Facile chelation-controlled reductive opening of methoxybenzylidene acetals with Bu3SnH and MgBr2. Regioselective protection strategy as MPM ethers

Tetrahedron Letters

Volumn 41, Issue 33, 2000, Pages 6441-6445

  Zheng, B Z ^a   Yamauchi, M ^a   Dei, H ^a   Kusaka, S I ^a   Matsui, K ^a   Yonemitsu, O ^a  

^a OKAYAMA UNIVERSITY OF SCIENCE   (Japan)

Author keywords

Benzylidene acetal; Chelation; Magnesium bromide; Protecting group; Reductive cleavage; Regioselection; Tri n butyltin hydride

Indexed keywords

ACETAL DERIVATIVE; BENZYLIDENE DERIVATIVE; ETHER DERIVATIVE;

ARTICLE; CHELATION; CHEMICAL STRUCTURE; JAPAN; REDUCTION; SYNTHESIS;

EID: 0034641464     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)01017-0     Document Type: Article

References (32)