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1 f the polymerization is a tris-polymethylene organoborane.
2 ng but promising method for the synthesis of organoboranes.
3  are obtainable from the intermediate chiral organoboranes.
4  and atom-economic tool for the synthesis of organoboranes.
5 d for a highly enantioselective synthesis of organoboranes.
6  catalyst provided access to 16 novel chiral organoboranes.
7           We investigated the actions of the organoborane, 2-aminoethoxydiphenylborane (2APB), on Ca2
8 latoboryl nucleophile with the electrophilic organoboranes, 9-BBN and Ph3 B, provide facile B-B' sing
9 ifunctionalization of terminal alkynes using organoboranes and allylic carbonates as coupling partner
10 es or the transfer of special units from the organoboranes and represent a useful generalization of t
11                  The bifunctional conjugated organoboranes Ar2B-bt-BAr2, which contain 2,2'-bithiophe
12 ttractive endeavor, given that the resulting organoboranes are privileged synthons of utmost relevanc
13                         Even highly hindered organoboranes are quantitatively converted to their boro
14     The bonding in 1 and its reactivity with organoboranes are reminiscent of CO.
15                                              Organoboranes are some of the most synthetically valuabl
16          Remarkably, the reactivity of these organoboranes as inhibitors of autoxidation was shown to
17  aldol-type products directly using two-fold organoborane catalysis.
18                            Trialkyl and aryl organoboranes catalyze the polymerization of dimethylsul
19                                              Organoborane-catalyzed hydroboration of nitriles provide
20 aring almost any alkyl group available using organoborane chemistry and incorporating all features of
21 or the cross-coupling of formate esters with organoboranes, forming aldehydes under mild, additive-fr
22           The oxidation of these macrocyclic organoboranes generates a three-armed star polymethylene
23 n of 1-bromo and 1-chloroalkyl radicals from organoboranes has been investigated.
24 ctions of aryl-stabilized sulfur ylides with organoboranes has been studied under a variety of condit
25                                   Conjugated organoboranes have emerged as attractive hybrid material
26                                  These novel organoborane homoalanine anion equivalents are generated
27 tic potential of the expected functionalised organoboranes, however, many groups have recently focuse
28 ically encoded platform for producing chiral organoboranes in bacteria.
29 tion reactions provide direct access to aryl organoboranes, including aryl boronic esters.
30                The unique mechanism of these organoboranes is one of only a handful of RTA mechanisms
31 98:<2 site selectivity and furnish secondary organoborane isomers that complement those obtained thro
32 simple and intuitive matching of weak/strong organoborane LA and amine LB pairs offers access to a la
33 e homologation of phosphorus carbenoids with organoboranes leads to alpha-boranophosphorus compounds,
34 etermination of the isomeric distribution in organoborane mixtures resulting from common organoborane
35                               Representative organoborane mixtures were quantitatively converted to t
36  particular focus has been the generation of organoboranes, organosilanes and organostannanes from si
37 educing agents employed include organozincs, organoboranes, organosilanes, and methanol.
38 mologation reaction to cyclic and polycyclic organoboranes permits the construction of unique oligome
39  organoborane mixtures resulting from common organoborane processes (e.g., hydroboration).
40 meric composition of a variety of asymmetric organoborane processes.
41                                          The organoborane products are among the most versatile synth
42 be tuned to provide either enantiomer of the organoborane products.
43    Through this simple KH treatment, complex organoborane reaction mixtures are converted to the corr
44 al and straightforward route to these chiral organoborane reagents in one-pot has been developed alon
45 yde and ketone substrates using these chiral organoborane reagents in subsequent coupling reactions.
46                                              Organoborane reagents were investigated as coupling part
47 typal Lewis acids such that common routes to organoboranes rely on the reactivity of boron as an elec
48 ompete or possibly outperform the ubiquitous organoboranes, several groups, including ours, have enga
49  with pre-generated organozinc, Grignard and organoborane species has been used to furnish diverse mo
50 ferent approach toward highly functionalized organoborane synthesis by using recoverable ultrathin ca
51 d homolytic substitution (S(H)2) mechanisms, organoboranes that bear groups that can stabilize tetrac
52 rtunity for the development of new routes to organoboranes, the synthesis of current candidates is ge
53 ickel-catalyzed reaction with organozincs or organoboranes to afford densely functionalized cyclohexe
54  demonstrated by converting the intermediate organoboranes to alcohols, amines, and alkenes.
55 type reaction of imines, acid chlorides, and organoboranes to form alpha-substituted amides is descri
56                         Trialkyl and triaryl organoboranes undergo multiple, repetitive homologations
57 ccessible phosphorescence of heavy atom-free organoboranes via photochemical switching of sterically
58                               Representative organoboranes were examined by this new technique permit
59 thetic target of this method, polymeric star organoboranes with molecular weights of 1.5 million have
60                             The reactions of organoboranes with peroxyl radicals are key to their use
61 involves initial formation of a zwitterionic organoborane.ylide complex which breaks down in a rate-l