalkylation and -arylation of 1,1-dichloro-1-alkenes

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