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Only two spinach herbicides are currently available to producers, and with limited choices in herbicide mode of action (MOA), overuse of the current herbicides can result in dominance of uncontrolled weeds. Therefore, spinach producers need more herbicide options. Trials were conducted in processing spinach to evaluate the crop safety of dimethenamid-p (0.56 kg ai/ha), EPTC (2.94 to 3.40 kg ai/ha), or ethofumesate (0.84, 1.12 or 2.24 kg ai/ha) applied pre-emergent (PRE), and ethofumesate (0.09 or 0.18 kg ai/ha) applied early postemergent (EPOST) for potential use as alternatives to s-metolachlor (0.73 kg ai/ha) and cycloate (2.52 kg ai/ha). The control of London rocket was excellent with s-metolachlor, dimethenamid-p, and ethofumesate. Weed control with cycloate and EPTC was fair, and generally inferior to all others. Cycloate and s-metolachlor were safe to spinach, and only minor crop injury was observed with all other herbicides, except the high rate of ethofumesate PRE, which resulted in high levels of...

Base-promoted cyclization of tert-butyl [2-(benzylideneamino)phenyl]acetate (13a) and subsequent C3-alkylation with allyl bromide affords 3-allyl-2-phenyl-2,3-dihydro-1H-indole-3-carboxylic acid, tert-butyl ester (15b) in high yield as a single diastereomer. This result is contrary to prior publications that describe failed cyclization of an analogous ethyl ester (ethyl [2-(4-methoxybenzylideneamino)phenyl]acetate) under strongly basic conditions. N-Acylation, olefin dihydroxylation, and tert-butyl ester cleavage affords the spirocyclic lactone 18 as a pair of diastereomers. Isolation and characterization of individual diastereomers 18a and 18b are described.

A synthesis of 6-amino-7-cyclohexyl-3,5-heptanediol 1 (CDH) and related amino 1,3-diols involving a nucleophilic ring opening of N-acyl activated lactams is described. Stereochemical proof of the 1,3-diol moiety is also presented.

Statine (STA, 8) and its cyclohexyl analog (ACHPA, 9) are obtained by a stereospecific synthesis via tetramic acid chemistry. Amides of STA and ACHPA, useful for the synthesis of antihyperten-sive renin inhibitors, are prepared directly from the intermediate activated lactams 7 by nucleophilic ring opening with amines.

The mass spectral fragmentation of a series of 10 mitosene analogs is described. Major pathways arise through decomposition of the substituents in the 1 and 10 positions and are unaffected by the substituent in the 7 position. The base peak in the spectrum, in most cases, is represented by the basic mitosene ring. The patterns are general for this series of compounds and may have application in elucidating the structure of the DNA alkylation sites involved in reactions with mitosenes or natural mitomycins.

Oxindole is converted to its dianion by treatment with two equivalents each of n-BuLi and TMEDA. Alkylations with a number of common electrophiles define the scope of synthetically useful transformations leading to 3-monosubstituted and 3,3-disubstituted oxindoles.