R-amino acid reductions, allow entry to other classes of compounds that are also useful as
the source of chiral centers, as with R-amino aldehydes, that, in turn, can be used in a …

The majority of bulk organic products contain oxygen functionalities. Many of these are
produced in chemical and petrochemical industries by direct oxyfunctionalization of …

This classical textbook in the best sense of the word is now completely revised, updated and
with more than 40% new content. The approved ordering system according to the ring size …

The availability of efficient methods for the con-struction of enantiopure a-hydroxy carbonyl
com-pounds [RR'C (0H) C (0) Z] is of considerable current interest because this structural …

This account reviews our efforts over the past 37 years to understand the chemistry of a
select group of sulfur− nitrogen compounds including sulfinimines (N-sulfinyl imines) and N …

Enantiomerically pure sulfinimines (thiooxime S-oxides 10), important building blocks in the
asymmetric synthesis of amine derivatives, are prepared in good to excellent yields in one …

The autoxidation of enolizable carbonyl compounds was reported as early as 1871, and the
accelerating action of base is well documented. The products of these reactions, however …

The synthesis and enantioselective oxidations of [(8, 8-dihalocamphoryl) sulfonyl]
oxaziridines [8, 8-dichlorol, 7, 7-trimethyl-2,-(phenylsulfonyl) spiro [bicyclo [2.2. 1] heptane-2 …

This comprehensive text presents a critical discussion of the scopes and limitations of
various organic synthetic methodologies that are available for performing asymmetric …

Three syntheses of the architecturally complex, cytotoxic marine macrolide (+)-spongistatin 1
(1) are reported. Highlights of the first-generation synthesis include: use of a dithiane …