Volume 26, Issue 19
Natural Products
Full Access

ChemInform Abstract: Efficient Cleavage of the Terminal Acetonide Group: Chirospecific Synthesis of 2,5-Dideoxy-2,5-imino-D-mannitol.

K. H. PARK

K. H. PARK

Dep. Chem., Gyeongsang Natl. Univ., Chinju 660-701, S. Korea,

Search for more papers by this author
Y. J. YOON

Y. J. YOON

Dep. Chem., Gyeongsang Natl. Univ., Chinju 660-701, S. Korea,

Search for more papers by this author
S. G. LEE

S. G. LEE

Dep. Chem., Gyeongsang Natl. Univ., Chinju 660-701, S. Korea,

Search for more papers by this author
First published: May 9, 1995

Abstract

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

ChemInform Abstract

A facile and efficient ion-exchange procedure to cleave selectively primary-secondary acetonide groups is described. This strategy is applied to a convenient synthesis of 2,5-dideoxy-2,5-imino-D-mannitol ( DMDP) (XI).

chemical structure image

    The full text of this article hosted at iucr.org is unavailable due to technical difficulties.