Abstract
Abstract Synthesis of novel (3a,S)‐1‐aryl/aryloxy/alkoxy‐3a,4‐dihydro‐3H‐1λ5‐[1,3,2]oxazaphospholo [3,4‐a] indole‐1‐ones, thiones, and selenones was achieved in two steps with high yields from 2,3‐dihydro‐1H‐indol‐2(S)yl methanol (1) and dichlorophenyl phosphine/ethyl dichlorophosphite (2a and b) in the presence of triethylamine in dry THF followed by treatment with hydrogen peroxide, sulfur, and selenium. The compounds 4g–k have been synthesized by the direct cyclocondensation of 1 with different substituted phenyl phosphorodichloridates (2c–e, g) and bis(2‐chloroethyl) phosphoramidic dichloride (2f).
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